M. Bellesi, M. Pfister-genskow, S. Maret, S. Keles, G. Tononi et al., Effects of sleep and wake on oligodendrocytes and their precursors, Journal of Neuroscience, vol.33, issue.36, pp.14288-14300, 2013.

S. L. Bengtsson, Z. Nagy, S. Skare, L. Forsman, H. Forssberg et al., Extensive piano practicing has regionally specific effects on white matter development, Nature Neuroscience, vol.8, issue.9, p.1148, 2005.

M. Bennett, L. Farnell, and W. Gibson, A quantitative model of cortical spreading depression due to purinergic and gap-junction transmission in astrocyte networks, Biophys. J, vol.95, issue.12, pp.5648-5660, 2008.

B. Benz, G. Grima, and K. Q. Do, Glutamate-induced homocysteic acid release from astrocytes: possible implication in glia-neuron signaling, Neuroscience, vol.124, issue.2, pp.377-386, 2004.

Y. Bernardinelli, D. Muller, and I. Nikonenko, Astrocyte-synapse structural plasticity, Neural Plasticity, p.23215, 2014.

Y. Bernardinelli, J. Randall, E. Janett, I. Nikonenko, S. König et al., Activity-dependent structural plasticity of perisynaptic astrocytic domains promotes excitatory synapse stability, Current Biology, vol.24, issue.15, pp.1679-1688, 2014.

C. W. Berridge, Noradrenergic modulation of arousal, Brain Research Reviews, vol.58, issue.1, pp.1-17, 2008.

C. W. Berridge and B. D. Waterhouse, The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes, Brain Research Reviews, vol.42, issue.1, pp.33-84, 2003.

M. J. Berridge, P. Lipp, and M. D. Bootman, The versatility and universality of calcium signalling, Nat. Rev. Mol. Cell. Biol, vol.1, pp.11-21, 2000.

M. Berry, M. Ibrahim, J. Carlile, F. Ruge, A. Duncan et al., Axon-glial relationships in the anterior medullary velum of the adult rat, Journal of Neurocytology, vol.24, issue.12, pp.965-983, 1995.

P. Bezzi, M. Domercq, L. Brambilla, R. Galli, D. Schols et al., CXCR4-activated astrocyte glutamate release via TNF?: amplification by microglia triggers neurotoxicity, Nat. Neurosci, vol.4, issue.7, pp.702-710, 2001.

P. Bezzi and A. Volterra, A neuron-glia signalling network in the active brain, Curr. Opinion Neurobiol, vol.11, pp.387-394, 2001.

W. Bialek and F. Rieke, Reliability and information transmission in spiking neurons, Trends in Neurosciences, vol.15, issue.11, pp.428-434, 1992.

K. Biber, D. J. Laurie, A. Berthele, B. Sommer, T. R. Tölle et al., Expression and signaling of group i metabotropic glutamate receptors in astrocytes and microglia, Journal of Neurochemistry, vol.72, issue.4, pp.1671-1680, 1999.

E. Bienenstock, L. Cooper, and P. Munro, Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex, J. Neurosci, vol.2, issue.1, pp.32-48, 1982.

E. Bindocci, I. Savtchouk, N. Liaudet, D. Becker, G. Carriero et al., , 2017.

, Three-dimensional Ca 2+ imaging advances understanding of astrocyte biology, Science, vol.356, p.6339

T. E. Bjorness, N. Dale, G. Mettlach, A. Sonneborn, B. Sahin et al., An adenosine-mediated glial-neuronal circuit for homeostatic sleep, Journal of Neuroscience, vol.36, issue.13, pp.3709-3721, 2016.

C. Bonansco, A. Couve, G. Perea, C. A. Ferradas, M. Roncagliolo et al., Glutamate released spontaneously from astrocytes sets the threshold for synaptic plasticity, Eur. J. Neurosci, vol.33, pp.1483-1492, 2011.

J. G. Borst and B. Sakmann, Effect of changes in action potential shape on calcium currents and transmitter release in a calyx-type synapse of the rat auditory brainstem, Philosophical Transactions of the Royal Society of London B: Biological Sciences, vol.354, pp.347-355, 1381.

S. Boudkkazi, L. Fronzaroli-molinieres, D. , and D. , Presynaptic action potential waveform determines cortical synaptic latency, The Journal of Physiology, vol.589, issue.5, pp.1117-1131, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01766839

C. W. Bourque and L. P. Renaud, Electrophysiology of mammalian magnocellular vasopressin and oxytocin neurosecretory neurons, Frontiers in Neuroendocrinology, vol.11, issue.3, pp.183-212, 1990.

A. Bouzier-sore and L. Pellerin, Unraveling the complex metabolic nature of astrocytes, Frontiers in Cellular Neuroscience, vol.7, p.179, 2013.

D. N. Bowser and B. S. Khakh, Vesicular ATP is the predominant cause of intercellular calcium waves in astrocytes, J. Gen. Physiol, vol.129, issue.6, pp.485-491, 2007.

J. Brea, W. Senn, and J. Pfister, Matching recall and storage in sequence learning with spiking neural networks, The Journal of Neuroscience, vol.33, issue.23, pp.9565-9575, 2013.

D. V. Buonomano and M. M. Merzenich, Cortical plasticity: from synapses to maps. Annual review of neuroscience, vol.21, pp.149-186, 1998.

E. A. Bushong, M. E. Martone, Y. Z. Jones, and M. H. Ellisman, Protoplasmic astrocyte in CA1 stratum radiatum occupy separate anatomical domains, J. Neurosci, vol.22, issue.1, pp.183-192, 2002.

A. M. Butt, Neurotransmitter-mediated calcium signalling in oligodendrocyte physiology and pathology, Glia, vol.54, issue.7, pp.666-675, 2006.

A. M. Butt, Neuroglia, chapter Structure and function of oligodendrocytes, pp.62-73, 2013.

A. M. Butt, M. Ibrahim, and M. Berry, Axon-myelin sheath relations of oligodendrocyte unit phenotypes in the adult rat anterior medullary velum, J. Neurocytol, vol.27, issue.4, pp.259-269, 1998.

A. M. Butt, M. Pugh, P. Hubbard, J. , and G. , Functions of optic nerve glia: axoglial signalling in physiology and pathology, Eye, vol.18, issue.11, p.1110, 2004.

G. Buzsáki, Neural syntax: cell assemblies, synapsembles, and readers, Neuron, vol.68, issue.3, pp.362-385, 2010.

G. Buzsáki and A. Draguhn, Neuronal oscillations in cortical networks, Science, vol.304, issue.5679, pp.1926-1929, 2004.

D. Calvetti and E. Somersalo, Dynamic activation model for a glutamatergic neurovascular unit, Journal of Theoretical Biology, vol.274, issue.1, pp.12-29, 2011.

D. Calvetti and E. Somersalo, Ménagè a trois: the role of neurotransmitters in the energy metabolism of astrocytes, glutamatergic, and GABAergic neurons, Journal of Cerebral Blood Flow & Metabolism, vol.32, issue.8, pp.1472-1483, 2012.

M. A. Carmona, K. K. Murai, L. Wang, A. J. Roberts, P. et al., Glial ephrin-A3 regulates hippocampal dendritic spine morphology and glutamate transport, Proceedings of the National Academy of Sciences, vol.106, issue.30, pp.12524-12529, 2009.

C. E. Carr and M. Konishi, A circuit for detection of interaural time differences in the brain stem of the barn owl, Journal of Neuroscience, vol.10, issue.10, pp.3227-3246, 1990.

C. E. Carr and D. Soares, Evolutionary convergence and shared computational principles in the auditory system, Brain, Behavior and Evolution, vol.59, issue.5-6, pp.294-311, 2002.

C. E. Carr, D. Soares, S. Parameshwaran, P. , and T. , Evolution and development of time coding systems, Current Opinion in Neurobiology, vol.11, issue.6, pp.727-733, 2001.

M. A. Castro, F. A. Beltrán, S. Brauchi, C. , and I. I. , A metabolic switch in brain: glucose and lactate metabolism modulation by ascorbic acid, Journal of neurochemistry, vol.110, issue.2, pp.423-440, 2009.

T. I. Chao, M. Rickmann, and J. R. Wolff, The synapse-astrocyte boundary: an anatomical basis for an integrative role of glia in synaptic transmission, The Tripartite Synapse: Glia in Synaptic Transmission, pp.3-23, 2002.

N. Chen, H. Sugihara, J. Sharma, G. Perea, J. Petravicz et al., Nucleus basalis enabled stimulus specific plasticity in the visual cortex is mediated by astrocytes, Proc. Natl. Acad. Sci. USA, vol.109, issue.41, pp.2832-2841, 2012.

M. Chesler, Regulation and modulation of ph in the brain, Physiological Reviews, vol.83, issue.4, pp.1183-1221, 2003.

O. Chever, B. Djukic, K. D. Mccarthy, A. , and F. , Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knockout mice, Journal of Neuroscience, vol.30, issue.47, pp.15769-15777, 2010.

O. Chever, U. Pannasch, P. Ezan, R. , and N. , Astroglial connexin 43 sustains glutamatergic synaptic efficacy, Phil. Trans. R. Soc. B, vol.369, p.20130596, 1654.

L. Churchill, D. M. Rector, K. Yasuda, C. Fix, M. J. Rojas et al., Tumor necrosis factor ?: activity dependent expression and promotion of cortical column sleep in rats, Neuroscience, vol.156, issue.1, pp.71-80, 2008.

C. Cirelli, C. M. Gutierrez, and G. Tononi, Extensive and divergent effects of sleep and wakefulness on brain gene expression, Neuron, vol.41, issue.1, pp.35-43, 2004.

L. E. Clarke and B. A. Barres, Emerging roles of astrocytes in neural circuit development, Nature Reviews Neuroscience, vol.14, issue.5, pp.311-321, 2013.

J. D. Clements, Transmitter timecourse in the synaptic cleft: its role in central synaptic function, Trends Neurosci, vol.19, issue.5, pp.163-171, 1996.

S. Coco, F. Calegari, E. Pravettoni, D. Pozzi, E. Taverna et al., Storage and release of ATP from astrocytes in culture, J. Biol. Chem, vol.278, issue.2, pp.1354-1362, 2003.

J. A. Colombo, W. Härtig, S. Lipina, and N. Bons, Astroglial interlaminar processes in the cerebral cortex of prosimians and Old World monkeys, Anatomy and embryology, vol.197, issue.5, pp.369-376, 1998.

J. A. Colombo and H. D. Reisin, Interlaminar astroglia of the cerebral cortex: a marker of the primate brain, Brain research, vol.1006, issue.1, pp.126-131, 2004.

S. Condamine, R. Lavoie, D. Verdier, and A. Kolta, Functional rhythmogenic domains defined by astrocytic networks in the trigeminal main sensory nucleus, Glia, vol.66, issue.2, pp.311-326, 2018.

A. H. Cornell-bell, S. M. Finkbeiner, M. S. Cooper, and S. J. Smith, Glutamate induces calcium waves in cultured astrocytes: long-range glial signaling, Science, vol.247, issue.4941, pp.470-473, 1990.

A. Covelo and A. Araque, Neuronal activity determines distinct gliotransmitter release from a single astrocyte, eLife, vol.7, p.32237, 2018.

Y. Cui, Y. Yang, Z. Ni, Y. Dong, G. Cai et al., Astroglial Kir4.1 in the lateral habenula drives neuronal bursts in depression, Nature, vol.554, issue.7692, p.323, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01683191

R. Cunhaa and J. Ribeiro, ATP as a presynaptic modulator, Life Sciences, vol.68, pp.119-137, 2000.

D. Ambrosio, R. Gordon, D. S. , W. , and H. R. , Differential role of KIR channel and Na + /K +-pump in the regulation of extracellular K + in rat hippocampus, Journal of Neurophysiology, vol.87, issue.1, pp.87-102, 2002.

N. C. Danbolt, Glutamate uptake, Progress Neurobiol, vol.65, pp.1-105, 2001.

N. C. Danbolt, K. P. Lehre, Y. Dehnes, and K. Ullensvang, Transporters for synaptic transmitter on the glial cell plasma membrane, The Tripartite Synapse: Glia in Synaptic Transmission, pp.47-61, 2002.

J. W. Dani, A. Chernjavsky, and S. J. Smith, Neuronal activity triggers calcium waves in hippocampal astrocyte networks, Neuron, vol.8, pp.429-440, 1992.

M. De-pittà and N. Brunel, Modulation of synaptic plasticity by glutamatergic gliotransmission: A modeling study, Neural Plasticity, p.7607924, 2016.

M. De-pittà, N. Brunel, and A. Volterra, Astrocytes: orchestrating synaptic plasticity? Neuroscience, 2015.

M. De-pittà, M. Goldberg, V. Volman, H. Berry, B. et al., Glutamatedependent intracellular calcium and IP 3 oscillating and pulsating dynamics in astrocytes, J. Biol. Phys, vol.35, pp.383-411, 2009.

C. Frisch, M. Theis, D. Souza-silva, M. A. Dere, E. Söhl et al., Mice with astrocyte-directed inactivation of connexin43 exhibit increased exploratory behaviour, impaired motor capacities, and changes in brain acetylcholine levels, European Journal of Neuroscience, vol.18, issue.8, pp.2313-2318, 2003.

R. C. Froemke and Y. Dan, Spike-timing-dependent synaptic modification induced by natural spike trains, Nature, vol.416, issue.6879, pp.433-438, 2002.

R. C. Froemke, D. Debanne, and G. Bi, Temporal modulation of spike-timingdependent plasticity. Frontiers in synaptic neuroscience, vol.2, pp.1-16, 2010.

R. C. Froemke, I. A. Tsay, M. Raad, J. D. Long, D. et al., Contribution of individual spikes in burst-induced long-term synaptic modification, Journal of Neurophysiology, vol.95, issue.3, pp.1620-1629, 2006.

C. Frühbeis, D. Fröhlich, W. P. Kuo, J. Amphornrat, S. Thilemann et al., Neurotransmitter-triggered transfer of exosomes mediates oligodendrocyte-neuron communication, PLoS Biology, vol.11, issue.7, p.1001604, 2013.

S. Funahashi, C. J. Bruce, and P. S. Goldman-rakic, Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex, Journal of Neurophysiology, vol.61, issue.2, pp.331-349, 1989.

E. Ganmor, R. Segev, and E. Schneidman, A thesaurus for a neural population code. eLife, vol.4, p.6134, 2015.

A. Garnier, A. Vidal, and H. Benali, A theoretical study on the role of astrocytic activity in neuronal hyperexcitability by a novel neuron-glia mass model, The Journal of Mathematical Neuroscience, vol.6, issue.1, p.10, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01213918

W. Gerstner and W. M. Kistler, Mathematical formulations of Hebbian learning, Biological Cybernetics, vol.87, issue.5-6, pp.404-415, 2002.

C. Giaume, A. Koulakoff, L. Roux, D. Holcman, R. et al., Astroglial networks: a step further in neuroglial and gliovascular interactions, Nat. Rev. Neurosci, vol.11, issue.2, pp.87-99, 2010.

M. E. Gibbs, B. S. O'dowd, L. Hertz, S. R. Robinson, G. L. Sedman et al., Inhibition of glutamine synthetase activity prevents memory consolidation, Cognitive Brain Research, vol.4, issue.1, pp.57-64, 1996.

A. G. Gilman, G proteins: transducers of receptor-generated signals, Annual Review of Biochemistry, vol.56, issue.1, pp.615-649, 1987.

L. Goldman and J. S. Albus, Computation of impulse conduction in myelinated fibers; theoretical basis of the velocity-diameter relation, Biophysical Journal, vol.8, issue.5, pp.596-607, 1968.

P. S. Goldman-rakic, Cellular basis of working memory, Neuron, vol.14, issue.3, pp.477-485, 1995.

G. Gordon, D. Baimoukhametova, S. Hewitt, W. Rajapaksha, T. Fisher et al., Norepinephrine triggers release of glial ATP to increase postsynaptic efficacy, Nat. Neurosci, vol.8, issue.8, pp.1078-1086, 2005.

G. R. Gordon, H. B. Choi, R. L. Rungta, G. C. Ellis-davies, and B. A. Macvicar, Brain metabolism dictates the polarity of astrocyte control over arterioles, Nature, vol.456, issue.7223, p.745, 2008.

G. R. Gordon, S. J. Mulligan, and B. A. Macvicar, Astrocyte control of the cerebrovasculature, Glia, vol.55, issue.12, pp.1214-1221, 2007.

M. Götz, Neuroglia, chapter Radial glial cells, pp.50-61, 2013.

A. V. Gourine, V. Kasymov, N. Marina, F. Tang, M. F. Figueiredo et al., Astrocytes control breathing through ph-dependent release of ATP, Science, vol.329, issue.5991, pp.571-575, 2010.

M. Graupner and N. Brunel, Mechanisms of induction and maintenance of spike-timing dependent plasticity in biophysical synapse models, Frontiers in Computational Neuroscience, vol.4, issue.136, pp.1-19, 2010.

J. Grosche, H. Kettenmann, and A. Reichenbach, Bergmann glial cells form distinct morphological structures to interact with cerebellar neurons, J. Neurosci. Res, vol.68, pp.128-149, 2002.

J. Grosche, V. Matyash, T. Möller, A. Verkhratsky, A. Reichenbach et al., Microdomains for neuron-glia interaction: parallel fiber signaling to bergmann glial cells, Nature, vol.2, issue.2, pp.139-143, 1999.

R. Gruetter, Glycogen: the forgotten cerebral energy store, Journal of Neuroscience Research, vol.74, issue.2, pp.179-183, 2003.

J. J. Guinan, B. E. Norris, and S. S. Guinan, Single auditory units in the superior olivary complex: II: locations of unit categories and tonotopic organization, International Journal of Neuroscience, vol.4, issue.4, pp.147-166, 1972.

S. Habbas, M. Santello, D. Becker, H. Stubbe, G. Zappia et al., Neuroinflammatory TNF? impairs memory via astrocyte signaling, Cell, vol.163, issue.7, pp.1730-1741, 2015.

M. Haber, L. Zhou, and K. K. Murai, Cooperative astrocyte and dendritic spine dynamics at hippocampal excitatory synapses, J. Neurosci, vol.26, issue.35, pp.8881-8891, 2006.
DOI : 10.1523/jneurosci.1302-06.2006

M. Halassa and P. Haydon, Integrated brain circuits: astrocytic networks modulate neuronal activity and behavior, Annu. Rev. Physiol, vol.72, pp.335-355, 2010.

M. M. Halassa, T. Fellin, H. Takano, J. Dong, H. et al., Synaptic islands defined by the territory of a single astrocyte, J. Neurosci, vol.27, issue.24, pp.6473-6477, 2007.

M. M. Halassa, C. Florian, T. Fellin, J. R. Munoz, S. Y. Lee et al., Astrocytic modulation of sleep homeostasis and cognitive consequences of sleep loss, Neuron, vol.61, issue.2, pp.213-219, 2009.

J. A. Halter, C. , and J. W. , A distributed-parameter model of the myelinated nerve fiber, Journal of Theoretical Biology, vol.148, issue.3, pp.345-382, 1991.

N. Hamilton, S. Vayro, F. Kirchhoff, A. Verkhratsky, J. Robbins et al., Mechanisms of ATP-and glutamate-mediated calcium signaling in white matter astrocytes, Glia, vol.56, issue.7, pp.734-749, 2008.

J. Han, P. Kesner, M. Metna-laurent, T. Duan, L. Xu et al., Acute cannabinoids impair working memory through astroglial CB 1 receptor modulation of hippocampal LTD, Cell, vol.148, issue.5, pp.1039-1050, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01160047

X. Han, M. Chen, F. Wang, M. Windrem, S. Wang et al., , 2013.

, Forebrain engraftment by human glial progenitor cells enhances synaptic plasticity and learning in adult mice, Cell Stem Cell, vol.12, issue.3, pp.342-353

B. J. Hansen, M. I. Chelaru, and V. Dragoi, Correlated variability in laminar cortical circuits, Neuron, vol.76, issue.3, pp.590-602, 2012.

J. J. Harris, R. Jolivet, A. , and D. , Synaptic energy use and supply, Neuron, vol.75, issue.5, pp.762-777, 2012.
DOI : 10.1016/j.neuron.2012.08.019

URL : https://doi.org/10.1016/j.neuron.2012.08.019

J. K. Harrison, Y. Jiang, S. Chen, Y. Xia, D. Maciejewski et al., Role for neuronally derived fractalkine in mediating interactions between neurons and CX3CR1-expressing microglia, Proceedings of the National Academy of Sciences, vol.95, issue.18, pp.10896-10901, 1998.

D. K. Hartline, The evolutionary origins of glia, Glia, vol.59, issue.9, pp.1215-1236, 2011.

P. G. Haydon, Glia: listening and talking to the synapse, Nat. Rev. Neurosci, vol.2, pp.185-193, 2001.

P. G. Haydon and G. Carmignoto, Astrocyte control of synaptic transmission and neurovascular coupling, Physiol. Rev, vol.86, pp.1009-1031, 2006.

L. Héja, P. Barabás, G. Nyitrai, K. A. Kékesi, B. Lasztóczi et al., Glutamate uptake triggers transporter-mediated GABA release from astrocytes, PloS One, vol.4, issue.9, p.7153, 2009.

L. Héja, G. Nyitrai, O. Kékesi, ´. A. Dobolyi, P. Szabó et al., Astrocytes convert network excitation to tonic inhibition of neurons, BMC Biology, vol.10, issue.1, p.26, 2012.

J. P. Heller and D. A. Rusakov, Morphological plasticity of astroglia: understanding synaptic microenvironment, Glia, vol.63, issue.12, pp.2133-2151, 2015.

C. Henneberger, T. Papouin, S. H. Oliet, and D. A. Rusakov, Long-term potentiation depends on release of D-serine from astrocytes, Nature, vol.463, pp.232-237, 2010.

S. Herculano-houzel, Not all brains are made the same: new views on brain scaling in evolution, Brain, Behavior and Evolution, vol.78, issue.1, pp.22-36, 2011.

S. Herculano-houzel, The glia/neuron ratio: how it varies uniformly across brain structures and species and what that means for brain physiology and evolution, Glia, vol.62, issue.9, pp.1377-1391, 2014.

J. L. Herrero, M. J. Roberts, L. S. Delicato, M. A. Gieselmann, P. Dayan et al., Acetylcholine contributes through muscarinic receptors to attentional modulation in v1, Nature, issue.7208, p.1110, 2008.

C. S. Herrmann, I. Fründ, and D. Lenz, Human gamma-band activity: a review on cognitive and behavioral correlates and network models, Neuroscience & Biobehavioral Reviews, vol.34, issue.7, pp.981-992, 2010.

C. S. Herrmann, M. H. Munk, and A. K. Engel, Cognitive functions of gamma-band activity: memory match and utilization, Trends in Cognitive Sciences, vol.8, issue.8, pp.347-355, 2004.

L. Hertz, Possible role of neuroglia: a potassium-mediated neuronal-neuroglial-neuronal impulse transmission system, Nature, vol.206, issue.4989, p.1091, 1965.

L. Hertz, Intercellular metabolic compartmentation in the brain: past, present and future, Neurochemistry International, vol.45, issue.2-3, pp.285-296, 2004.

L. Hertz, The glutamate-glutamine (GABA) cycle: importance of late postnatal development and potential reciprocal interactions between biosynthesis and degradation, Frontiers in Endocrinology, vol.4, p.59, 2013.

L. Hertz, L. Peng, and G. A. Dienel, Energy metabolism in astrocytes: high rate of oxidative metabolism and spatiotemporal dependence on glycolysis/glycogenolysis, Journal of Cerebral Blood Flow & Metabolism, vol.27, issue.2, pp.219-249, 2007.

H. Hirase, L. Qian, P. Barthó, and G. Buzsáki, Calcium dynamics of cortical astrocytic networks in vivo, PLoS Biol, vol.2, issue.4, pp.494-0496, 2004.

A. Hoffmann, O. Kann, C. Ohlemeyer, U. Hanisch, and H. Kettenmann, Elevation of basal intracellular calcium as a central element in the activation of brain macrophages (microglia): suppression of receptor-evoked calcium signaling and control of release function, Journal of Neuroscience, vol.23, issue.11, pp.4410-4419, 2003.

T. M. Hoogland, B. Kuhn, W. Göbel, W. Huang, J. Nakai et al., Radially expanding transglial calcium waves in the intact cerebellum, Proceedings of the National Academy of Sciences, vol.106, issue.9, pp.3496-3501, 2009.

B. M. Hooks and C. Chen, Distinct roles for spontaneous and visual activity in remodeling of the retinogeniculate synapse, Neuron, vol.52, issue.2, pp.281-291, 2006.

M. Hoshiko, I. Arnoux, E. Avignone, N. Yamamoto, A. et al., Deficiency of the microglial receptor CX3CR1 impairs postnatal functional development of thalamocortical synapses in the barrel cortex, Journal of Neuroscience, vol.32, issue.43, pp.15106-15111, 2012.

C. Howarth, P. Gleeson, A. , and D. , Updated energy budgets for neural computation in the neocortex and cerebellum, Journal of Cerebral Blood Flow & Metabolism, vol.32, issue.7, pp.1222-1232, 2012.

Y. Hu, J. Zylberberg, and E. Shea-brown, The sign rule and beyond: boundary effects, flexibility, and noise correlations in neural population codes, PLoS Computational Biology, vol.10, issue.2, p.1003469, 2014.

J. Y. Hua and S. J. Smith, Neural activity and the dynamics of central nervous system development, Nature Neuroscience, vol.7, issue.4, p.327, 2004.

Y. H. Huang and D. E. Bergles, Glutamate transporters bring competition to the synapse, Current Opinion in Neurobiology, vol.14, issue.3, pp.346-352, 2004.

E. G. Hughes, J. L. Orthmann-murphy, A. J. Langseth, and D. E. Bergles, Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex, Nature Neuroscience, vol.21, pp.696-706, 2018.
DOI : 10.1038/s41593-018-0121-5

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920726

C. Iadecola and M. Nedergaard, Glial regulation of the cerebral microvasculature, Nature Neuroscience, vol.10, issue.11, pp.1369-1376, 2007.

L. Imeri and M. R. Opp, How (and why) the immune system makes us sleep, Nature Reviews Neuroscience, vol.10, issue.3, p.199, 2009.
DOI : 10.1038/nrn2576

URL : https://air.unimi.it/bitstream/2434/54609/2/Imeri_NRN_mar09.pdf

Y. Imura, Y. Morizawa, R. Komatsu, K. Shibata, Y. Shinozaki et al., Microglia release ATP by exocytosis, Glia, issue.8, pp.1320-1330, 2013.
DOI : 10.1002/glia.22517

A. M. Ingiosi, M. R. Opp, and J. M. Krueger, Sleep and immune function: glial contributions and consequences of aging, Current Opinion in Neurobiology, vol.23, issue.5, pp.806-811, 2013.
DOI : 10.1016/j.conb.2013.02.003

URL : http://europepmc.org/articles/pmc3695049?pdf=render

T. Ishibashi, K. A. Dakin, B. Stevens, P. R. Lee, S. V. Kozlov et al., Astrocytes promote myelination in response to electrical impulses, Neuron, vol.49, issue.6, pp.823-832, 2006.
DOI : 10.1016/j.neuron.2006.02.006

URL : https://doi.org/10.1016/j.neuron.2006.02.006

I. Ismailov, D. Kalikulov, T. Inoue, and M. J. Friedlander, The kinetic profile of intracellular calcium predicts long-term potentiation and long-term depression, The Journal of Neuroscience, vol.24, issue.44, pp.9847-9861, 2004.
DOI : 10.1523/jneurosci.0738-04.2004

J. Israel, G. Le-masson, D. T. Theodosis, and D. A. Poulain, Glutamatergic input governs periodicity and synchronization of bursting activity in oxytocin neurons in hypothalamic organotypic cultures, European Journal of Neuroscience, vol.17, issue.12, pp.2619-2629, 2003.

E. M. Izhikevich, Polychronization: computation with spikes, Neural Computation, vol.18, issue.2, pp.245-282, 2006.
DOI : 10.1162/089976606775093882

F. R. Jackson, Glial cell modulation of circadian rhythms, Glia, vol.59, issue.9, pp.1341-1350, 2011.
DOI : 10.1002/glia.21097

URL : http://europepmc.org/articles/pmc3156034?pdf=render

A. P. Jadhav, K. Roesch, and C. L. Cepko, Development and neurogenic potential of müller glial cells in the vertebrate retina, Progress in retinal and eye research, vol.28, issue.4, pp.249-262, 2009.

L. F. Jaffe, Classes and mechanisms of calcium waves, Cell Calcium, vol.14, issue.10, pp.736-745, 1993.

S. D. Jeftinija, K. V. Jeftinija, G. Stefanovic, and F. Liu, Neuroligand-evoked calciumdependent release of excitatory amino acids from cultured astrocytes, J. Neurochem, vol.66, pp.676-684, 1996.
DOI : 10.1046/j.1471-4159.1996.66020676.x

P. Jiang, F. Xing, B. Guo, J. Yang, Z. Li et al., Nucleotide transmitters ATP and ADP mediate intercellular calcium wave communication via P2Y 12/13 receptors among BV-2 microglia, PloS one, vol.12, issue.8, p.183114, 2017.
DOI : 10.1371/journal.pone.0183114

URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0183114&type=printable

C. Jiménez-gonzález, T. Pirttimaki, D. W. Cope, and H. R. Parri, Non-neuronal, slow GABA signalling in the ventrobasal thalamus targets ?-subunit-containing GABA A receptors, European Journal of Neuroscience, vol.33, issue.8, pp.1471-1482, 2011.

S. Jinno, F. Fleischer, S. Eckel, V. Schmidt, and T. Kosaka, Spatial arrangement of microglia in the mouse hippocampus: a stereological study in comparison with astrocytes, Glia, vol.55, issue.13, pp.1334-1347, 2007.

D. Johnston, S. M. Wu, and .. , Foundations of cellular neurophysiology, 1995.

R. Jolivet, I. Allaman, L. Pellerin, P. J. Magistretti, W. et al., Comment on recent modeling studies of astrocyte-neuron metabolic interactions, Journal of Cerebral Blood Flow & Metabolism, vol.30, issue.12, pp.1982-1986, 2010.

P. X. Joris, L. H. Carney, P. H. Smith, Y. , and T. C. , Enhancement of neural synchronization in the anteroventral cochlear nucleus. I. Responses to tones at the characteristic frequency, Journal of neurophysiology, vol.71, issue.3, pp.1022-1036, 1994.

P. Jourdain, L. H. Bergersen, K. Bhaukaurally, P. Bezzi, M. Santello et al., Glutamate exocytosis from astrocytes controls synaptic strength, Nat. Neurosci, vol.10, issue.3, pp.331-339, 2007.
DOI : 10.1038/nn1849

A. Kadala, D. Verdier, P. Morquette, and A. Kolta, Ion homeostasis in rhythmogenesis: the interplay between neurons and astroglia, vol.30, pp.371-388, 2015.
DOI : 10.1152/physiol.00023.2014

URL : https://papyrus.bib.umontreal.ca/xmlui/bitstream/1866/19736/1/Kadala%20et%20al%202015_Physiology.pdf

K. Kaila, J. Voipio, P. Paalasmaa, M. Pasternack, and R. A. Deisz, The role of bicarbonate in GABA A receptor-mediated IPSPs of rat neocortical neurones, The Journal of Physiology, vol.464, issue.1, pp.273-289, 1993.

W. Kakegawa, Y. Miyoshi, K. Hamase, S. Matsuda, K. Matsuda et al., D-Serine regulates cerebellar LTD and motor coordination through the ?2 glutamate receptor, Nature Neuroscience, vol.14, issue.5, pp.603-611, 2011.
DOI : 10.1038/nn.2791

M. Kaneko, D. Stellwagen, R. C. Malenka, and M. P. Stryker, Tumor necrosis factoralpha mediates one component of competitive, experience-dependent plasticity in developing visual cortex, Neuron, vol.58, pp.673-680, 2008.

R. Káradóttir and D. Attwell, Neurotransmitter receptors in the life and death of oligodendrocytes, Neuroscience, vol.145, issue.4, pp.1426-1438, 2007.

M. Kaschube, M. Schnabel, S. Löwel, D. M. Coppola, L. E. White et al., Universality in the evolution of orientation columns in the visual cortex, Science, vol.330, issue.6007, pp.1113-1116, 2010.

N. Kasthuri, K. .. Hayworth, D. R. Berger, R. L. Schalek, J. A. Conchello et al., Saturated reconstruction of a volume of neocortex, Cell, vol.162, issue.3, pp.648-661, 2015.

H. Katagiri, K. Tanaka, M. , and T. , Requirement of appropriate glutamate concentrations in the synaptic cleft for hippocampal LTP induction, European Journal of Neuroscience, vol.14, issue.3, pp.547-553, 2001.

B. Katz, The release of neural transmitter substances, vol.10, 1969.

A. Keane and P. Gong, Propagating waves can explain irregular neural dynamics, Journal of Neuroscience, vol.35, issue.4, pp.1591-1605, 2015.
DOI : 10.1523/jneurosci.1669-14.2015

URL : http://www.jneurosci.org/content/35/4/1591.full.pdf

H. Kettenmann, U. Hanisch, M. Noda, and A. Verkhratsky, Physiology of microglia, Physiological Reviews, vol.91, issue.2, pp.461-553, 2011.

H. Kettenmann, F. Kirchhoff, and A. Verkhratsky, Microglia: new roles for the synaptic stripper, Neuron, vol.77, issue.1, pp.10-18, 2013.
DOI : 10.1016/j.neuron.2012.12.023

URL : https://doi.org/10.1016/j.neuron.2012.12.023

H. Kettenmann and B. R. Ransom, Neuroglia, The concept of neuroglia: A historical perspective, 2004.
DOI : 10.1093/acprof:oso/9780195152227.003.0001

H. Kettenmann and B. R. Ransom, Neuroglia, 2013.

B. S. Khakh and M. V. Sofroniew, Diversity of astrocyte functions and phenotypes in neural circuits, Nature Neuroscience, vol.18, issue.7, p.942, 2015.

P. J. Khandelwal, A. M. Herman, C. E. Moussa, and .. , Inflammation in the early stages of neurodegenerative pathology, Journal of neuroimmunology, vol.238, issue.1, pp.1-11, 2011.

F. Kimura and C. Itami, Myelination and isochronicity in neural networks, Frontiers in Neuroanatomy, vol.3, p.12, 2009.

G. A. Kinney and W. J. Spain, Synaptically evoked GABA transporter currents in neocortical glia, Journal of Neurophysiology, vol.88, issue.6, pp.2899-2908, 2002.

J. P. Kinney, J. Spacek, T. M. Bartol, C. L. Bajaj, K. M. Harris et al., Extracellular sheets and tunnels modulate glutamate diffusion in hippocampal neuropil, Journal of Comparative Neurology, vol.521, issue.2, pp.448-464, 2013.

Z. F. Kisvárday, E. Toth, M. Rausch, and U. T. Eysel, Orientation-specific relationship between populations of excitatory and inhibitory lateral connections in the visual cortex of the cat, Cerebral cortex, vol.7, issue.7, pp.605-618, 1997.

I. Klinkenberg, A. Sambeth, and A. Blokland, Acetylcholine and attention, Behavioural Brain Research, vol.221, issue.2, pp.430-442, 2011.

H. Ko, S. B. Hofer, B. Pichler, K. A. Buchanan, P. J. Sjöström et al., Functional specificity of local synaptic connections in neocortical networks, Nature, vol.473, issue.7345, p.87, 2011.

P. Kofuji and E. A. Newman, Potassium buffering in the central nervous system, Neuroscience, vol.129, issue.4, pp.1043-1054, 2004.

A. S. Kozlov, M. C. Angulo, E. Audinat, C. , and S. , Target cell-specific modulation of neuronal activity by astrocytes, Proc. Natl. Acad. Sci. USA, vol.103, issue.26, pp.10058-10063, 2006.

E. Krämer-albers, N. Bretz, S. Tenzer, C. Winterstein, W. Möbius et al., Oligodendrocytes secrete exosomes containing major myelin and stress-protective proteins: Trophic support for axons?, Proteomics-clinical applications, vol.1, issue.11, pp.1446-1461, 2007.

G. W. Kreutzberg, Microglia: a sensor for pathological events in the CNS, Trends in Neurosciences, vol.19, issue.8, pp.312-318, 1996.

B. Kriener, M. Helias, A. Aertsen, and S. Rotter, Correlations in spiking neuronal networks with distance dependent connections, Journal of Computational Neuroscience, vol.27, issue.2, pp.177-200, 2009.

M. Krzan, N. Stenovec, M. Kreft, T. Pangrsic, S. Grilc et al., Calcium-dependent exocytosis of atrial natriuretic peptide from astrocytes, J. Neurosci, vol.23, pp.1580-1583, 2003.

N. Kuga, T. Sasaki, Y. Takahara, N. Matsuki, and Y. Ikegaya, Large-scale calcium waves traveling through astrocytic networks in vivo, J. Neurosci, vol.31, issue.7, pp.2607-2614, 2011.

U. Kummer, L. F. Olsen, A. K. Green, E. Bomberg-bauer, and G. Baier, Switching from simple to complex oscillations in calcium signaling, Biophys. J, vol.79, pp.1188-1199, 2000.

A. M. Labin and E. N. Ribak, Retinal glial cells enhance human vision acuity, Physical Review Letters, vol.104, issue.15, p.158102, 2010.

A. M. Labin, S. K. Safuri, E. N. Ribak, P. , and I. , Müller cells separate between wavelengths to improve day vision with minimal effect upon night vision, Nature Communications, vol.5, p.4319, 2014.

E. J. Lang and J. Rosenbluth, Role of myelination in the development of a uniform olivocerebellar conduction time, Journal of Neurophysiology, vol.89, issue.4, pp.2259-2270, 2003.

B. R. Larsen, M. Assentoft, M. L. Cotrina, S. Z. Hua, M. Nedergaard et al., Contributions of the Na + /K +-ATPase, NKCC1, and Kir4.1 to hippocampal K + clearance and volume responses, Glia, vol.62, issue.4, pp.608-622, 2014.

S. B. Laughlin, Energy as a constraint on the coding and processing of sensory information, Current Opinion in Neurobiology, vol.11, issue.4, pp.475-480, 2001.

S. B. Laughlin and T. J. Sejnowski, Communication in neuronal networks, Science, vol.301, issue.5641, pp.1870-1874, 2003.

L. J. Lawson, V. H. Perry, P. Dri, G. , and S. , Heterogeneity in the distribution and morphology of microglia in the normal adult mouse brain, Neuroscience, vol.39, issue.1, pp.151-170, 1990.

L. Meur, K. Mendizabal-zubiaga, J. Grandes, P. , A. et al., GABA release by hippocampal astrocytes, Front. Comp. Neurosci, vol.6, 2012.

H. S. Lee, A. Ghetti, A. Pinto-duarte, X. Wang, G. Dziewczapolski et al., Astrocytes contribute to gamma oscillations and recognition memory, Proc. Nat. Acad. Sci. USA, pp.3343-3352, 2014.

M. Lee, E. G. Mcgeer, and P. L. Mcgeer, Mechanisms of GABA release from human astrocytes, Glia, vol.59, pp.1600-1611, 2011.

S. Lee, B. Yoon, K. Berglund, S. Oh, H. Park et al., Channel-mediated tonic GABA release from glia, Sci. STKE, vol.330, issue.6005, pp.790-796, 2010.

K. P. Lehre and D. A. Rusakov, Asymmetry of glia near central synapses favors presynaptically directed glutamate escape, Biophys. J, vol.83, issue.1, pp.125-134, 2002.

L. M. Levy, O. Warr, A. , and D. , Stoichiometry of the glial glutamate transporter GLT-1 expressed inducibly in a chinese hamster ovary cell line selected for low endogenous Na +-dependent glutamate uptake, Journal of Neuroscience, vol.18, issue.23, pp.9620-9628, 1998.

G. M. Lewitus, S. C. Konefal, A. D. Greenhalgh, H. Pribiag, K. Augereau et al., Microglial TNF-? suppresses cocaine-induced plasticity and behavioral sensitization, Neuron, vol.90, issue.3, pp.483-491, 2016.

G. M. Lewitus, H. Pribiag, R. Duseja, M. St-hilaire, and D. Stellwagen, An adaptive role of TNF? in the regulation of striatal synapses, Journal of Neuroscience, vol.34, issue.18, pp.6146-6155, 2014.

L. Leybaert and M. J. Sanderson, Intercellular Ca 2+ waves: mechanisms and function, Physiological reviews, vol.92, issue.3, pp.1359-1392, 2012.

B. L. Lind, A. R. Brazhe, S. B. Jessen, F. C. Tan, and M. J. Lauritzen, Rapid stimulus-evoked astrocyte Ca 2+ elevations and hemodynamic responses in mouse somatosensory cortex in vivo, Proceedings of the National Academy of Sciences, vol.110, issue.48, pp.4678-4687, 2013.

J. J. Lippman, T. Lordkipanidze, M. E. Buell, S. O. Yoon, and A. Dunaevsky, Morphogenesis and regulation of Bergmann glial processes during Purkinje cell dendritic spine ensheathment and synaptogenesis, Glia, vol.56, issue.13, pp.1463-1477, 2008.

J. J. Lippman, T. Lordkipanidze, N. Cobb, and A. Dunaevsky, Bergmann glial ensheathment of dendritic spines regulates synapse number without affecting spine motility, Neuron Glia Biology, vol.6, issue.3, pp.193-200, 2010.

A. Litwin-kumar and B. Doiron, Slow dynamics and high variability in balanced cortical networks with clustered connections, Nature Neuroscience, vol.15, issue.11, p.1498, 2012.

G. J. Liu, A. Kalous, E. L. Werry, and M. R. Bennett, Purine release from spinal cord microglia after elevation of calcium by glutamate, Molecular Pharmacology, vol.70, issue.3, pp.851-859, 2006.

M. López-hidalgo, W. B. Hoover, and J. Schummers, Spatial organization of astrocytes in ferret visual cortex, Journal of Comparative Neurology, vol.524, issue.17, pp.3561-3576, 2016.

M. López-hidalgo, K. Salgado-puga, R. Alvarado-martínez, A. C. Medina, R. A. Prado-alcalá et al., Nicotine uses neuron-glia communication to enhance hippocampal synaptic transmission and long-term memory, PloS one, vol.7, issue.11, p.49998, 2012.

M. López-hidalgo and J. Schummers, Cortical maps: a role for astrocytes?, Current Opinion in Neurobiology, vol.24, pp.176-189, 2014.

G. Losi, L. Mariotti, C. , and G. , GABAergic interneuron to astrocyte signalling: a neglected form of cell communication in the brain, Phil. Trans. Royal Soc. B: Biological Sciences, vol.369, p.20130609, 1654.

R. L. Lowery, M. Tremblay, B. E. Hopkins, and A. K. Majewska, The microglial fractalkine receptor is not required for activity-dependent plasticity in the mouse visual system, Glia, vol.65, issue.11, pp.1744-1761, 2017.

E. Luders, P. M. Thompson, and A. W. Toga, The development of the corpus callosum in the healthy human brain, Journal of Neuroscience, vol.30, issue.33, pp.10985-10990, 2010.

I. Lundgaard, M. L. Lu, E. Yang, W. Peng, H. Mestre et al., Glymphatic clearance controls state-dependent changes in brain lactate concentration, Journal of Cerebral Blood Flow & Metabolism, vol.37, issue.6, pp.2112-2124, 2017.

I. Lushnikova, G. Skibo, D. Muller, and I. Nikonenko, Synaptic potentiation induces increased glial coverage of excitatory synapses in ca1 hippocampus, Hippocampus, vol.19, issue.8, pp.753-762, 2009.

S. E. Lutz, Y. Zhao, M. Gulinello, S. C. Lee, C. S. Raine et al., Deletion of astrocyte connexins 43 and 30 leads to a dysmyelinating phenotype and hippocampal CA1 vacuolation, Journal of Neuroscience, vol.29, issue.24, pp.7743-7752, 2009.

B. Ma, M. Xie, and M. Zhou, Bicarbonate efflux via GABA A receptors depolarizes membrane potential and inhibits two-pore domain potassium channels of astrocytes in rat hippocampal slices, Glia, vol.60, issue.11, pp.1761-1772, 2012.

B. Mackenzie and J. D. Erickson, Sodium-coupled neutral amino acid (System N/A) transporters of the SLC38 gene family. Pflügers Archiv.-Eur, J. Physiol, vol.447, issue.5, pp.784-795, 2004.

P. J. Magistretti and I. Allaman, A cellular perspective on brain energy metabolism and functional imaging, Neuron, vol.86, issue.4, pp.883-901, 2015.

P. J. Magistretti and J. Chatton, Relationship between L-glutamate-regulated intracellular Na + dynamics and ATP hydrolysis in astrocytes, Journal of Neural Transmission, vol.112, issue.1, pp.77-85, 2005.

P. J. Magistretti, J. H. Morrison, W. J. Shoemaker, V. Sapin, and F. E. Bloom, Vasoactive intestinal polypeptide induces glycogenolysis in mouse cortical slices: a possible regulatory mechanism for the local control of energy metabolism, Proceedings of the National Academy of Sciences, vol.78, issue.10, pp.6535-6539, 1981.

S. Mangia, M. Dinuzzo, F. Giove, A. Carruthers, I. A. Simpson et al., Response to comment on recent modeling studies of astrocyteneuron metabolic interactions: Much ado about nothing, Journal of Cerebral Blood Flow & Metabolism, vol.31, issue.6, pp.1346-1353, 2011.

J. Marchaland, C. Caì-i, S. M. Voglmaier, H. Li, R. Regazzi et al., Fast subplasma membrane Ca 2+ transients control exo-endocytosis of synaptic-like microvesicles in astrocytes, J. Neurosci, vol.28, issue.37, pp.9122-9132, 2008.

J. S. Marchant and I. Parker, Role of elementary Ca 2+ puffs in generating repetitive Ca 2+ oscillations, The EMBO Journal, vol.20, issue.1-2, pp.65-76, 2001.

H. Markram, J. Lübke, M. Frotscher, A. Roth, and B. Sakmann, Physiology and anatomy of synaptic connections between thick tufted pyramidal neurones in the developing rat neocortex, The Journal of Physiology, vol.500, issue.2, pp.409-440, 1997.

H. Markram, Y. Wang, and M. Tsodyks, Differential signaling via the same axon of neocortical pyramidal neurons, Proc. Natl. Acad. Sci. USA, vol.95, pp.5323-5328, 1998.

R. Martín, R. Bajo-grañeras, R. Moratalla, G. Perea, A. et al., Circuit-specific signaling in astrocyte-neuron networks in basal ganglia pathways, Science, vol.349, issue.6249, pp.730-734, 2015.

M. Mashimo, Y. Okubo, T. Yamazawa, M. Yamasaki, M. Watanabe et al., Inositol 1,4,5-trisphosphate signaling maintains the activity of glutamate uptake in Bergmann glia, European Journal of Neuroscience, vol.32, issue.10, pp.1668-1677, 2010.

R. H. Masland, The fundamental plan of the retina, Nature Neuroscience, vol.4, issue.9, p.877, 2001.

M. Matsuzaki, G. Ellis-davies, T. Nemoto, Y. Miyashita, M. Iino et al., Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons, Nat. Neurosci, vol.4, issue.11, pp.1086-1092, 2001.

V. Matyash and H. Kettenmann, Heterogeneity in astrocyte morphology and physiology, Brain Res. Rev, vol.63, issue.1-2, pp.2-10, 2010.

D. Mcalpine and B. Grothe, Sound localization and delay lines-do mammals fit the model?, Trends in Neurosciences, vol.26, issue.7, pp.347-350, 2003.

D. A. Mccormick, Y. Shu, A. Hasenstaub, M. Sanchez-vives, M. Badoual et al., Persistent cortical activity: mechanisms of generation and effects on neuronal excitability, Cerebral Cortex, vol.13, issue.11, pp.1219-1231, 2003.
URL : https://hal.archives-ouvertes.fr/hal-00018783

M. K. Mccoy and M. G. Tansey, TNF signaling inhibition in the CNS: implications for normal brain function and neurodegenerative disease, Journal of Neuroinflammation, vol.5, issue.1, p.45, 2008.

N. Medvedev, V. Popov, C. Henneberger, I. Kraev, D. A. Rusakov et al., Glia selectively approach synapses on thin dendritic spines, Phil. Trans. R. Soc. B, vol.369, p.20140047, 1654.

W. Men, D. Falk, T. Sun, W. Chen, J. Li et al., The corpus callosum of Albert Einsteins brain: another clue to his high intelligence, Brain, vol.137, issue.4, pp.268-268, 2014.

P. Mergenthaler, U. Lindauer, G. A. Dienel, and A. Meisel, Sugar for the brain: the role of glucose in physiological and pathological brain function, Trends in Neurosciences, vol.36, issue.10, pp.587-597, 2013.

P. Mesejo, O. Ibánez, E. Fernández-blanco, F. Cedrón, A. Pazos et al., Artificial neuron-glia networks learning approach based on cooperative coevolution, International Journal of Neural Systems, vol.25, issue.04, p.1550012, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01221226

R. Min and T. Nevian, Astrocyte signaling controls spike timing-dependent depression at neocortical synapses, Nat. Neurosci, vol.15, issue.5, pp.746-753, 2012.

A. V. Molofsky, K. W. Kelley, H. Tsai, S. A. Redmond, S. M. Chang et al., Astrocyte-encoded positional cues maintain sensorimotor circuit integrity, Nature, vol.509, issue.7499, p.189, 2014.

T. D. Montero and J. A. Orellana, Hemichannels: new pathways for gliotransmitter release, Neuroscience, vol.286, pp.45-59, 2015.

J. W. Moore, R. W. Joyner, M. H. Brill, S. D. Waxman, N. et al., Simulations of conduction in uniform myelinated fibers. Relative sensitivity to changes in nodal and internodal parameters, Biophysical Journal, vol.21, issue.2, pp.147-160, 1978.

R. Moreno-bote, J. Beck, I. Kanitscheider, X. Pitkow, P. Latham et al., Information-limiting correlations, Nature Neuroscience, vol.17, issue.10, p.1410, 2014.

P. Morquette, D. Verdier, A. Kadala, J. Féthì-ere, A. G. Philippe et al., An astrocyte-dependent mechanism for neuronal rhythmogenesis, Nature Neuroscience, vol.18, issue.6, p.844, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01837612

B. Mota and S. Herculano-houzel, All brains are made of this: a fundamental building block of brain matter with matching neuronal and glial masses, Frontiers in Neuroanatomy, vol.8, p.127, 2014.

J. Mothet, A. T. Parent, H. Wolosker, R. O. Brady, D. J. Linden et al., D-serine is an endogenous ligand for the glycine site of the N-methyl-D-aspartate receptor, Proceedings of the National Academy of Sciences, vol.97, issue.9, pp.4926-4931, 2000.

T. Müller, T. Möller, J. Neuhaus, and H. Kettenmann, Electrical coupling among Bergmann glial cells and its modulation by glutamate receptor activation, Glia, vol.17, pp.274-284, 1996.

S. Mulligan and B. Macvicar, Calcium transients in astrocyte endfeet cause cerebrovascular constrictions, Nature, vol.431, issue.7005, pp.195-199, 2004.

K. K. Murai, L. N. Nguyen, F. Irie, Y. Yamaguchi, P. et al., Control of hippocampal dendritic spine morphology through ephrin-A3/EphA4 signaling, Nature Neuroscience, vol.6, issue.2, p.153, 2003.

E. A. Nagelhus, T. M. Mathiisen, and O. P. Ottersen, Aquaporin-4 in the central nervous system: cellular and subcellular distribution and coexpression with KIR4.1. Neuroscience, vol.129, pp.905-913, 2004.

M. Navarrete and A. Araque, Endocannabinoids mediate neuron-astrocyte communication, Neuron, vol.57, issue.6, pp.883-893, 2008.
DOI : 10.1016/j.neuron.2008.01.029

URL : https://doi.org/10.1016/j.neuron.2008.01.029

M. Navarrete, A. Díez, A. , and A. , Astrocytes in endocannabinoid signalling, Philosophical Transactions of the Royal Society B: Biological Sciences, vol.369, p.20130599, 1654.
DOI : 10.1098/rstb.2013.0599

URL : http://rstb.royalsocietypublishing.org/content/369/1654/20130599.full.pdf

M. Navarrete, G. Perea, D. De-sevilla, M. Gómez-gonzalo, A. Núñez et al., Astrocytes mediate in vivo cholinergic-induced synaptic plasticity, PLoS Biol, vol.10, issue.2, p.1001259, 2012.
DOI : 10.1371/journal.pbio.1001259

URL : https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.1001259&type=printable

K. Nave, Myelination and support of axonal integrity by glia, Nature, vol.468, issue.7321, p.244, 2010.
DOI : 10.1038/nature09614

M. Nedergaard, Direct signaling from astrocytes to neurons in cultures of mammalian brain cells, Science, vol.263, issue.5154, p.1768, 1994.

M. Nedergaard, B. R. Ransom, and S. A. Goldman, New roles for astrocytes: redefining the functional architecture of the brain, Trends Neurosci, vol.26, issue.10, pp.523-530, 2003.

T. Nevian and B. Sakmann, Spine Ca 2+ signaling in spike-timing-dependent plasticity, Journal of Neuroscience, vol.26, issue.43, pp.11001-11013, 2006.
DOI : 10.1523/jneurosci.1749-06.2006

URL : http://www.jneurosci.org/content/26/43/11001.full.pdf

E. Newman, Calcium increases in retinal glial cells evoked by light-induced neuronal activity, J. Neurosci, vol.25, issue.23, pp.5502-5510, 2005.
DOI : 10.1523/jneurosci.1354-05.2005

URL : http://www.jneurosci.org/content/25/23/5502.full.pdf

E. A. Newman, Propagation of intercellular calcium waves in retinal astrocytes and Müller cells, J. Neurosci, vol.21, pp.2215-2223, 2001.

E. A. Newman and K. R. Zahs, Calcium waves in retinal glial cells, Science, vol.275, pp.844-847, 1997.
DOI : 10.1126/science.275.5301.844

URL : http://europepmc.org/articles/pmc2410141?pdf=render

L. A. Newman, D. L. Korol, and P. E. Gold, Lactate produced by glycogenolysis in astrocytes regulates memory processing, PloS One, vol.6, issue.12, p.28427, 2011.
DOI : 10.1371/journal.pone.0028427

URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0028427&type=printable

R. A. Nicoll and D. Schmitz, Synaptic plasticity at hippocampal mossy fibre synapses, Nature Reviews Neuroscience, vol.6, issue.11, p.863, 2005.
DOI : 10.1038/nrn1786

H. Nie, H. Zhang, and H. Weng, Bidirectional neuron-glia interactions triggered by deficiency of glutamate uptake at spinal sensory synapses, J. Neurophysiol, vol.104, issue.2, pp.713-725, 2010.
DOI : 10.1152/jn.00282.2010

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2934930/pdf

G. Nikola, V. Andon, and O. Kaynak, Sliding mode algorithm for online learning in analog multilayer feedforward neural networks, Artificial Neural Networks and Neural Information Processing-ICANN/ICONIP 2003, pp.1064-1072, 2003.

A. Nimmerjahn, F. Kirchhoff, and F. Helmchen, Resting microglial cells are highly dynamic surveillants of brain parenchyma in vivo, Science, vol.308, issue.5726, pp.1314-1318, 2005.

A. Nimmerjahn, F. Kirchhoff, J. N. Kerr, and F. Helmchen, Sulforhodamine 101 as a specific marker of astroglia in the neocortex in vivo, Nat. Methods, vol.1, pp.31-37, 2004.

Y. Nir, R. J. Staba, T. Andrillon, V. V. Vyazovskiy, C. Cirelli et al., Regional slow waves and spindles in human sleep, Neuron, vol.70, issue.1, pp.153-169, 2011.
DOI : 10.1016/j.neuron.2011.02.043

URL : https://doi.org/10.1016/j.neuron.2011.02.043

N. A. Oberheim, T. Takano, X. Han, W. He, J. H. Lin et al., Uniquely hominid features of adult human astrocytes, J. Neurosci, vol.29, issue.10, pp.3276-3287, 2009.
DOI : 10.1523/jneurosci.4707-08.2009

URL : http://www.jneurosci.org/content/29/10/3276.full.pdf

D. H. O'connor, G. M. Wittenberg, W. , S. S. , and .. , Graded bidirectional synaptic plasticity is composed of switch-like unitary events, Proceedings of the National Academy of Sciences, vol.102, issue.27, pp.9679-9684, 2005.

K. Ohki, S. Chung, Y. H. Ch'ng, P. Kara, R. et al., Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex, Nature, vol.433, issue.7026, p.597, 2005.
DOI : 10.1038/nature03274

M. Olah, K. Biber, J. Vinet, and H. W. Boddeke, Microglia phenotype diversity, CNS & Neurological Disorders-Drug Targets, vol.10, issue.1, pp.108-118, 2011.

S. H. Oliet and J. Mothet, Regulation of ¡ i¿N¡/i¿-methyl-D-aspartate receptors by astrocytic D-serine, Neuroscience, vol.158, issue.1, pp.275-283, 2009.

S. H. Oliet, R. Piet, and D. A. Poulain, Control of glutamate clearance and synaptic efficacy by glial coverage of neurons, Science, vol.292, pp.923-926, 2001.
URL : https://hal.archives-ouvertes.fr/inserm-00000059

J. F. Oliveira, V. M. Sardinha, S. Guerra-gomes, A. Araque, and N. Sousa, Do stars govern our actions? Astrocyte involvement in rodent behavior, Trends in neurosciences, vol.38, issue.9, pp.535-549, 2015.

A. Omrani, M. Melone, M. Bellesi, V. Safiulina, T. Aida et al., Up-regulation of GLT-1 severely impairs LTD at mossy fibre-CA3 synapses, The Journal of Physiology, vol.587, issue.19, pp.4575-4588, 2009.

L. A. O'neill and C. Kaltschmidt, NF-?B: a crucial transcription factor for glial and neuronal cell function, Trends in Neurosciences, vol.20, issue.6, pp.252-258, 1997.

R. K. Orkand, J. G. Nicholls, and S. W. Kuffler, Effect of nerve impulses on the membrane potential of glial cells in the central nervous system of amphibia, Journal of Neurophysiology, vol.29, issue.4, pp.788-806, 1966.

I. Østby, L. Øyehaug, G. T. Einevoll, E. A. Nagelhus, E. Plahte et al., Astrocytic mechanisms explaining neural-activityinduced shrinkage of extraneuronal space, PLoS Computational Biology, vol.5, issue.1, p.1000272, 2009.

Y. Otsu, K. Couchman, D. G. Lyons, M. Collot, A. Agarwal et al., Calcium dynamics in astrocyte processes during neurovascular coupling, Nature Neuroscience, vol.18, issue.2, p.210, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01362700

L. Øyehaug, I. Østby, C. M. Lloyd, S. W. Omholt, and G. T. Einevoll, Dependence of spontaneous neuronal firing and depolarisation block on astroglial membrane transport mechanisms, Journal of Computational Neuroscience, vol.32, issue.1, pp.147-165, 2012.

O. Palygin, U. Lalo, A. Verkhratsky, P. , and Y. , Ionotropic NMDA and P2X 1/5 receptors mediate synaptically induced Ca 2+ signalling in cortical astrocytes, Cell calcium, vol.48, issue.4, pp.225-231, 2010.

A. Panatier, D. T. Theodosis, J. P. Mothet, B. Touquet, L. Pollegioni et al., Glia-derived d-serine controls nmda receptor activity and synaptic memory, Cell, vol.125, pp.775-784, 2006.
URL : https://hal.archives-ouvertes.fr/inserm-00078312

U. Pannasch, D. Freche, G. Dallérac, G. Ghézali, C. Escartin et al., Connexin 30 sets synaptic strength by controlling astroglial synapse invasion, Nature neuroscience, vol.17, issue.4, p.549, 2014.

R. C. Paolicelli, G. Bolasco, F. Pagani, L. Maggi, M. Scianni et al., Synaptic pruning by microglia is necessary for normal brain development, Science, vol.333, issue.6048, pp.1456-1458, 2011.

T. Papouin, L. Ladépêche, J. Ruel, S. Sacchi, M. Labasque et al., Synaptic and extrasynaptic NMDA receptors are gated by different endogenous coagonists, Cell, vol.150, issue.3, pp.633-646, 2012.

V. Parpura, T. A. Basarsky, F. Liu, K. Jeftinija, S. Jeftinija et al., , 1994.

, Glutamate-mediated astrocyte-neuron signalling, Nature, vol.369, pp.744-747

V. Parpura and P. G. Haydon, Physiological astrocytic calcium levels stimulate glutamate release to modulate adjacent neurons, Proc. Natl. Acad. Sci. USA, vol.97, pp.8629-8634, 2000.

B. Parys, A. Côté, V. Gallo, P. De-koninck, and A. Sík, Intercellular calcium signaling between astrocytes and oligodendrocytes via gap junctions in culture, Neuroscience, vol.167, issue.4, pp.1032-1043, 2010.

O. Pascual, S. Ben-achour, P. Rostaing, A. Triller, and A. Bessis, Microglia activation triggers astrocyte-mediated modulation of excitatory neurotransmission, Proceedings of the National Academy of Sciences, pp.1-9, 2011.

O. Pascual, K. B. Casper, C. Kubera, J. Zhang, R. Revilla-sanchez et al., Astrocytic purinergic signaling coordinates synaptic networks, Science, vol.310, pp.113-116, 2005.

E. B. Pasquale, Eph-ephrin bidirectional signaling in physiology and disease, Cell, vol.133, issue.1, pp.38-52, 2008.

L. Pasti, A. Volterra, T. Pozzan, C. , and G. , Intracellular calcium oscillations in astrocytes: a highly plastic, bidirectional form of communication between neurons and astrocytes in situ, J. Neurosci, vol.17, issue.20, pp.7817-7830, 1997.

L. Pasti, M. Zonta, T. Pozzan, S. Vicini, C. et al., Cytosolic calcium oscillations in astrocytes may regulate exocytotic release of glutamate, J. Neurosci, vol.21, issue.2, pp.477-484, 2001.

M. Paukert, A. Agarwal, J. Cha, V. A. Doze, J. U. Kang et al., Norepinephrine controls astroglial responsiveness to local circuit activity, Neuron, vol.82, issue.6, pp.1263-1270, 2014.

L. Pellerin and P. J. Magistretti, Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization, Proceedings of the National Academy of Sciences, vol.91, issue.22, pp.10625-10629, 1994.

L. Pellerin and P. J. Magistretti, Sweet sixteen for ANLS, Journal of Cerebral Blood Flow & Metabolism, vol.32, issue.7, pp.1152-1166, 2012.

D. P. Pelvig, H. Pakkenberg, A. K. Stark, P. , and B. , Neocortical glial cell numbers in human brains, Neurobiology of Aging, vol.29, issue.11, pp.1754-1762, 2008.

W. Penfield, Cytology and Cellular Pathology of the Nervous System, vol.2, pp.421-479, 1932.

G. Perea and A. Araque, Properties of synaptically evoked astrocyte calcium signal reveal synaptic information processing by astrocyte, J. Neurosci, vol.25, issue.9, pp.2192-2203, 2005.

G. Perea and A. Araque, Astrocytes potentiate transmitter release at single hippocampal synapses, Science, vol.317, pp.1083-1086, 2007.

G. Perea, A. Yang, E. S. Boyden, and M. Sur, Optogenetic astrocyte activation modulates response selectivity of visual cortex neurons in vivo, Nature Communications, vol.5, p.4262, 2014.

A. Perez-alvarez, M. Navarrete, A. Covelo, E. D. Martin, A. et al., Structural and functional plasticity of astrocyte processes and dendritic spine interactions, The Journal of Neuroscience, vol.34, issue.38, pp.12738-12744, 2014.

D. H. Perkel and T. H. Bullock, Neural coding: a report based on an nrp work session, Neurosci. Res. Program Bull, vol.6, p.219349, 1968.

V. Pernice, B. Staude, S. Cardanobile, and S. Rotter, How structure determines correlations in neuronal networks, PLoS Computational Biology, vol.7, issue.5, p.1002059, 2011.

J. Petit, J. Gyger, S. Burlet-godinot, H. Fiumelli, J. Martin et al., Genes involved in the astrocyte-neuron lactate shuttle (ANLS) are specifically regulated in cortical astrocytes following sleep deprivation in mice, Sleep, vol.36, issue.10, pp.1445-1458, 2013.

J. Petit and P. J. Magistretti, Regulation of neuron-astrocyte metabolic coupling across the sleep-wake cycle, Neuroscience, vol.323, pp.135-156, 2016.

R. T. Philips, M. Sur, and V. S. Chakravarthy, The influence of astrocytes on the width of orientation hypercolumns in visual cortex: A computational perspective, PLoS Computational Biology, vol.13, issue.10, p.1005785, 2017.

R. Piet, D. A. Poulain, and S. H. Oliet, Contribution of astrocytes to synaptic transmission in the rat supraoptic nucleus, Neurochemistry International, vol.45, issue.2-3, pp.251-257, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00000070

R. Piet, L. Vargová, E. Syková, D. Poulain, and S. Oliet, Physiological contribution of the astrocytic environment of neurons to intersynaptic crosstalk, Proc. Natl. Acad. Sci. USA, vol.101, issue.7, pp.2151-2155, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00000063

P. S. Pinheiro and C. Mulle, Presynaptic glutamate receptors: physiological functions and mechanisms of action, Nature Reviews Neuroscience, vol.9, pp.423-436, 2008.

J. M. Pocock and H. Kettenmann, Neurotransmitter receptors on microglia, Trends in Neurosciences, vol.30, issue.10, pp.527-535, 2007.

J. T. Porter, B. Cauli, J. F. Staiger, B. Lambolez, J. Rossier et al., Properties of bipolar VIPergic interneurons and their excitation by pyramidal neurons in the rat neocortex, European Journal of Neuroscience, vol.10, issue.12, pp.3617-3628, 1998.

J. T. Porter and K. D. Mccarthy, Hippocampal astrocytes in situ respond to glutamate released from synaptic terminals, J. Neurosci, vol.16, issue.16, pp.5073-5081, 1996.

J. T. Porter and K. D. Mccarthy, Astrocytic neurotransmitter receptors ¡i¿in situ¡/i¿ and ¡i¿in vivo¡/i¿, Progress in Neurobiology, vol.51, issue.4, pp.439-455, 1997.

A. B. Porto-pazos, N. Veiguela, P. Mesejo, M. Navarrete, A. Alvarellos et al., Artificial astrocytes improve neural network performance, PloS one, vol.6, issue.4, p.19109, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01221307

K. E. Poskanzer and R. Yuste, Astrocytes regulate cortical state switching in vivo, Proceedings of the National Academy of Sciences, vol.113, issue.19, pp.2675-2684, 2016.

H. Pribiag and D. Stellwagen, TNF-? downregulates inhibitory neurotransmission through protein phosphatase 1-dependent trafficking of GABA A receptors, The Journal of Neuroscience, vol.33, issue.40, pp.15879-15893, 2013.

D. L. Price, J. W. Ludwig, H. Mi, T. L. Schwarz, and M. H. Ellisman, Distribution of rSlo Ca 2+-activated K + channels in rat astrocyte perivascular endfeet, Brain Research, vol.956, issue.2, pp.183-193, 2002.

V. Rajani, Y. Zhang, V. Jalubula, V. Rancic, S. Sheikhbahaei et al., Release of ATP by preBötzinger complex astrocytes contributes to the hypoxic ventilatory response via a Ca 2+-dependent P2Y 1 receptor mechanism, The Journal of physiology, vol.589, pp.4583-4600, 2017.

C. B. Ransom, B. R. Ransom, and H. Sontheimer, Activity-dependent extracellular K + accumulation in rat optic nerve: the role of glial and axonal Na + pumps, The Journal of physiology, vol.522, issue.3, pp.427-442, 2000.

A. Reichenbach, A. Derouiche, and F. Kirchhoff, Morphology and dynamics of perisynaptic glia, Brain Research Reviews, vol.63, issue.1, pp.11-25, 2010.

A. Reichenbach and S. R. Robinson, Phylogenetic constraints on retinal organisation and development, Progress in Retinal and Eye Research, vol.15, issue.1, pp.139-171, 1995.

A. G. Richardson, C. C. Mcintyre, and W. M. Grill, Modelling the effects of electric fields on nerve fibres: influence of the myelin sheath, Medical and Biological Engineering and Computing, vol.38, issue.4, pp.438-446, 2000.

M. Rigotti, O. Barak, M. R. Warden, X. Wang, N. D. Daw et al., The importance of mixed selectivity in complex cognitive tasks, Nature, vol.497, issue.7451, p.585, 2013.

M. T. Roberts, S. C. Seeman, and N. L. Golding, A mechanistic understanding of the role of feedforward inhibition in the mammalian sound localization circuitry, Neuron, vol.78, issue.5, pp.923-935, 2013.

C. R. Rose and J. Chatton, Astrocyte sodium signaling and neuro-metabolic coupling in the brain, Neuroscience, vol.323, pp.121-134, 2016.

D. L. Rothman, K. L. Behar, F. Hyder, and R. G. Shulman, vivo NMR studies of the glutamate neurotransmitter flux and neuroenergetics: implications for brain function, vol.65, pp.401-427, 2003.

J. D. Rothstein, M. Dykes-hoberg, C. A. Pardo, L. A. Bristol, L. Jin et al., Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate, Neuron, vol.16, issue.3, pp.675-686, 1996.

A. Roxin, N. Brunel, H. , and D. , Role of delays in shaping spatiotemporal dynamics of neuronal activity in large networks, Physical Review Letters, vol.94, issue.23, p.238103, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00173796

A. Roxin and E. Montbrió, How effective delays shape oscillatory dynamics in neuronal networks, Physica D: Nonlinear Phenomena, vol.240, issue.3, pp.323-345, 2011.

D. A. Rusakov, The role of perisynaptic glial sheaths in glutamate spillover and extracellular Ca 2+ depletion, Biophysical Journal, vol.81, issue.4, pp.1947-1959, 2001.

D. A. Rusakov, Disentangling calcium-driven astrocyte physiology, Nature Reviews Neuroscience, vol.16, pp.226-233, 2015.

W. A. Rushton, A theory of the effects of fibre size in medullated nerve, The Journal of Physiology, vol.115, issue.1, pp.101-122, 1951.

B. L. Sabatini and W. G. Regehr, Timing of synaptic transmission, Annual Review of Physiology, vol.61, issue.1, pp.521-542, 1999.

D. A. Sahlender, I. Savtchouk, and A. Volterra, What do we know about gliotransmitter release from astrocytes? Phil, Tran. R. Soc. B, vol.369, 2014.

M. Salami, C. Itami, T. Tsumoto, and F. Kimura, Change of conduction velocity by regional myelination yields constant latency irrespective of distance between thalamus and cortex, Proceedings of the National Academy of Sciences, vol.100, issue.10, pp.6174-6179, 2003.

M. V. Sanchez-vives and D. A. Mccormick, Cellular and network mechanisms of rhythmic recurrent activity in neocortex, Nature Neuroscience, vol.3, issue.10, p.1027, 2000.

M. Santello, P. Bezzi, and A. Volterra, TNF? controls glutamatergic gliotransmission in the hippocampal dentate gyrus, Neuron, vol.69, pp.988-1001, 2011.

M. Santello and A. Volterra, TNF? in synaptic function: switching gears, Trends in Neurosci, vol.35, issue.10, pp.638-647, 2012.

R. Sarpeshkar, Analog versus digital: extrapolating from electronics to neurobiology, Neural Computation, vol.10, issue.7, pp.1601-1638, 1998.

T. Sasaki, N. Matsuki, and Y. Ikegaya, Action-potential modulation during axonal conduction, Science, vol.331, issue.6017, pp.599-601, 2011.

C. Savin, J. Triesch, and M. Meyer-hermann, Epileptogenesis due to glia-mediated synaptic scaling, Journal of The Royal Society Interface, vol.6, issue.37, pp.655-668, 2009.

L. P. Savtchenko and D. A. Rusakov, Regulation of rhythm genesis by volume-limited, astroglia-like signals in neural networks, Phil. Trans. Royal Soc. B: Biological Sciences, vol.369, p.20130614, 1654.

I. Savtchouk and A. Volterra, Gliotransmission: Beyond black-and-white, Journal of Neuroscience, vol.38, issue.1, pp.14-25, 2018.

E. Scemes and C. Giaume, Astrocyte calcium waves: What they are and what they do, Glia, vol.54, pp.716-725, 2006.

D. P. Schafer, E. K. Lehrman, A. G. Kautzman, R. Koyama, A. R. Mardinly et al., Microglia sculpt postnatal neural circuits in an activity and complement-dependent manner, Neuron, vol.74, issue.4, pp.691-705, 2012.

C. G. Schipke, C. Boucsein, C. Ohlemeyer, F. Kirchhoff, and H. Kettenmann, Astrocyte Ca 2+ waves trigger responses in microglial cells in brain slices, The FASEB Journal, vol.16, issue.2, pp.255-257, 2002.

V. J. Schmithorst and M. Wilke, Differences in white matter architecture between musicians and non-musicians: a diffusion tensor imaging study, Neuroscience letters, vol.321, issue.12, pp.57-60, 2002.

L. Schmitt, R. Sims, N. Dale, H. , and P. , Wakefulness affects synaptic and network activity by increasing extracellular astrocyte-derived adenosine, J. Neurosci, vol.32, issue.13, pp.4417-4425, 2012.

J. Scholz, M. C. Klein, T. E. Behrens, and H. Johansen-berg, Training induces changes in white-matter architecture, Nature Neuroscience, vol.12, issue.11, p.1370, 2009.

J. Schummers, H. Yu, and M. Sur, Tuned responses of astrocytes and their influence on hemodynamic signals in the visual cortex, Sci. STKE, vol.320, issue.5883, p.1638, 2008.

S. Schuster, M. Marhl, and T. Höfer, Modelling of simple and complex calcium oscillations from single-cell responses to intercellular signalling, Eur. J. Biochem, vol.269, pp.1333-1355, 2002.

A. H. Seidl, E. W. Rubel, H. , and D. M. , Mechanisms for adjusting interaural time differences to achieve binaural coincidence detection, Journal of Neuroscience, vol.30, issue.1, pp.70-80, 2010.

G. Seifert and C. Steinhäuser, Heterogeneity and function of hippocampal macroglia, Cell and Tissue Research, pp.1-18, 2017.

H. S. Seung, D. D. Lee, B. Y. Reis, and D. W. Tank, The autapse: a simple illustration of short-term analog memory storage by tuned synaptic feedback, Journal of Computational Neuroscience, vol.9, issue.2, pp.171-185, 2000.

S. Sheikhbahaei, E. A. Turovsky, P. S. Hosford, A. Hadjihambi, S. M. Theparambil et al., , 2018.

, Astrocytes modulate brainstem respiratory rhythm-generating circuits and determine exercise capacity, Nature communications, vol.9, issue.1, p.370

M. W. Sherwood, M. Arizono, C. Hisatsune, H. Bannai, E. Ebisui et al., Astrocytic ip3rs: Contribution to ca2+ signalling and hippocampal ltp, Glia, vol.65, issue.3, pp.502-513, 2017.
DOI : 10.1002/glia.23107

E. Shigetomi, O. Jackson-weaver, R. T. Huckstepp, T. J. O'dell, and B. S. Khakh, TRPA1 channels are regulators of astrocyte basal calcium levels and long-term potentiation via constitutive D-serine release, The Journal of Neuroscience, vol.33, issue.24, pp.10143-10153, 2013.

E. Shigetomi, X. Tong, K. Kwan, D. Corey, and B. Khakh, TRPA1 channels regulate astrocyte resting calcium levels and inhibitory synapse efficacy via GAT-3, Nat. Neurosci, vol.15, issue.1, pp.70-80, 2012.

J. M. Siegel, Clues to the functions of mammalian sleep, Nature, vol.437, issue.7063, p.1264, 2005.

M. Sild and E. S. Ruthazer, Radial glia: progenitor, pathway, and partner, The Neuroscientist, vol.17, issue.3, pp.288-302, 2011.
DOI : 10.1177/1073858410385870

M. Simard and M. Nedergaard, The neurobiology of glia in the context of water and ion homeostasis, Neuroscience, vol.129, issue.4, pp.877-896, 2004.

I. A. Simpson, A. Carruthers, and S. J. Vannucci, Supply and demand in cerebral energy metabolism: the role of nutrient transporters, Journal of Cerebral Blood Flow & Metabolism, vol.27, issue.11, pp.1766-1791, 2007.

G. O. Sipe, R. L. Lowery, M. Tremblay, E. A. Kelly, C. E. Lamantia et al.,

A. K. , Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex, Nature Communications, vol.7, p.10905, 2016.

H. Sira-ramirez and E. Colina-morles, A sliding mode strategy for adaptive learning in adalines, IEEE Transactions on Circuits and Systems I: Fundamental Theory and Applications, vol.42, issue.12, pp.1001-1012, 1995.

A. Skupin, H. Kettenmann, U. Winkler, M. Wartenberg, H. Sauer et al., How does intracellular Ca 2+ oscillate: by chance or by clock?, Biophys. J, vol.94, pp.2404-2411, 2008.

E. Somersalo, Y. Cheng, C. , and D. , The metabolism of neurons and astrocytes through mathematical models, Annals of Biomedical Engineering, vol.40, issue.11, pp.2328-2344, 2012.

G. G. Somjen, Ion regulation in the brain: implications for pathophysiology, The Neuroscientist, vol.8, issue.3, pp.254-267, 2002.

G. G. Somjen, H. Kager, and W. J. Wadman, Computer simulations of neuron-glia interactions mediated by ion flux, Journal of Computational Neuroscience, vol.25, issue.2, pp.349-365, 2008.

O. Sorg and P. J. Magistretti, Characterization of the glycogenolysis elicited by vasoactive intestinal peptide, noradrenaline and adenosine in primary cultures of mouse cerebral cortical astrocytes, Brain Research, vol.563, issue.1-2, pp.227-233, 1991.

O. Sorg and P. J. Magistretti, Vasoactive intestinal peptide and noradrenaline exert long-term control on glycogen levels in astrocytes: blockade by protein synthesis inhibition, Journal of Neuroscience, vol.12, issue.12, pp.4923-4931, 1992.

R. Srinivasan, B. S. Huang, S. Venugopal, A. D. Johnston, H. Chai et al., Ca 2+ signaling in astrocytes from Ip3r2 ?/? mice in brain sslice and during startle responses in vivo, Nature Neuroscience, vol.18, pp.708-717, 2015.

R. Stassart, S. Goebbels, and K. Nave, Neuroglia, chapter Factors controlling myelin formation, pp.555-572, 2013.

J. Stehberg, R. Moraga-amaro, C. Salazar, A. Becerra, C. Echeverría et al., Release of gliotransmitters through astroglial connexin 43 hemichannels is necessary for fear memory consolidation in the basolateral amygdala, The FASEB Journal, vol.26, issue.9, pp.3649-3657, 2012.

C. Steinhaüser, T. Berger, M. Frotscher, and H. Kettenmann, Heterogeneity in the membrane current pattern of identified glial cells in the hippocampal slice, European Journal of Neuroscience, vol.4, issue.6, pp.472-484, 1992.

C. C. Steinmetz and G. G. Turrigiano, Tumor necrosis factor-? signaling maintains the ability of cortical synapses to express synaptic scaling, Journal of Neuroscience, vol.30, issue.44, pp.14685-14690, 2010.

D. Stellwagen, E. C. Beattie, J. Y. Seo, and R. C. Malenka, Differential regulation of AMPA receptor and GABA receptor trafficking by tumor necrosis factor-?, J. Neurosci, vol.25, issue.12, pp.3219-3228, 2005.

D. Stellwagen and R. C. Malenka, Synaptic scaling mediated by glial TNF-?, Nature, vol.440, issue.7087, pp.1054-1059, 2006.

B. Stevens, N. J. Allen, L. E. Vazquez, G. R. Howell, K. S. Christopherson et al., The classical complement cascade mediates CNS synapse elimination, Cell, vol.131, issue.6, pp.1164-1178, 2007.

J. R. Stevens, J. S. Law, J. Antolík, and J. A. Bednar, Mechanisms for stable, robust, and adaptive development of orientation maps in the primary visual cortex, Journal of Neuroscience, vol.33, issue.40, pp.15747-15766, 2013.

J. L. Stobart, K. D. Ferrari, M. J. Barrett, C. Glück, M. J. Stobart et al., Cortical circuit activity evokes rapid astrocyte calcium signals on a similar timescale to neurons. Neuron, vol.98, pp.726-735, 2018.

C. E. Stout, J. L. Costantin, C. C. Naus, C. , and A. C. , Intercellular calcium signaling in astocytes via ATP release through connexin hemichannels, J. Biol. Chem, vol.277, issue.12, pp.10482-10488, 2002.

S. Strohschein, K. Hüttmann, S. Gabriel, D. K. Binder, U. Heinemann et al., Impact of aquaporin-4 channels on K + buffering and gap junction coupling in the hippocampus, Glia, vol.59, issue.6, pp.973-980, 2011.

S. O. Suadicani, C. F. Brosnan, and E. Scemes, P2X 7 receptors mediate ATP release and amplification of astrocytic intercellular Ca 2+ signaling, Journal of Neuroscience, vol.26, issue.5, pp.1378-1385, 2006.

T. C. Südhof, The synaptic vesicle cycle, Annu. Rev. Neurosci, vol.27, pp.509-547, 2004.

I. Sugihara, E. J. Lang, and R. Llinás, Uniform olivocerebellar conduction time underlies purkinje cell complex spike synchronicity in the rat cerebellum, The Journal of Physiology, vol.470, issue.1, pp.243-271, 1993.

A. Suzuki, S. A. Stern, B. Huntely, G. Wlaker, R. H. Magistretti et al., Astrocyte-neuron lactate transport is required for long-term memory formation, Cell, vol.144, pp.810-823, 2011.

F. Ullén, Is activity regulation of late myelination a plastic mechanism in the human nervous system?, Neuron Glia Biology, vol.5, issue.1-2, pp.29-34, 2009.

S. N. Vaishnavi, A. G. Vlassenko, M. M. Rundle, A. Z. Snyder, M. A. Mintun et al., Regional aerobic glycolysis in the human brain, Proceedings of the National Academy of Sciences, vol.107, issue.41, pp.17757-17762, 2010.

S. Valtcheva and L. Venance, Astrocytes gate Hebbian synaptic plasticity in the striatum, Nature Communications, vol.7, p.13845, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01429821

R. Ventura and K. M. Harris, Three-dimensional relationships between hippocampal synapses and astrocytes, J. Neurosci, vol.19, issue.16, pp.6897-6906, 1999.

D. Verbich, G. A. Prenosil, P. K. Chang, K. K. Murai, and R. A. Mckinney, Glial glutamate transport modulates dendritic spine head protrusions in the hippocampus, Glia, vol.60, issue.7, pp.1067-1077, 2012.

C. Verderio and M. Matteoli, ATP mediates calcium signaling between astrocytes and microglial cells: modulation by IFN-?, The Journal of Immunology, vol.166, issue.10, pp.6383-6391, 2001.

A. Verkhratsky and H. Kettenmann, Calcium signaling in glial cells, Trends Neurosci, vol.19, pp.346-352, 1996.

A. Verkhratsky and M. Nedergaard, The homeostatic astroglia emerges from evolutionary specialization of neural cells, Phil. Trans. R. Soc. B, vol.371, p.20150428, 1700.

J. D. Violin, L. M. Dipilato, N. Yildirim, T. C. Elston, J. Zhang et al., ?2-adrenergic receptor signaling and desensitization elucidated by quantitative modeling of real time cAMP dynamics, Journal of Biological Chemistry, vol.283, issue.5, pp.2949-2961, 2008.

V. Volman, M. Bazhenov, and T. J. Sejnowski, Divide and conquer: functional segregation of synaptic inputs by astrocytic microdomains could alleviate paroxysmal activity following brain trauma, PLoS Computational Biology, vol.9, issue.1, p.1002856, 2013.

V. Volman, E. Ben-jacob, and H. Levine, The astrocyte as a gatekeeper of synaptic information transfer, Neural Computation, vol.19, pp.303-326, 2007.

A. Volterra, N. Liaudet, and I. Savtchouk, , 2014.

, Astrocyte Ca 2+ signalling: an unexpected complexity, Nature Reviews Neuroscience, vol.15, pp.327-334

V. V. Vyazovskiy, C. Cirelli, M. Pfister-genskow, U. Faraguna, and G. Tononi, Molecular and electrophysiological evidence for net synaptic potentiation in wake and depression in sleep, Nature Neuroscience, vol.11, issue.2, p.200, 2008.

V. V. Vyazovskiy and K. D. Harris, Sleep and the single neuron: the role of global slow oscillations in individual cell rest, Nature Reviews Neuroscience, vol.14, issue.6, p.443, 2013.

V. V. Vyazovskiy, U. Olcese, E. C. Hanlon, Y. Nir, C. Cirelli et al., Local sleep in awake rats, Nature, vol.472, issue.7344, p.443, 2011.

T. V. Waehneldt, J. Matthieu, J. , and G. , Appearance of myelin proteins during vertebrate evolution, Neurochemistry International, vol.9, issue.4, pp.463-474, 1986.

H. Wake, A. J. Moorhouse, S. Jinno, S. Kohsaka, and J. Nabekura, Resting microglia directly monitor the functional state of synapses in vivo and determine the fate of ischemic terminals, Journal of Neuroscience, vol.29, issue.13, pp.3974-3980, 2009.

H. Wake, A. J. Moorhouse, A. Miyamoto, and J. Nabekura, Microglia: actively surveying and shaping neuronal circuit structure and function, Trends in Neurosciences, vol.36, issue.4, pp.209-217, 2013.

W. Walz, Role of astrocytes in the clearance of excess extracellular potassium, Neurochemistry international, vol.36, issue.4-5, pp.291-300, 2000.

F. Wang, Q. Xu, W. Wang, T. Takano, N. et al., Bergmann glia modulate cerebellar purkinje cell bistability via Ca 2+-dependent K + uptake, Proc. Natl. Acad. Sci. USA, vol.109, issue.20, pp.7911-7916, 2012.

X. Wang, N. Lou, Q. Xu, G. Tian, W. G. Peng et al., Astrocytic Ca 2+ signaling evoked by sensory stimulation in vivo, Nat. Neurosci, vol.9, issue.6, pp.816-823, 2006.

S. G. Waxman, Determinants of conduction velocity in myelinated nerve fibers, Muscle & Nerve, vol.3, issue.2, pp.141-150, 1980.

S. G. Waxman and M. V. Bennett, Relative conduction velocities of small myelinated and non-myelinated fibres in the central nervous system, Nature New Biology, vol.238, issue.85, p.217, 1972.

D. B. Wheeler, A. Randall, and R. W. Tsien, Changes in action potential duration alter reliance of excitatory synaptic transmission on multiple types of ca2+ channels in rat hippocampus, Journal of Neuroscience, vol.16, issue.7, pp.2226-2237, 1996.

T. N. Wiesel, Postnatal development of the visual cortex and the influence of environment, Nature, vol.299, issue.5884, p.583, 1982.

I. Winship, N. Plaa, M. , and T. , Rapid astrocyte calcium signals correlate with neuronal activity and onset of the hemodynamic response in vivo, J. Neurosci, vol.27, issue.23, pp.6268-6272, 2007.

M. Witcher, S. Kirov, H. , and K. , Plasticity of perisynaptic astroglia during synaptogenesis in the mature rat hippocampus, Glia, vol.55, issue.1, pp.13-23, 2007.

S. F. Witelson, D. L. Kigar, H. , and T. , The exceptional brain of Albert Einstein, The Lancet, vol.353, issue.9170, pp.2149-2153, 1999.

D. H. Woo, K. Han, J. W. Shim, B. Yoon, E. Kim et al., TREK-1 and Best1 channels mediate fast and slow glutamate release in astrocytes upon GPCR activation, Cell, vol.151, issue.1, pp.25-40, 2012.

X. Wu, L. Pan, Y. Liu, P. Jiang, I. Lee et al., , 2013.

, Cell-cell communication induces random spikes of spontaneous calcium oscillations in multiBV-2 microglial cells, Biochemical and Biophysical Research Communications, vol.431, issue.4, pp.664-669

Y. Wu, L. Dissing-olesen, B. A. Macvicar, and B. Stevens, Microglia: dynamic mediators of synapse development and plasticity, Trends in Immunology, vol.36, issue.10, pp.605-613, 2015.

J. Xiang, S. R. Ennis, G. E. Abdelkarim, M. Fujisawa, N. Kawai et al., Glutamine transport at the blood-brain and blood-cerebrospinal fluid barriers, Neurochemistry International, vol.43, issue.4-5, pp.279-288, 2003.

L. Xie, H. Kang, Q. Xu, M. J. Chen, Y. Liao et al., Sleep drives metabolite clearance from the adult brain. science, vol.342, pp.373-377, 2013.

Y. Yamazaki, Y. Hozumi, K. Kaneko, T. Sugihara, S. Fujii et al., Modulatory effects of oligodendrocytes on the conduction velocity of action potentials along axons in the alveus of the rat hippocampal CA1 region, Neuron Glia Biology, vol.3, issue.4, pp.325-334, 2007.

L. Yang, Y. Qi, Y. , and Y. , Astrocytes control food intake by inhibiting AGRP neuron activity via adenosine a1 receptors, Cell Reports, vol.11, issue.5, pp.798-807, 2015.

S. Yang, H. Qiao, L. Wen, W. Zhou, and Y. Zhang, D-serine enhances impaired longterm potentiation in CA1 subfield of hippocampal slices from aged senescence-accelerated mouse prone/8, Neuroscience Letters, vol.379, issue.1, pp.7-12, 2005.

Y. Yang, W. Ge, Y. Chen, Z. Zhang, W. Shen et al., Contribution of astrocytes to hippocampal long-term potentiation through release of d-serine, Proc. Natl. Acad. Sci. USA, vol.100, issue.25, pp.15194-15199, 2003.

W. Ying, NAD + /NADH and NADP + /NADPH in cellular functions and cell death: regulation and biological consequences, Antioxidants & Redox Signaling, vol.10, issue.2, pp.179-206, 2008.

K. M. Young, K. Psachoulia, R. B. Tripathi, S. Dunn, L. Cossell et al., Oligodendrocyte dynamics in the healthy adult CNS: evidence for myelin remodeling, Neuron, vol.77, issue.5, pp.873-885, 2013.
DOI : 10.1016/j.neuron.2013.01.006

URL : https://doi.org/10.1016/j.neuron.2013.01.006

X. Yu, M. Zhihong, and S. M. Rahman, Adaptive sliding mode approach for learning in a feedforward neural network, Neural Computing & Applications, vol.7, issue.4, pp.289-294, 1998.

B. Zalc and D. R. Colman, Origins of vertebrate success, Science, vol.288, issue.5464, pp.271-271, 2000.
DOI : 10.1126/science.288.5464.271c

B. Zalc, D. Goujet, C. , and D. , The origin of the myelination program in vertebrates, Current Biology, vol.18, issue.12, pp.511-512, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01936252

F. Zenke, W. Gerstner, and S. Ganguli, The temporal paradox of Hebbian learning and homeostatic plasticity, Current Opinion in Neurobiology, vol.43, pp.166-176, 2017.

Y. Zhan, R. C. Paolicelli, F. Sforazzini, L. Weinhard, G. Bolasco et al., Deficient neuronmicroglia signaling results in impaired functional brain connectivity and social behavior, Nature Neuroscience, vol.17, issue.3, p.400, 2014.
DOI : 10.1038/nn.3641

Y. Zhang, K. Chen, S. A. Sloan, M. L. Bennett, A. R. Scholze et al., An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex, Journal of Neuroscience, vol.34, issue.36, pp.11929-11947, 2014.

Z. Zhang, N. Gong, W. Wang, L. Xu, and T. Xu, Bell-shaped D-serine actions on hippocampal long-term depression and spatial memory retrieval, Cerebral Cortex, vol.18, issue.10, pp.2391-2401, 2008.
DOI : 10.1093/cercor/bhn008

URL : https://academic.oup.com/cercor/article-pdf/18/10/2391/1095688/bhn008.pdf

E. Zohary, M. N. Shadlen, and W. T. Newsome, Correlated neuronal discharge rate and its implications for psychophysical performance, Nature, vol.370, issue.6485, p.140, 1994.
DOI : 10.1038/370140a0

M. Zonta, M. C. Angulo, S. Gobbo, B. Rosengarten, K. A. Hossmann et al., Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation, Nat. Neurosci, vol.6, pp.43-83, 2003.

R. Zorec, A. Araque, G. Carmignoto, P. Haydon, A. Verkhratsky et al., , 2012.

, Astroglial excitability and gliotransmission: An appraisal of Ca 2+ as a signaling route, ASN Neuro, vol.4, issue.2, p.80

R. S. Zucker and W. G. Regehr, Short-term synaptic plasticity, Annu. Rev. Physiol, vol.64, pp.355-405, 2002.