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hal-00542528, version 1

Adipocyte turnover: relevance to human adipose tissue morphology.

Erik Arner 1, Pål O Westermark 2, Kirsty L Spalding 1, Tom Britton 3, Mikael Rydén 4, Jonas Frisén 5, Samuel Bernard 67, Peter Arner 4

Diabetes 59, 1 (2010) 105-9

Abstract: OBJECTIVE: Adipose tissue may contain few large adipocytes (hypertrophy) or many small adipocytes (hyperplasia). We investigated factors of putative importance for adipose tissue morphology. RESEARCH DESIGN AND METHODS: Subcutaneous adipocyte size and total fat mass were compared in 764 subjects with BMI 18-60 kg/m(2). A morphology value was defined as the difference between the measured adipocyte volume and the expected volume given by a curved-line fit for a given body fat mass and was related to insulin values. In 35 subjects, in vivo adipocyte turnover was measured by exploiting incorporation of atmospheric (14)C into DNA. RESULTS: Occurrence of hyperplasia (negative morphology value) or hypertrophy (positive morphology value) was independent of sex and body weight but correlated with fasting plasma insulin levels and insulin sensitivity, independent of adipocyte volume (beta-coefficient = 0.3, P < 0.0001). Total adipocyte number and morphology were negatively related (r = -0.66); i.e., the total adipocyte number was greatest in pronounced hyperplasia and smallest in pronounced hypertrophy. The absolute number of new adipocytes generated each year was 70% lower (P < 0.001) in hypertrophy than in hyperplasia, and individual values for adipocyte generation and morphology were strongly related (r = 0.7, P < 0.001). The relative death rate (approximately 10% per year) or mean age of adipocytes (approximately 10 years) was not correlated with morphology. CONCLUSIONS: Adipose tissue morphology correlates with insulin measures and is linked to the total adipocyte number independently of sex and body fat level. Low generation rates of adipocytes associate with adipose tissue hypertrophy, whereas high generation rates associate with adipose hyperplasia.

  • 1:  Karolinska Institutet
  • Karolinska Institutet
  • 2:  Institute for Theoretical Biology (ITB)
  • University of Berlin
  • 3:  Department of Mathematics [Sweden] (KTH)
  • Stockholm University
  • 4:  Department of medicine [Stockholm]
  • Karolinska University Hospital – Karolinska Institutet
  • 5:  Department of Cell and Molecular Biology [Sweden] (DCMB)
  • Medical Nobel Institute
  • 6:  Institut Camille Jordan (ICJ)
  • CNRS : UMR5208 – Université Claude Bernard - Lyon I – Ecole Centrale de Lyon – Institut National des Sciences Appliquées (INSA) - Lyon
  • 7:  DRACULA (INRIA Grenoble Rhône-Alpes / Institut Camille Jordan)
  • INRIA – CNRS : UMR5534 – Université Claude Bernard - Lyon I : EA – Institut Camille Jordan
  • Domain : Mathematics/Dynamical Systems
    Life Sciences/Cellular Biology/Subcellular Processes
 
  • hal-00542528, version 1
  • oai:hal.archives-ouvertes.fr:hal-00542528
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  • Submitted on: Thursday, 2 December 2010 20:31:58
  • Updated on: Wednesday, 8 December 2010 13:45:01