Mitochondrial (dys)function in adipocyte (de)differentiation and systemic metabolic alterations

Am J Pathol. 2009 Sep;175(3):927-39. doi: 10.2353/ajpath.2009.081155. Epub 2009 Aug 21.

Abstract

In mammals, adipose tissue, composed of BAT and WAT, collaborates in energy partitioning and performs metabolic regulatory functions. It is the most flexible tissue in the body, because it is remodeled in size and shape by modifications in adipocyte cell size and/or number, depending on developmental status and energy fluxes. Although numerous reviews have focused on the differentiation program of both brown and white adipocytes as well as on the pathophysiological role of white adipose tissues, the importance of mitochondrial activity in the differentiation or the dedifferentiation programs of adipose cells and in systemic metabolic alterations has not been extensively reviewed previously. Here, we address the crucial role of mitochondrial functions during adipogenesis and in mature adipocytes and discuss the cellular responses of white adipocytes to mitochondrial activity impairment. In addition, we discuss the increase in scientific knowledge regarding mitochondrial functions in the last 10 years and the recent suspicion of mitochondrial dysfunction in several 21st century epidemics (ie, obesity and diabetes), as well as in lipodystrophy found in HIV-treated patients, which can contribute to the development of new therapeutic strategies targeting adipocyte mitochondria.

Publication types

  • Review

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / physiology*
  • Adipogenesis / physiology*
  • Animals
  • Cell Dedifferentiation / physiology
  • Cell Transdifferentiation / physiology
  • Glucose / metabolism
  • HIV Infections / physiopathology
  • HIV-Associated Lipodystrophy Syndrome / etiology
  • HIV-Associated Lipodystrophy Syndrome / metabolism
  • HIV-Associated Lipodystrophy Syndrome / therapy
  • Humans
  • Lipid Metabolism / physiology
  • Lipogenesis / physiology
  • Mice
  • Mitochondria / physiology*
  • Obesity / etiology
  • Obesity / metabolism
  • Obesity / physiopathology
  • Obesity / therapy

Substances

  • Glucose