Altered miRNA processing disrupts brown/white adipocyte determination and associates with lipodystrophy

J Clin Invest. 2014 Aug;124(8):3339-51. doi: 10.1172/JCI73468. Epub 2014 Jul 1.

Abstract

miRNAs are important regulators of biological processes in many tissues, including the differentiation and function of brown and white adipocytes. The endoribonuclease dicer is a major component of the miRNA-processing pathway, and in adipose tissue, levels of dicer have been shown to decrease with age, increase with caloric restriction, and influence stress resistance. Here, we demonstrated that mice with a fat-specific KO of dicer develop a form of lipodystrophy that is characterized by loss of intra-abdominal and subcutaneous white fat, severe insulin resistance, and enlargement and "whitening" of interscapular brown fat. Additionally, KO of dicer in cultured brown preadipocytes promoted a white adipocyte-like phenotype and reduced expression of several miRNAs. Brown preadipocyte whitening was partially reversed by expression of miR-365, a miRNA known to promote brown fat differentiation; however, introduction of other miRNAs, including miR-346 and miR-362, also contributed to reversal of the loss of the dicer phenotype. Interestingly, fat samples from patients with HIV-related lipodystrophy exhibited a substantial downregulation of dicer mRNA expression. Together, these findings indicate the importance of miRNA processing in white and brown adipose tissue determination and provide a potential link between this process and HIV-related lipodystrophy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / cytology
  • Adipocytes, Brown / metabolism*
  • Adipocytes, White / cytology*
  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cohort Studies
  • DEAD-box RNA Helicases / deficiency
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / metabolism
  • Disease Models, Animal
  • Down-Regulation
  • Energy Metabolism
  • Female
  • HIV-Associated Lipodystrophy Syndrome / genetics
  • HIV-Associated Lipodystrophy Syndrome / metabolism
  • HIV-Associated Lipodystrophy Syndrome / pathology
  • Humans
  • Insulin Resistance
  • Lipodystrophy / genetics*
  • Lipodystrophy / metabolism*
  • Lipodystrophy / pathology
  • Male
  • Mice
  • Mice, Knockout
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism*
  • RNA Processing, Post-Transcriptional
  • Ribonuclease III / deficiency
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism

Substances

  • MicroRNAs
  • DICER1 protein, human
  • Dicer1 protein, mouse
  • Ribonuclease III
  • DEAD-box RNA Helicases