Adipogenesis, lipogenesis and lipolysis is stimulated by mild but not severe hypoxia in 3T3-L1 cells

Biochem Biophys Res Commun. 2016 Sep 16;478(2):727-32. doi: 10.1016/j.bbrc.2016.08.015. Epub 2016 Aug 4.

Abstract

In-vitro investigation of the effects of hypoxia is limited by physical laws of gas diffusion and cellular O2 consumption, making prolonged exposures to stable O2 concentrations impossible. Using a gas-permeable cultureware, chronic effects of mild and severe hypoxia on triglyceride accumulation, lipid droplet size distribution, spontaneous lipolysis and gene expression of adipocyte-specific markers were assessed. 3T3-L1 cells were differentiated under 20%, 4% or 1% O2 using a gas-permeable cultureware. Triglyceride accumulation, expression of genes characteristic for advanced adipocyte differentiation and involvement of key lipogenesis enzymes were assessed after exposures. Lipogenesis increased by 375% under mild hypoxia, but dropped by 43% in severe hypoxia. Mild, but not severe, hypoxia increased formation of large lipid droplets 6.4 fold and strongly induced gene expression of adipocyte-specific markers. Spontaneous lipolysis increased by 488% in mild, but only by 135% in severe hypoxia. Inhibition of ATP-dependent citrate lyase suppressed hypoxia-induced lipogenesis by 81% and 85%. Activation of HIF inhibited lipogenesis by 59%. Mild, but not severe, hypoxia stimulates lipolysis and promotes adipocyte differentiation, probably through excess of acetyl-CoA originating from tricarboxylic acid cycle independently of HIF activation.

Keywords: Adipocytes; Differentiation; Gene expression; Hypoxia; Lipogenesis; Lipolysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • ATP Citrate (pro-S)-Lyase / genetics
  • ATP Citrate (pro-S)-Lyase / metabolism
  • Acetyl Coenzyme A / metabolism
  • Adipocytes / cytology
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adipogenesis / drug effects*
  • Adipogenesis / genetics
  • Animals
  • Cell Differentiation / drug effects
  • Cell Hypoxia
  • Citric Acid Cycle / drug effects
  • Citric Acid Cycle / genetics
  • Diacylglycerol O-Acyltransferase / genetics
  • Diacylglycerol O-Acyltransferase / metabolism
  • Dose-Response Relationship, Drug
  • Fatty Acid-Binding Proteins / genetics
  • Fatty Acid-Binding Proteins / metabolism
  • Gene Expression Regulation / drug effects*
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Lipid Droplets / chemistry
  • Lipid Droplets / drug effects
  • Lipogenesis / drug effects*
  • Lipogenesis / genetics
  • Lipolysis / drug effects*
  • Lipolysis / genetics
  • Mice
  • Oxygen / pharmacology*
  • Perilipin-1 / genetics
  • Perilipin-1 / metabolism
  • Signal Transduction
  • Sterol Esterase / genetics
  • Sterol Esterase / metabolism
  • Triglycerides / metabolism

Substances

  • Fabp4 protein, mouse
  • Fatty Acid-Binding Proteins
  • HIF1A protein, human
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Perilipin-1
  • Plin1 protein, mouse
  • Triglycerides
  • Acetyl Coenzyme A
  • DGAT2 protein, mouse
  • Diacylglycerol O-Acyltransferase
  • ATP Citrate (pro-S)-Lyase
  • Sterol Esterase
  • Oxygen