The Effect of Pericellular Oxygen Levels on Proteomic Profile and Lipogenesis in 3T3-L1 Differentiated Preadipocytes Cultured on Gas-Permeable Cultureware

PLoS One. 2016 Mar 29;11(3):e0152382. doi: 10.1371/journal.pone.0152382. eCollection 2016.

Abstract

Pericellular oxygen concentration represents an important factor in the regulation of cell functions, including cell differentiation, growth and mitochondrial energy metabolism. Hypoxia in adipose tissue has been associated with altered adipokine secretion profile and suggested as a possible factor in the development of type 2 diabetes. In vitro experiments provide an indispensable tool in metabolic research, however, physical laws of gas diffusion make prolonged exposure of adherent cells to desired pericellular O2 concentrations questionable. The aim of this study was to investigate the direct effect of various O2 levels (1%, 4% and 20% O2) on the proteomic profile and triglyceride accumulation in 3T3-L1 differentiated preadipocytes using gas-permeable cultureware. Following differentiation of cells under desired pericellular O2 concentrations, cell lysates were subjected to two-dimensional gel electrophoresis and protein visualization using Coomassie blue staining. Spots showing differential expression under hypoxia were analyzed using matrix-assisted laser desorption/ionization mass spectrometry. All identified proteins were subjected to pathway analysis. We observed that protein expression of 26 spots was reproducibly affected by 4% and 1% O2 (17 upregulated and 9 downregulated). Pathway analysis showed that mitochondrial energy metabolism and triglyceride synthesis were significantly upregulated by hypoxia. In conclusion, this study demonstrated the direct effects of pericellular O2 levels on adipocyte energy metabolism and triglyceride synthesis, probably mediated through the reversed tricarboxylic acid cycle flux.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology*
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Animals
  • Cell Count
  • Cell Differentiation / drug effects*
  • Cells, Cultured
  • Citric Acid Cycle / drug effects
  • Down-Regulation / drug effects
  • Electrophoresis, Gel, Two-Dimensional
  • Gases / chemistry*
  • Lipids / biosynthesis
  • Lipogenesis / drug effects*
  • Mice
  • Oxygen / pharmacology*
  • Permeability
  • Proteomics*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Triglycerides / metabolism
  • Up-Regulation / drug effects

Substances

  • Gases
  • Lipids
  • Triglycerides
  • Oxygen

Grants and funding

This work was supported by Grant Agency of Czech Republic -GACR P304/13—27735S—JP (http://gacr.cz); Grant Agency of Charles University-GAUK 226214—MW (http://www.cuni.cz/UK-33.html); Specific University Research Grant- SVV 260165/2015—JP MW (http://www.cuni.cz/UK-3362.html); and The Ministry of Education, Youth and Sports of the Czech Republic- project LO1509 and Operational Program Prague – Competitiveness project (CZ.2.16/3.1.00/24023) supported by EU. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.