The Peroxisome Proliferator-Activated Receptor alpha is dispensable for cold-induced adipose tissue browning in mice

Merel Defour, Wieneke Dijk, Philip Ruppert, Emmani B. M. Nascimento, Patrick Schrauwen, Sander Kersten*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

26 Citations (Web of Science)

Abstract

Objective: Chronic cold exposure causes white adipose tissue (WAT) to adopt features of brown adipose tissue (BAT), a process known as browning. Previous studies have hinted at a possible role for the transcription factor Peroxisome Proliferator-Activated Receptor alpha (PPAR alpha) in cold-induced browning. Here we aimed to investigate the importance of PPAR alpha in driving transcriptional changes during cold-induced browning in mice.

Methods: Male wildtype and PPAR alpha-/- mice were housed at thermoneutrality (28 degrees C) or cold (5 degrees C) for 10 days. Whole genome expression analysis was performed on inguinal WAT. In addition, other analyses were carried out. Whole genome expression data of livers of wildtype and PPAR alpha-/- mice fasted for 24 h served as positive control for PPAR alpha-dependent gene regulation.

Results: Cold exposure increased food intake and decreased weight of BAT and WAT to a similar extent in wildtype and PPAR alpha-/- mice. Except for plasma non-esterified fatty acids, none of the cold-induced changes in plasma metabolites were dependent on PPAR alpha genotype. Histological analysis of inguinal WAT showed clear browning upon cold exposure but did not reveal any morphological differences between wildtype and PPAR alpha-/- mice. Transcriptomics analysis of inguinal WAT showed a marked effect of cold on overall gene expression, as revealed by principle component analysis and hierarchical clustering. However, wildtype and PPAR alpha-/- mice clustered together, even after cold exposure, indicating a similar overall gene expression profile in the two genotypes. Pathway analysis revealed that cold upregulated pathways involved in energy usage, oxidative phosphorylation, and fatty acid beta-oxidation to a similar extent in wildtype and PPAR alpha-/- mice. Furthermore, cold-mediated induction of genes related to thermogenesis such as Ucp1, Elovl3, Cox7a1, Cox8, and Cidea, as well as many PPAR target genes, was similar in wildtype and PPAR alpha-/- mice. Finally, pharmacological PPAR alpha activation had a minimal effect on expression of cold-induced genes in murine WAT.

Conclusion: Cold-induced changes in gene expression in inguinal WAT are unaltered in mice lacking PPAR alpha, indicating that PPAR alpha is dispensable for cold-induced browning. (C) 2018 The Authors. Published by Elsevier GmbH.

Original languageEnglish
Pages (from-to)39-54
Number of pages16
JournalMolecular Metabolism
Volume10
DOIs
Publication statusPublished - Apr 2018

Keywords

  • Cold
  • Adipose tissue browning
  • PPAR alpha
  • Transcriptomics
  • RETINOID-X-RECEPTOR
  • PPAR-GAMMA
  • GENE-EXPRESSION
  • FATTY-ACIDS
  • UNCOUPLING PROTEIN-1
  • LIPID-METABOLISM
  • OBESE MICE
  • ADIPOCYTES
  • LIVER
  • THIAZOLIDINEDIONE

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