Chronic Fatty Acid Depletion Induces Uncoupling Protein 1 (UCP1) Expression to Coordinate Mitochondrial Inducible Proton Leak in a Human-Brown-Adipocyte Model

Cells. 2022 Jun 27;11(13):2038. doi: 10.3390/cells11132038.

Abstract

Thermogenic brown fat contributes to metabolic health in adult humans. Obese conditions are known to repress adipose-tissue browning and its activity. Herein, we found that chronic fatty acid (FA) depletion induced uncoupling protein 1 (UCP1) expression in the chemical-compound-induced brown adipocytes (ciBAs). The ciBAs, converted from human dermal fibroblasts under FA-free conditions, had low intracellular triglyceride levels and strongly activated UCP1 expression. Prolonged treatment with carnitine also reduced triglyceride accumulation and induced UCP1 expression. Transcriptome analysis revealed that the UCP1 induction was accompanied by the activation of lipid metabolic genes. The FA-depleted conditions repressed mitochondrial proton-leak activity and mitochondrial membrane potential (MMP), despite maintaining a high UCP1 expression. The evidence suggested that UCP1 expression was induced to compensate for the proton-leak activity under low MMP. Our study reports a regulatory mechanism underlying UCP1 expression and mitochondrial-energy status in human brown adipocytes under different nutritional conditions.

Keywords: human brown adipocytes; lipid metabolism; mitochondria; obesity; transcriptome analysis; uncoupling protein 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown* / metabolism
  • Adipose Tissue, Brown / metabolism
  • Energy Metabolism
  • Fatty Acids / metabolism
  • Humans
  • Mitochondrial Proteins / metabolism
  • Protons*
  • Triglycerides / metabolism
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism

Substances

  • Fatty Acids
  • Mitochondrial Proteins
  • Protons
  • Triglycerides
  • UCP1 protein, human
  • Uncoupling Protein 1

Grants and funding

This research was funded, for Y.T., by JSPS KAKENHI (Grant Number JP21K12669), the Takeda Science Foundation, and the Lotte Research Promotion Grant.