Lab Anim Res.  2024 Dec;40(4):408-423. 10.1186/s42826-024-00224-4.

Hypoxia‑inducible factor‑1α‑deficient adipose‑tissue macrophages produce the heat to mediate lipolysis of white adipose tissue through uncoupling protein‑1

Affiliations
  • 1College of Veterinary Medicine, Seoul National University, Seoul 08826, Korea
  • 2Department of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 37673, Korea
  • 3Department of Nuclear Medicine, College of Medicine, Seoul National University, Seoul 03080, Korea
  • 4Department of Pathology, College of Medicine, Seoul National University, Seoul 03080, Korea
  • 5Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National Uni‑ versity, Seoul 08826, Korea
  • 6College of Medicine, Cancer Research Institute, Seoul National University, Seoul 03080, Korea
  • 7Department of Life Sciences, Ewha Womans University, Seoul 03760, Korea
  • 8Department of Chemistry, POSTECH, Pohang 37673, Korea
  • 9Department of Surgery, College of Medicine, Seoul National University, Seoul 03080, Korea

Abstract

Background
Uncoupling protein 1 (UCP1) is a proton uncoupler located across the mitochondrial membrane gener‑ ally involved in thermogenesis of brown adipose tissues. Although UCP1 is known to be strongly expressed in brown adipocytes, recent evidence suggest that white adipocytes can also express UCP1 under certain circumstances such as cold- or β-adrenergic receptor-stimulation, allowing them to acquire brown adipocyte-like features thereby becoming ’beige’ adipocytes.
Results
In this study, we report that UCP1 can be expressed in adipose-tissue macrophages (ATM) lacking func‑ tional hypoxia-inducible factor-1 (HIF-1) and this does not require cold- nor β-adrenergic receptor activation. By using myeloid-specific Hif-1α knockout (KO) mice, we observed that these mice were protected from diet-induced obesity and exhibited an improved thermogenic tolerance upon cold challenge. ATM isolated from white adipose tissues (WAT) of these mice fed with high fat diet exhibited significantly higher M2-polarization, decreased gly‑ colysis, increased mitochondrial functions and acetyl-CoA levels, along with increased expression of Ucp1, peroxisome proliferator activated receptor-gamma co-activator-1a, and others involved in histone acetylation. Consistent with the increased Ucp1 gene expression, these ATM produced a significant amount of heat mediating lipolysis of cocultured adipocytes liberating free fatty acid. Treating ATM with acetate, a substrate for acetyl-CoA synthesis was able to boost the heat production in wild-type or Hif-1α-deficient but not UCP1-deficient macrophages, indicating that UCP1 was necessary for the heat production in macrophages. Lastly, we observed a significant inverse correlation between the number of UCP1-expressing ATM in WAT and the body mass index of human individuals.
Conclusions
UCP1-expressing ATM produce the heat to mediate lipolysis of adipocytes, indicating that this can be a novel strategy to treat and prevent diet-induced obesity.

Keyword

Obesity; Uncoupling protein-1; Adipose-tissue macrophage; Heat; Lipolysis
Full Text Links
  • LAR
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2025 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr