Paracrine stimulation of brown adipose tissue vascularization by adipocyte O-GlcNAc signaling

Cell Rep. 2025 Dec 23;44(12):116678. doi: 10.1016/j.celrep.2025.116678. Epub 2025 Dec 11.

Abstract

Brown adipose tissue (BAT) is extensively vascularized, which is essential for its physiological activities. The molecular mechanism that underpins BAT vascularization, however, remains poorly understood. This study presents evidence that acute cold exposure induces an elevation in total protein O-linked β-N-acetylglucosamine modification (O-GlcNAcylation) in BAT. Ablation of O-GlcNAc transferase in brown adipocytes drastically impairs BAT vascularization. Mechanistic studies demonstrate that O-GlcNAcylation of specificity protein 1 in brown adipocytes enhances its transcriptional activity toward kielin/chordin-like protein (Kcp). Secreted KCP subsequently promotes BAT angiogenesis by paracrine activation of bone morphogenetic protein signaling. Furthermore, boosting O-GlcNAc signaling with glucosamine supplementation effectively augments BAT vascularization and thermogenesis. These findings thus uncover a previously unrecognized role of adipocyte O-GlcNAc signaling in the metabolism-driven regulation of BAT vascularization and function.

Keywords: BMP signaling; CP: metabolism; KCP; O-GlcNAc; brown adipose tissue; vascular system.

MeSH terms

  • Acetylglucosamine* / metabolism
  • Adipocytes / metabolism
  • Adipocytes, Brown* / metabolism
  • Adipose Tissue, Brown* / blood supply
  • Adipose Tissue, Brown* / metabolism
  • Animals
  • Male
  • Mice
  • Mice, Inbred C57BL
  • N-Acetylglucosaminyltransferases / genetics
  • N-Acetylglucosaminyltransferases / metabolism
  • Neovascularization, Physiologic*
  • Paracrine Communication*
  • Signal Transduction
  • Thermogenesis

Substances

  • Acetylglucosamine
  • N-Acetylglucosaminyltransferases
  • O-GlcNAc transferase