Differential mitochondrial adaptation and FNDC5 production in brown and white adipose tissue in response to cold and obesity

Obesity (Silver Spring). 2024 Nov;32(11):2120-2134. doi: 10.1002/oby.24132. Epub 2024 Sep 26.

Abstract

Objective: Fibronectin type III domain-containing protein 5 (FNDC5) modulates adipocyte metabolism by increasing white and brown adipose tissue (WAT and BAT) browning and activity, respectively. We investigated whether FNDC5 can regulate visceral WAT and BAT adaptive thermogenesis by improving mitochondrial homeostasis in response to cold and obesity.

Methods: Adipose tissue expression of FNDC5 and factors involved in mitochondrial homeostasis were determined in patients with normal weight and obesity (n = 159) and in rats with diet-induced obesity after 1 week of cold exposure (n = 61). The effect of different FNDC5 concentrations on mitochondrial biogenesis, dynamics, and mitophagy was evaluated in vitro in human adipocytes.

Results: In human visceral adipocytes, FNDC5/irisin triggered mitochondrial biogenesis (TFAM) and fusion (MFN1, MFN2, and OPA1) while inhibiting peripheral fission (DNM1L and FIS1) and mitophagy (PINK1 and PRKN). Circulating and visceral WAT expression of FNDC5 was decreased in patients and experimental animals with obesity, whereas its receptor, integrin αV, was upregulated. Obesity increased mitochondrial fusion while decreasing mitophagy in visceral WAT from patients and rats. By contrast, in rat BAT, an upregulation of Fndc5 and genes involved in mitochondrial biogenesis and fission was observed. Cold exposure promoted mitochondrial biogenesis and healthy peripheral fission while repressing Fndc5 expression and mitophagy in BAT from rats.

Conclusions: Depot differences in FNDC5 production and mitochondrial adaptations in response to obesity and cold might indicate a self-regulatory mechanism to control thermogenesis in response to energy needs.

MeSH terms

  • Adaptation, Physiological
  • Adipocytes / metabolism
  • Adipose Tissue, Brown* / metabolism
  • Adipose Tissue, White* / metabolism
  • Adult
  • Animals
  • Cold Temperature*
  • Female
  • Fibronectins* / genetics
  • Fibronectins* / metabolism
  • Humans
  • Male
  • Middle Aged
  • Mitochondria* / metabolism
  • Mitochondrial Dynamics
  • Mitophagy*
  • Obesity* / metabolism
  • Organelle Biogenesis
  • Rats
  • Thermogenesis*

Substances

  • Fibronectins
  • FNDC5 protein, human
  • FNDC5 protein, rat