In vivo emergence of beige-like fat in chickens as physiological adaptation to cold environments

Amino Acids. 2021 Mar;53(3):381-393. doi: 10.1007/s00726-021-02953-5. Epub 2021 Feb 17.

Abstract

While it has been hypothesized that brown adipocytes responsible for mammalian thermogenesis are absent in birds, the existence of beige fat has yet to be studied directly. The present study tests the hypothesis that beige fat emerges in birds as a mechanism of physiological adaptation to cold environments. Subcutaneous neck adipose tissue from cold-acclimated or triiodothyronine (T3)-treated chickens exhibited increases in the expression of avian uncoupling protein (avUCP, an ortholog of mammalian UCP2 and UCP3) gene and some known mammalian beige adipocyte-specific markers. Morphological characteristics of white adipose tissues of treated chickens showed increased numbers of both small and larger clusters of multilocular fat cells within the tissues. Increases in protein levels of avUCP and mitochondrial marker protein, voltage-dependent anion channel, and immunohistochemical analysis for subcutaneous neck fat revealed the presence of potentially thermogenic mitochondria-rich cells. This is the first evidence that the capacity for thermogenesis may be acquired by differentiating adipose tissue into beige-like fat for maintaining temperature homeostasis in the subcutaneous fat 'neck warmer' in chickens exposed to a cold environment.

Keywords: Avian models; Beige fat; Cold adaptation; Thermogenesis; avUCP.

MeSH terms

  • Abdominal Fat / cytology
  • Abdominal Fat / metabolism
  • Acclimatization / physiology*
  • Adipocytes, Beige / metabolism
  • Adipose Tissue / metabolism
  • Animals
  • Body Weight
  • Chickens / physiology*
  • Cold Temperature
  • Eating
  • Mitochondria / metabolism
  • Neck / physiology
  • Subcutaneous Fat / cytology
  • Subcutaneous Fat / drug effects
  • Subcutaneous Fat / metabolism*
  • Thermogenesis / drug effects
  • Triiodothyronine / pharmacology
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism
  • Voltage-Dependent Anion Channels / metabolism

Substances

  • Uncoupling Protein 1
  • Voltage-Dependent Anion Channels
  • Triiodothyronine