Differential regulation of uncoupling protein gene homologues in multiple tissues of hibernating ground squirrels

Am J Physiol. 1998 Oct;275(4):R1232-8. doi: 10.1152/ajpregu.1998.275.4.R1232.

Abstract

Nonshivering thermogenesis in brown adipose tissue (BAT) provides heat through activation of a mitochondrial uncoupling protein (UCP1), which causes futile electron transport cycles without the production of ATP. Recent discovery of two molecular homologues, UCP2, expressed in multiple tissues, and UCP3, expressed in muscle, has resulted in investigation of their roles in thermoregulatory physiology and energy balance. To determine the expression pattern of Ucp homologues in hibernating mammals, we compared relative mRNA levels of Ucp1, -2, and -3 in BAT, white adipose tissue (WAT), and skeletal muscle of arctic ground squirrels (Spermophilus parryii) hibernating at different ambient and body temperatures, with levels determined in tissues from ground squirrels not in hibernation. Here we report significant increases in mRNA levels for Ucp2 in WAT (1. 6-fold) and Ucp3 in skeletal muscle (3-fold) during hibernation. These results indicate the potential for a role of UCP2 and UCP3 in thermal homeostasis during hibernation and indicate that parallel mechanisms and multiple tissues could be important for nonshivering thermoregulation in mammals.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipose Tissue / metabolism*
  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Body Temperature
  • Body Temperature Regulation*
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics*
  • Gene Expression Regulation*
  • Hibernation / physiology*
  • Ion Channels
  • Kidney / metabolism
  • Liver / metabolism
  • Membrane Proteins / biosynthesis
  • Membrane Proteins / genetics*
  • Membrane Transport Proteins*
  • Mitochondria / metabolism
  • Mitochondrial Proteins*
  • Muscle, Skeletal / metabolism*
  • Organ Specificity
  • Protein Biosynthesis
  • Proteins / genetics*
  • Sciuridae / physiology*
  • Seasons
  • Temperature
  • Uncoupling Protein 1
  • Uncoupling Protein 2
  • Uncoupling Protein 3

Substances

  • Carrier Proteins
  • Ion Channels
  • Membrane Proteins
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • Proteins
  • Uncoupling Protein 1
  • Uncoupling Protein 2
  • Uncoupling Protein 3