Maternal Brown Fat Thermogenesis Programs Glucose Tolerance in the Male Offspring

Cell Rep. 2020 Nov 3;33(5):108351. doi: 10.1016/j.celrep.2020.108351.

Abstract

Environmental temperature is a driving factor in evolution, and it is commonly assumed that metabolic adaptations to cold climates are the result of transgenerational selection. Here, we show in mice that even minor changes in maternal thermogenesis alter the metabolic phenotype already in the next generation. Male offspring of mothers genetically lacking brown adipose tissue (BAT) thermogenesis display increased lean mass and improved glucose tolerance as adults, while females are unaffected. The phenotype is replicated in offspring of mothers kept at thermoneutrality; conversely, mothers with higher gestational BAT thermogenesis produce male offspring with reduced lean mass and impaired glucose tolerance. Running-wheel exercise reverses the offspring's metabolic impairments, pointing to the muscle as target of these fetal programming effects. Our data demonstrate that gestational BAT activation negatively affects metabolic health of the male offspring; however, these unfavorable fetal programming effects may be negated by active lifestyle.

Keywords: brown adipose tissue; cold acclimation; environment; fetal programming; gestation; pregnancy; temperature; thermogenesis; thermoneutrality; uncoupling protein 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / physiology*
  • Animals
  • Energy Metabolism / physiology
  • Female
  • Glucose / metabolism*
  • Homeostasis
  • Humans
  • Male
  • Metabolomics
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Physical Conditioning, Animal
  • Pregnancy
  • Temperature
  • Thermogenesis / physiology*
  • Uncoupling Protein 1 / deficiency
  • Uncoupling Protein 1 / metabolism

Substances

  • Uncoupling Protein 1
  • Glucose