Institute for Endocrinology and Diabetes-Molecular Endocrinology, Center of Brain Behavior & Metabolism, University of Lübeck, 23562 Lübeck, Germany.
Institute for Human Genetics-Epigenetics and Metabolism, Deutsches Zentrum für Diabetesforschung, Center of Brain Behavior & Metabolism, University of Lübeck, 23562 Lübeck, Germany.
Cell Rep. 2020 Nov 3;33(5):108351. doi: 10.1016/j.celrep.2020.108351.
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.
环境温度是进化的驱动因素,人们普遍认为,对寒冷气候的代谢适应是跨代选择的结果。在这里,我们在小鼠中表明,即使母体产热的微小变化也会改变下一代的代谢表型。缺乏棕色脂肪组织(BAT)产热的母亲的雄性后代在成年后表现出增加的瘦体重和改善的葡萄糖耐量,而雌性则不受影响。这种表型在保持在热中性的母亲的后代中得到复制;相反,具有更高妊娠 BAT 产热的母亲会产生瘦体重减少和葡萄糖耐量受损的雄性后代。跑步轮运动逆转了后代的代谢损伤,表明肌肉是这些胎儿编程效应的靶标。我们的数据表明,妊娠期间 BAT 的激活会对雄性后代的代谢健康产生负面影响;然而,通过积极的生活方式,这些不利的胎儿编程效应可能会被抵消。