Dana-Farber Cancer Institute and Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2012 Jun 12;109(24):9635-40. doi: 10.1073/pnas.1207287109. Epub 2012 May 29.
Reduced peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) expression and mitochondrial dysfunction in adipose tissue have been associated with obesity and insulin resistance. Whether this association is causally involved in the development of insulin resistance or is only a consequence of this condition has not been clearly determined. Here we studied the effects of adipose-specific deficiency of PGC-1α on systemic glucose homeostasis. Loss of PGC-1α in white fat resulted in reduced expression of the thermogenic and mitochondrial genes in mice housed at ambient temperature, whereas gene expression patterns in brown fat were not altered. When challenged with a high-fat diet, insulin resistance was observed in the mutant mice, characterized by reduced suppression of hepatic glucose output. Resistance to insulin was also associated with an increase in circulating lipids, along with a decrease in the expression of genes regulating lipid metabolism and fatty acid uptake in adipose tissues. Taken together, these data demonstrate a critical role for adipose PGC-1α in the regulation of glucose homeostasis and a potentially causal involvement in the development of insulin resistance.
脂肪组织中过氧化物酶体增殖物激活受体γ共激活因子-1α(PGC-1α)表达减少和线粒体功能障碍与肥胖和胰岛素抵抗有关。这种关联是否与胰岛素抵抗的发生有因果关系,或者只是这种情况的结果,尚不清楚。在这里,我们研究了脂肪组织特异性 PGC-1α 缺乏对全身葡萄糖稳态的影响。在环境温度下饲养的小鼠中,白色脂肪中 PGC-1α 的缺失导致产热和线粒体基因的表达减少,而棕色脂肪中的基因表达模式没有改变。当用高脂肪饮食挑战时,突变小鼠表现出胰岛素抵抗,其特征是肝葡萄糖输出的抑制减少。对胰岛素的抵抗也与循环脂质的增加以及调节脂肪组织中脂质代谢和脂肪酸摄取的基因表达减少有关。综上所述,这些数据表明脂肪组织 PGC-1α 在调节葡萄糖稳态方面起着关键作用,并可能在胰岛素抵抗的发生中起因果关系。