平衡
内分泌学
内科学
胰岛素抵抗
骨骼肌
脂肪组织
脂质代谢
葡萄糖稳态
白色脂肪组织
生物
焊剂(冶金)
脂毒性
胰岛素
化学
医学
有机化学
作者
Liyan Fan,David R. Sweet,Domenick A. Prosdocimo,Vinesh Vinayachandran,E. Ricky Chan,Rongli Zhang,Olga Ilkayeva,Yuan Lü,Komal S. Keerthy,Chloe E. Booth,Christopher B. Newgard,Mukesh K. Jain
摘要
Skeletal muscle is a major determinant of systemic metabolic homeostasis that plays a critical role in glucose metabolism and insulin sensitivity. By contrast, despite being a major user of fatty acids, and evidence that muscular disorders can lead to abnormal lipid deposition (e.g., nonalcoholic fatty liver disease in myopathies), our understanding of skeletal muscle regulation of systemic lipid homeostasis is not well understood. Here we show that skeletal muscle Krüppel-like factor 15 (KLF15) coordinates pathways central to systemic lipid homeostasis under basal conditions and in response to nutrient overload. Mice with skeletal muscle-specific KLF15 deletion demonstrated (a) reduced expression of key targets involved in lipid uptake, mitochondrial transport, and utilization, (b) elevated circulating lipids, (c) insulin resistance/glucose intolerance, and (d) increased lipid deposition in white adipose tissue and liver. Strikingly, a diet rich in short-chain fatty acids bypassed these defects in lipid flux and ameliorated aspects of metabolic dysregulation. Together, these findings establish skeletal muscle control of lipid flux as critical to systemic lipid homeostasis and metabolic health.
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