脂毒性
线粒体
细胞生物学
氧化应激
胞吐
生物
活性氧
细胞凋亡
胰岛素
胰岛素抵抗
分泌物
内分泌学
遗传学
作者
Sachin Supale,Ning Li,Thierry Brun,Pierre Maechler
标识
DOI:10.1016/j.tem.2012.06.002
摘要
In pancreatic β cells, mitochondria play a central role in coupling glucose metabolism to insulin exocytosis, thereby ensuring strict control of glucose-stimulated insulin secretion. Defects in mitochondrial function impair this metabolic coupling, and ultimately promote apoptosis and β cell death. Various factors have been identified that may contribute to mitochondrial dysfunction. In this review we address the emerging concept of complex links between these factors. We also discuss the role of the mitochondrial genome and mutations associated with diabetes, the effect of oxidative stress and reactive oxygen species, the sensitivity of mitochondria to lipotoxicity, and the adaptive dynamics of mitochondrial morphology. Better comprehension of the molecular mechanisms contributing to mitochondrial dysfunction will help drive the development of effective therapeutic approaches.
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