脂肪细胞
过剩4
脂肪生成
胰岛素受体
葡萄糖稳态
生物
胰岛素抵抗
葡萄糖摄取
碳水化合物代谢
胰岛素
葡萄糖转运蛋白
代谢途径
细胞生物学
内科学
内分泌学
生物化学
作者
C Martinez Calejman,W G Doxsey,D J Fazakerley,D A Guertin
标识
DOI:10.1016/j.tibs.2022.02.009
摘要
Insulin stimulates glucose uptake into adipocytes via mTORC2/AKT signaling and GLUT4 translocation and directs glucose carbons into glycolysis, glycerol for TAG synthesis, and de novo lipogenesis. Adipocyte insulin resistance is an early indicator of type 2 diabetes in obesity, a worldwide health crisis. Thus, understanding the interplay between insulin signaling and central carbon metabolism pathways that maintains adipocyte function, blood glucose levels, and metabolic homeostasis is critical. While classically viewed through the lens of individual enzyme–substrate interactions, advances in mass spectrometry are beginning to illuminate adipocyte signaling and metabolic networks on an unprecedented scale, yet this is just the tip of the iceberg. Here, we review how ‘omics approaches help to elucidate adipocyte insulin action in cellular time and space.
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