脂肪细胞
生物
组学
胰岛素
计算生物学
生物信息学
内分泌学
生物化学
脂肪组织
作者
Camila Martínez Calejman,Will G. Doxsey,Daniel J. Fazakerley,David 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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