MRC London Institute of Medical Sciences, Du Cane Road, London, W12 0NN, UK; Institute of Clinical Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
MRC London Institute of Medical Sciences, Du Cane Road, London, W12 0NN, UK; Institute of Clinical Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.
Redox Biol. 2021 Jun;42:101964. doi: 10.1016/j.redox.2021.101964. Epub 2021 Apr 2.
The peptide hormone insulin is a key regulator of energy metabolism, proliferation and survival. Binding of insulin to its receptor activates the PI3K/AKT signalling pathway, which mediates fundamental cellular responses. Oxidants, in particular HO, have been recognised as insulin-mimetics. Treatment of cells with insulin leads to increased intracellular HO levels affecting the activity of downstream signalling components, thereby amplifying insulin-mediated signal transduction. Specific molecular targets of insulin-stimulated HO include phosphatases and kinases, whose activity can be altered via redox modifications of critical cysteine residues. Over the past decades, several of these redox-sensitive cysteines have been identified and their impact on insulin signalling evaluated. The aim of this review is to summarise the current knowledge on the redox regulation of the insulin signalling pathway.
肽激素胰岛素是能量代谢、增殖和存活的关键调节剂。胰岛素与其受体结合激活 PI3K/AKT 信号通路,介导基本的细胞反应。氧化剂,特别是 HO,已被认为是胰岛素模拟物。用胰岛素处理细胞会导致细胞内 HO 水平升高,影响下游信号成分的活性,从而放大胰岛素介导的信号转导。胰岛素刺激的 HO 的特定分子靶标包括磷酸酶和激酶,其活性可以通过关键半胱氨酸残基的氧化还原修饰来改变。在过去的几十年中,已经鉴定出其中的几个氧化还原敏感半胱氨酸,并评估了它们对胰岛素信号转导的影响。本文综述了胰岛素信号通路的氧化还原调控的最新知识。