Redox regulation of the insulin signalling pathway

被引:56
作者
Lennicke, Claudia [1 ,2 ]
Cocheme, Helena M. [1 ,2 ]
机构
[1] MRC London Inst Med Sci, Du Cane Rd, London W12 0NN, England
[2] Imperial Coll London, Inst Clin Sci, Hammersmith Hosp Campus,Du Cane Rd, London W12 0NN, England
来源
REDOX BIOLOGY | 2021年 / 42卷
基金
英国医学研究理事会;
关键词
Redox regulation; ROS; Insulin signalling; Cysteine post-translational modification; FOXO; NRF2; Type-2; diabetes; TYROSINE-PHOSPHATASE; 1B; HIGH-FAT DIET; TUMOR-SUPPRESSOR PTEN; TRANSCRIPTION FACTOR NRF2; HYDROGEN-PEROXIDE; REACTIVE OXYGEN; OXIDATIVE STRESS; REVERSIBLE INACTIVATION; PROTEIN PHOSPHATASE; MOLECULAR-MECHANISM;
D O I
10.1016/j.redox.2021.101964
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 H2O2, have been recognised as insulin-mimetics. Treatment of cells with insulin leads to increased intracellular H2O2 levels affecting the activity of downstream signalling components, thereby amplifying insulin-mediated signal transduction. Specific molecular targets of insulin-stimulated H2O2 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.
引用
收藏
页数:14
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