Sestrins are Gatekeepers in the Way from Stress to Aging and Disease

被引:0
|
作者
Dalina, A. A. [1 ,2 ]
Kovaleva, I. E. [3 ]
Budanov, A. V. [1 ,2 ]
机构
[1] Russian Acad Sci, Engelhardt Inst Mol Biol, Moscow 119991, Russia
[2] Trinity Coll Dublin, Dublin 2, Ireland
[3] Lomonosov Moscow State Univ, Belozersky Inst Phys & Chem Biol, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
Sesn1; Sesn2; Sesn3; mTOR; autophagy; aging; stress; cell death; UNFOLDED PROTEIN RESPONSE; TUMOR-SUPPRESSOR; INHIBIT MTORC1; CELL CARCINOMA; CHROMOSOME; 1P; RAG GTPASES; ER STRESS; ACTIVATION; ACID; METABOLISM;
D O I
10.1134/S0026893318060043
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
Sestrins belong to a family of evolutionary conserved proteins which are found in the majority of animal species. While invertebrate genomes contain only one sestrin gene, mammalian and other vertebrate genomes comprise three highly homologous genes that encode Sestrin 1, 2 and 3 proteins (Sesn1, Sesn2 and Sesn3). Sestrins are activated in response to a variety of stimuli and trigger metabolic shifts promoting cell survival under stress conditions. Although cellular stress within an organism is often caused by external stimuli it can be induced by excess of cytokines, chemokines, reactive oxygen species which are produced during aberrant metabolic or immune processes and are involved in regulation of cell physiological states including cell death. Activation of sestrins facilitates cell adaptation to stress through stimulation of antioxidant response and autophagy through regulation of the signaling pathways mediated by AMPK and mTOR kinases. These activities are involved in protection of the organism during physical exercise and certain level of sestrins activity contributes to the development of age-related diseases. However, prolonged activation of sestrins under chronic stress may cause negative effects for the organism.
引用
收藏
页码:823 / 835
页数:13
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