Mastering organismal aging through the endoplasmic reticulum proteostasis network

被引:39
作者
Taylor, Rebecca C. [1 ]
Hetz, Claudio [2 ,3 ,4 ,5 ]
机构
[1] MRC Lab Mol Biol, Cambridge, England
[2] Ctr Gerosci Brain Hlth & Metab, Santiago, Chile
[3] Univ Chile, Biomed Neurosci Inst, Fac Med, Sect B,Second Floor,Independencia 1027,POB 70086, Santiago, Chile
[4] Univ Chile, Inst Biomed Sci, Program Cellular & Mol Biol, Santiago, Chile
[5] Buck Inst Res Aging, Novato, CA USA
基金
英国医学研究理事会;
关键词
aging; autophagy; cell‐ nonautonomous; ER stress; protein misfolding; proteostasis; UNFOLDED PROTEIN RESPONSE; ER-STRESS; LIFE-SPAN; GENE-EXPRESSION; QUALITY CONTROL; HOMEOSTASIS; PATHWAY; LONGEVITY; CELLS; INFLAMMATION;
D O I
10.1111/acel.13265
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aging process is characterized by a progressive decline in the function of most tissues, representing the main risk factor in the development of a variety of human diseases. Studies in multiple animal models have demonstrated that interventions that improve the capacity to maintain endoplasmic reticulum (ER) proteostasis prolong life and healthspan. ER stress is monitored by the unfolded protein response (UPR), a signaling pathway that mediates adaptive processes to restore proteostasis or the elimination of damaged cells by apoptosis. Here, we discuss recent advances in understanding the significance of the UPR to aging and its implications for the maintenance of cell physiology of various cell types and organs. The possible benefits of targeting the UPR to extend healthspan and reduce the risk of developing age-related diseases are also discussed.
引用
收藏
页数:12
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