未折叠蛋白反应
内质网
生物
细胞生物学
平衡
生态学
计算生物学
作者
Ashley E. Frakes,Andrew Dillin
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2017-06-01
卷期号:66 (6): 761-771
被引量:266
标识
DOI:10.1016/j.molcel.2017.05.031
摘要
Life is stressful. Organisms are repeatedly exposed to stressors that disrupt protein homeostasis (proteostasis), resulting in protein misfolding and aggregation. To sense and respond to proteotoxic perturbations, cells have evolved compartment-specific stress responses, such as the unfolded protein response of the endoplasmic reticulum (UPRER). However, UPRER function is impaired with age, which, we propose, creates a permissive environment for protein aggregation, unresolved ER stress, and chronic inflammation. Understanding age-related changes to the UPRER will provide new avenues for therapeutic intervention in metabolic disease, neurodegeneration, and aging.
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