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蛋白质动态平衡与神经退行性变中的衰老。

Protein homeostasis and aging in neurodegeneration.

机构信息

Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

出版信息

J Cell Biol. 2010 Sep 6;190(5):719-29. doi: 10.1083/jcb.201005144.

Abstract

Genetic and environmental factors responsible for numerous neurodegenerative diseases vary between disorders, yet age remains a universal risk factor. Age-associated decline in protein homeostasis, or proteostasis, enables disease-linked proteins to adopt aberrant tertiary structures, accumulate as higher-ordered aggregates, and cause a myriad of cellular dysfunctions and neuronal death. However, recent findings suggest that the assembly of disease proteins into tightly ordered aggregates can significantly delay proteotoxic onset. Furthermore, manipulation of metabolic pathways through key signaling components extends lifespan, bolsters proteostasis networks, and delays the onset of proteotoxicity. Thus, understanding the relationship between proteostasis and aging has provided important insights into neurodegeneration.

摘要

遗传和环境因素导致许多神经退行性疾病各不相同,但年龄仍然是普遍的风险因素。与年龄相关的蛋白质平衡或蛋白质稳态的下降使与疾病相关的蛋白质能够采用异常的三级结构,聚集成更高阶的聚集体,并导致多种细胞功能障碍和神经元死亡。然而,最近的研究结果表明,疾病蛋白组装成紧密有序的聚集体可以显著延迟毒性蛋白的产生。此外,通过关键信号成分对代谢途径的操纵可以延长寿命,增强蛋白质稳态网络,并延迟毒性蛋白的产生。因此,了解蛋白质稳态和衰老之间的关系为神经退行性变提供了重要的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c65e/2935559/6b1ee4dbd4f5/JCB_201005144_RGB_Fig1.jpg

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