蛋白质稳态
衰老
表型
生物
细胞模型
细胞衰老
细胞生物学
氧化应激
老化
机制(生物学)
神经退行性变
炎症
活性氧
神经科学
疾病
遗传学
免疫学
医学
基因
生物化学
细胞培养
病理
哲学
认识论
作者
He-Jin Lee,Ye-Seul Yoon,Seung‐Jae Lee
标识
DOI:10.1016/j.jmb.2023.168114
摘要
Neurodegenerative diseases, such as Alzheimer’s and Parkinson’s, are characterized by several pathological features, including selective neuronal loss, aggregation of specific proteins, and chronic inflammation. Aging is the most critical risk factor of these disorders. However, the mechanism by which aging contributes to the pathogenesis of neurodegenerative diseases is not clearly understood. Cellular senescence is a cell state or fate in response to stimuli. It is typically associated with a series of changes in cellular phenotypes such as abnormal cellular metabolism and proteostasis, reactive oxygen species (ROS) production, and increased secretion of certain molecules via senescence-associated secretory phenotype (SASP). In this review, we discuss how cellular senescence contributes to brain aging and neurodegenerative diseases, and the relationship between protein aggregation and cellular senescence. Finally, we discuss the potential of senescence modifiers and senolytics in the treatment of neurodegenerative diseases.
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