Molecular Mechanisms of Cellular Senescence in Neurodegenerative Diseases

被引:15
|
作者
Lee, He-Jin [1 ,2 ,6 ]
Yoon, Ye-Seul [1 ,2 ]
Lee, Seung-Jae [3 ,4 ,5 ]
机构
[1] Konkuk Univ, Dept Anat, Seoul 05029, South Korea
[2] Konkuk Univ, IBST, Seoul 05029, South Korea
[3] Seoul Natl Univ, Neurosci Res Inst, Convergence Res Ctr Dementia, Dept Biomed Sci,Coll Med, Seoul, South Korea
[4] Neuramedy Co Ltd, Seoul, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Biomed Sci, 103 Daehak Ro, Seoul 03080, South Korea
[6] Konkuk Univ, Sch Med, Dept Anat, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
cellular senescence; neurodegenerative diseases; protein aggregation; senolytic therapy; senescence-associated secretory phenotype; DEPENDENT KINASE INHIBITORS; DNA-DAMAGE RESPONSE; ALZHEIMERS-DISEASE; ALPHA-SYNUCLEIN; PARKINSONS-DISEASE; SECRETORY PHENOTYPE; BETA-GALACTOSIDASE; OXIDATIVE STRESS; LEWY BODIES; IN-VITRO;
D O I
10.1016/j.jmb.2023.168114
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
Neurodegenerative diseases, such as Alzheimer's and Parkinson's, are characterized by several patho-logical features, including selective neuronal loss, aggregation of specific proteins, and chronic inflamma-tion. 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 senes-cence is a cell state or fate in response to stimuli. It is typically associated with a series of changes in cel-lular 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 neurodegen-erative 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.(c) 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:16
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