Department of Pharmacology, Research Institute for Basic Medical Science, School of Medicine, CHA University, CHA Bio Complex, 335 Pangyo, Bundang-gu, Seongnam-si, Gyeonggi-do, 13488, Republic of Korea.
Dementia Research Group, Korea Brain Research Institute, Daegu, Republic of Korea.
Transl Neurodegener. 2024 Feb 20;13(1):10. doi: 10.1186/s40035-024-00402-3.
Brain aging is a recognized risk factor for neurodegenerative diseases like Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease), but the intricate interplay between brain aging and the pathogenesis of these conditions remains inadequately understood. Cellular senescence is considered to contribute to cellular dysfunction and inflammaging. According to the threshold theory of senescent cell accumulation, the vulnerability to neurodegenerative diseases is associated with the rates of senescent cell generation and clearance within the brain. Given the role of microglia in eliminating senescent cells, the accumulation of senescent microglia may lead to the acceleration of brain aging, contributing to inflammaging and increased vulnerability to neurodegenerative diseases. In this review, we propose the idea that the senescence of microglia, which is notably vulnerable to aging, could potentially serve as a central catalyst in the progression of neurodegenerative diseases. The senescent microglia are emerging as a promising target for mitigating neurodegenerative diseases.
大脑老化是阿尔茨海默病、帕金森病和肌萎缩侧索硬化症(ALS,俗称“渐冻人症”)等神经退行性疾病的公认风险因素,但大脑老化与这些疾病发病机制之间的复杂相互作用仍了解不足。细胞衰老被认为会导致细胞功能障碍和炎症衰老。根据衰老细胞积累的阈值理论,大脑中衰老细胞的生成和清除率与神经退行性疾病的易感性相关。鉴于小胶质细胞在清除衰老细胞中的作用,衰老小胶质细胞的积累可能导致大脑老化加速,导致炎症衰老和神经退行性疾病易感性增加。在这篇综述中,我们提出了这样一种观点,即易受衰老影响的小胶质细胞的衰老可能是神经退行性疾病进展的核心催化剂。衰老的小胶质细胞作为一种有前途的治疗神经退行性疾病的靶点正在浮现。