Cao Sheng-nan, Bao Xiu-qi, Sun Hua, Zhang Dan
State Key Laboratory of Natural Products and Functions,Institute of Materia Medica,CAMS and PUMC,Beijing 100050,China;
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2016 Apr;38(2):228-33. doi: 10.3881/j.issn.1000-503X.2016.02.018.
Microglia are the resident innate immune cells in the brain. Under endogenous or exogenous stimulates, they become activated and play an important role in the neurodegenerative diseases. Microglial phagocytosis is a process of receptor-mediated engulfment and degradation of apoptotic cells. In addition, microglia can phagocyte brain-specific cargo, such as myelin debris and abnormal protein aggregation. However, recent studies have shown that microglia can also phagocyte stressed-but-viable neurons, causing loss of neurons in the brain. Thus, whether microglial phagocytosis is beneficial or not in neurodegenerative disease remains controversial. This article reviews microglial phagocytosis related mechanisms and its potential roles in neurodegenerative diseases, with an attempt to provide new insights in the treatment of neurodegenerative diseases.
小胶质细胞是大脑中的常驻固有免疫细胞。在内源性或外源性刺激下,它们被激活并在神经退行性疾病中发挥重要作用。小胶质细胞吞噬作用是一个受体介导的吞噬和降解凋亡细胞的过程。此外,小胶质细胞可以吞噬脑特异性物质,如髓鞘碎片和异常蛋白质聚集物。然而,最近的研究表明,小胶质细胞也可以吞噬应激但仍存活的神经元,导致大脑中的神经元丢失。因此,小胶质细胞吞噬作用在神经退行性疾病中是否有益仍存在争议。本文综述了小胶质细胞吞噬作用的相关机制及其在神经退行性疾病中的潜在作用,试图为神经退行性疾病的治疗提供新的见解。