宁波大学医学院,浙江省病理生理重点实验室,宁波 315211
R741;R338
Zhejiang provincial key laboratory of pathophysiology, school of medicine, ningbo university, Ningbo, 315211, China
阿尔茨海默病(Alzheimer"s disease, AD)是最常见的中枢神经系统退行性疾病,其发病机制复杂,至今仍未完全阐明. 最近的研究表明,小胶质细胞过度激活、炎症因子的过度产生与AD的发病密切相关. 小胶质细胞受体及下游通路的异常调节可导致AD患者及AD实验动物的免疫失衡. 天然小分子化合物通过激活小胶质细胞的抑炎受体,抑制促炎受体,或调节Aβ清除受体,可逆转免疫失衡. 本文综述了小胶质细胞在AD慢性炎症中的作用机制,并总结天然小分子化合物通过调节小胶质细胞受体及其下游通路在AD免疫稳态中的有益作用.
Alzheimer's disease (AD) is the most common neurodegenerative disorders of the central nervous system (CNS). Its pathogenesis is complex and needs to be further studied. Recent findings have shown that inflammation, which is characterized by the excessive activation of microglias to produce inflammatory factors, is closely related to the pathogenesis of AD. Improper regulation of microglial receptors and their downstream pathways impair immune homeostasis in AD patients and AD experimental animals. Natural small-molecule compounds reverse the immune imbalance and retard the progresses of AD via inhibting the microglial pro-inflammatory receptors, activating microglial anti-inflammatory receptors and regulating the receptors involved in Aβ clearance. In this paper, we reviewed the mechanisms of chronic inflammation caused by microglias in AD, and summarized the beneficial effects of natural small-molecule compounds in AD immune homeostasis by regulating microglial receptors and their downstream pathways.
曹妍梓,王钦文,杨梦洁,鲍荣荣,徐淑君.天然小分子化合物调节小胶质细胞预防阿尔茨海默病免疫失衡*[J].生物化学与生物物理进展,2020,47(8):712-728
复制生物化学与生物物理进展 ® 2025 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号