Suppr超能文献

[阿尔茨海默病中含pyrin结构域的核苷酸结合寡聚化结构域样受体家族3炎性小体]

[Nucleotide-binding Oligomerization Domain-like Receptor Family Pyrin Domain Containing 3 Inflammasome in Alzheimer's Disease].

作者信息

Feng Yun-Ying, Chen Hui

机构信息

School of Basic Medicine,CAMS and PUMC,Beijing 100730,China.

Department of Immunology,Institute of Basic Medical Sciences,CAMS and PUMC,Beijing 100005,China.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2021 Oct;43(5):788-795. doi: 10.3881/j.issn.1000-503X.12585.

Abstract

Alzheimer's disease(AD)is a chronic neurodegenerative disease whose cause remains unclear.The β-amyloid plaques in the brain are one of the major pathological features of AD.However,the drugs targeting extracellular β-amyloid plaques have failed to cure the disease.Innate immunity and neuroinflammation play a role in the pathogenesis and progression of AD.As the macrophages existing in the central nervous system,microglia are related with extracellular β-amyloid deposition,intracellular neurofibrillary tangle formation,and neuron injury.Accumulating evidence demonstrates that the activation of nucleotide-binding oligomerization domain-like receptor family pyrin domain containing 3(NLRP3)inflammasome in microglia plays a role in AD,suggesting new therapeutic target for AD in this signaling pathway.This article reviewed the studies about the activation and regulation of NLRP3 inflammasome in the pathogenesis and progression of AD as well as the development of AD therapies targeting this pathway,aiming to provide reference for further studies in this field.

摘要

阿尔茨海默病(AD)是一种病因不明的慢性神经退行性疾病。大脑中的β-淀粉样蛋白斑块是AD的主要病理特征之一。然而,针对细胞外β-淀粉样蛋白斑块的药物未能治愈该疾病。固有免疫和神经炎症在AD的发病机制和进展中起作用。作为存在于中枢神经系统中的巨噬细胞,小胶质细胞与细胞外β-淀粉样蛋白沉积、细胞内神经原纤维缠结形成以及神经元损伤有关。越来越多的证据表明,小胶质细胞中含pyrin结构域的核苷酸结合寡聚化结构域样受体家族3(NLRP3)炎性小体的激活在AD中起作用,提示该信号通路是AD的新治疗靶点。本文综述了关于NLRP3炎性小体在AD发病机制和进展中的激活与调节以及针对该通路的AD治疗进展的研究,旨在为该领域的进一步研究提供参考。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验