CHIT1调节阿尔茨海默病小胶质细胞的神经炎症和吞噬,抑制Aβ斑块沉积。

IF 5.6 2区 医学 Q1 ONCOLOGY
Shiyun Yuan, Fuxin Zhong, Tianchi Wan, Zhangjin Qin, Lihua Chen, Dianxia Xing, Wenbo Zhang, Wuhan Yu, Lihong Huang, Jiaqi Song, Weihua Yu, Yang Lü
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引用次数: 0

摘要

几丁质酶1 (CHIT1)作为一种几丁质特异性水解酶,通过小胶质细胞相关炎症和β淀粉样蛋白(a β)斑块积累显著影响阿尔茨海默病(AD)的进展。然而,CHIT1在AD中的确切作用机制尚不清楚。研究CHIT1对APP/PS1小鼠脑血流量(CBF)、海马体积和认知功能的影响。利用四维(4D)无标签定量(LFQ)蛋白质光谱分析CHIT1过表达引起的蛋白质改变。此外,利用膜片钳测量评估CHIT1对小胶质细胞电生理的影响,并利用N9、BV-2和HT-22细胞系检测其在ad样条件下对神经炎症、吞噬、小胶质细胞迁移和神经元凋亡的影响。CHIT1改善了APP/PS1小鼠的海马萎缩、脑灌流不足和认知功能缺陷。CHIT1通过其在AD中的相互作用调节小胶质细胞功能和神经元保护。CHIT1/IDH1水平的增加通过Ca2+激活的K+通道促进小胶质细胞的抗炎表型,增强小胶质细胞吞噬,促进Aβ清除。相反,敲低IDH1可减少抗炎药的分泌,增加炎症因子的产生,降低吞噬因子的表达,抑制Aβ内吞作用。此外,CHIT1通过减少凋亡因子的表达来减少神经元凋亡。然而,IDH1的敲除消除了CHIT1对神经元的保护作用。CHIT1通过与IDH1的相互作用在AD发病机制中发挥保护作用。CHIT1/IDH1通路通过小胶质细胞向抗炎状态的转变促进a β清除,并防止由a β毒性引起的神经元凋亡和功能障碍。©2025英国和爱尔兰病理学会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CHIT1 regulates the neuroinflammation and phagocytosis of microglia and suppresses Aβ plaque deposition in Alzheimer's disease.

Chitinase 1 (CHIT1), as a chitin-specific hydrolase, significantly influences the progression of Alzheimer's disease (AD) through microglia-associated inflammation and amyloid beta (Aβ) plaque accumulation. However, the precise mechanism of CHIT1 action in AD remains uncertain. The effects of CHIT1 on cerebral blood flow (CBF), hippocampal volume, and cognitive function were investigated in APP/PS1 mice. Protein alterations resulting from CHIT1 overexpression were analyzed using four-dimensional (4D) label-free quantitative (LFQ) protein spectrometry. Additionally, the influence of CHIT1 on microglial electrophysiology was assessed using patch clamp measurements, and its effects on neuroinflammation, phagocytosis, microglia migration, and neuronal apoptosis under AD-like conditions were examined using the cell lines N9, BV-2, and HT-22. CHIT1 ameliorated hippocampal atrophy, hypoperfusion, and cognitive function deficits in the APP/PS1 mouse. CHIT1 regulates microglial function and neuronal protection through its interactions in AD. Increased levels of CHIT1/IDH1 contributed to an anti-inflammatory phenotype in microglia via the Ca2+-activated K+ channel, enhanced microglial phagocytosis, and promoted Aβ clearance. Conversely, knocking down IDH1 reduced the secretion of anti-inflammatory agents and increased the production of inflammatory factors, as well as diminishing the expression of phagocytic factors and inhibiting Aβ endocytosis. Moreover, CHIT1 reduced neuronal apoptosis by diminishing the expression of apoptotic factors. However, IDH1 knockdown abrogated the protective effect of CHIT1 on neurons. CHIT1 exerts a protective role in AD pathogenesis through its interaction with IDH1. The CHIT1/IDH1 pathway promotes Aβ clearance via a shift in microglia toward an anti-inflammatory state and prevents neuronal apoptosis and dysfunction caused by Aβ toxicity. © 2025 The Pathological Society of Great Britain and Ireland.

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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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