特雷姆2
生物
小胶质细胞
疾病
功能(生物学)
移植
神经科学
遗传增强
损失函数
发病机制
人性化鼠标
基因
免疫学
病理
遗传学
免疫系统
炎症
表型
内科学
医学
作者
Yongjin Yoo,Gernot Neumayer,Yohei Shibuya,Marius Marc-Daniel Mader,Marius Wernig
出处
期刊:Cell Stem Cell
[Elsevier]
日期:2023-08-01
卷期号:30 (8): 1043-1053.e6
被引量:24
标识
DOI:10.1016/j.stem.2023.07.006
摘要
Summary
Alzheimer's disease (AD) remains one of the grand challenges facing human society. Much controversy exists around the complex and multifaceted pathogenesis of this prevalent disease. Given strong human genetic evidence, there is little doubt, however, that microglia play an important role in preventing degeneration of neurons. For example, loss of function of the microglial gene Trem2 renders microglia dysfunctional and causes an early-onset neurodegenerative syndrome, and Trem2 variants are among the strongest genetic risk factors for AD. Thus, restoring microglial function represents a rational therapeutic approach. Here, we show that systemic hematopoietic cell transplantation followed by enhancement of microglia replacement restores microglial function in a Trem2 mutant mouse model of AD.
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