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采用细胞疗法恢复阿尔茨海默病小鼠模型中小胶质细胞 Trem2 功能。

A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer's disease.

机构信息

Institute for Stem Cell Biology and Regenerative Medicine and Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Institute for Stem Cell Biology and Regenerative Medicine and Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Cell Stem Cell. 2023 Aug 3;30(8):1043-1053.e6. doi: 10.1016/j.stem.2023.07.006.

Abstract

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.

摘要

阿尔茨海默病(AD)仍然是人类社会面临的重大挑战之一。这种普遍疾病的复杂和多方面的发病机制存在很多争议。然而,鉴于强有力的人类遗传证据,毫无疑问,小胶质细胞在预防神经元变性方面发挥着重要作用。例如,小胶质细胞基因 Trem2 的功能丧失会使小胶质细胞功能失调,并导致早发性神经退行性综合征,并且 Trem2 变体是 AD 最强的遗传风险因素之一。因此,恢复小胶质细胞功能代表了一种合理的治疗方法。在这里,我们表明,全身性造血细胞移植后增强小胶质细胞替代可恢复 AD 的 Trem2 突变小鼠模型中的小胶质细胞功能。

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