Microglia drive APOE-dependent neurodegeneration in a tauopathy mouse model

Yang Shi, Melissa Manis, J. Long, Kairuo Wang, P. Sullivan, Javier Remolina Serrano, Rosa Hoyle, D. Holtzman
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引用次数: 218

Abstract

Shi et al. find that microglia, instead of tau-induced direct neurotoxicity, are the driving force of neurodegeneration in a tauopathy mouse model. Microglia are also required for tau pathogenesis. In addition, apoE strongly regulates neurodegeneration in the setting of tauopathy predominantly by modulating microglial function.
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小胶质细胞驱动apoe依赖性脑损伤小鼠模型的神经变性
Shi等人发现,在牛头病小鼠模型中,小胶质细胞而不是tau诱导的直接神经毒性是神经退行性变的驱动力。小胶质细胞也是tau发病所必需的。此外,apoE主要通过调节小胶质细胞功能,在牛头病的情况下强烈调节神经退行性变。
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