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实质边界巨噬细胞调节 tau 病理和 tau 介导的神经退行性变。

Parenchymal border macrophages regulate tau pathology and tau-mediated neurodegeneration.

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.

Center for Brain Immunology and Glia, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Life Sci Alliance. 2023 Aug 10;6(11). doi: 10.26508/lsa.202302087. Print 2023 Nov.

Abstract

Parenchymal border macrophages (PBMs) reside close to the central nervous system parenchyma and regulate CSF flow dynamics. We recently demonstrated that PBMs provide a clearance pathway for amyloid-β peptide, which accumulates in the brain in Alzheimer's disease (AD). Given the emerging role for PBMs in AD, we explored how tau pathology affects the CSF flow and the PBM populations in the PS19 mouse model of tau pathology. We demonstrated a reduction of CSF flow, and an increase in an MHCIIPBM subpopulation in PS19 mice compared with WT littermates. Consequently, we asked whether PBM dysfunction could exacerbate tau pathology and tau-mediated neurodegeneration. Pharmacological depletion of PBMs in PS19 mice led to an increase in tau pathology and tau-dependent neurodegeneration, which was independent of gliosis or aquaporin-4 depolarization, essential for the CSF-ISF exchange. Together, our results identify PBMs as novel cellular regulators of tau pathology and tau-mediated neurodegeneration.

摘要

实质边界巨噬细胞(PBMs)位于靠近中枢神经系统实质的位置,调节脑脊液流动动力学。我们最近的研究表明,PBMs 为淀粉样β肽(Aβ)提供了清除途径,Aβ在阿尔茨海默病(AD)患者的大脑中积累。鉴于 PBMs 在 AD 中的作用不断显现,我们探讨了tau 病理学如何影响 PS19 小鼠模型中 CSF 流动和 PBM 群体。我们发现与 WT 同窝仔鼠相比,PS19 小鼠的 CSF 流动减少,且 MHCIIPBM 亚群增加。因此,我们想知道 PBM 功能障碍是否会加剧 tau 病理学和 tau 介导的神经退行性变。PS19 小鼠中 PBM 的药物耗竭导致 tau 病理学和 tau 依赖的神经退行性变增加,这与神经胶质增生或水通道蛋白-4 去极化无关,而水通道蛋白-4 去极化是 CSF-ISF 交换的必要条件。总的来说,我们的研究结果确定 PBMs 是 tau 病理学和 tau 介导的神经退行性变的新型细胞调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def3/10415611/c0f5f86f824d/LSA-2023-02087_Fig1.jpg

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