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嘌呤能受体 P2Y12 介导小胶质细胞内 tau 内吞。

Purinergic Receptor P2Y12-Mediated Tau Internalization in Microglia.

机构信息

Neurobiology Group, Division of Biochemical Sciences, CSIR-National Chemical Laboratory, Pune, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.

出版信息

Methods Mol Biol. 2024;2754:457-470. doi: 10.1007/978-1-0716-3629-9_25.

Abstract

Microglia are the resident brain macrophage cells that are involved in constant surveillance of brain microenvironment. In Alzheimer's disease, microglia get over activated upon the accumulation of Tau and amyloid-β species in the extracellular space, ultimately leading to neurodegeneration. Microglia phagocytose the extracellular Tau species by several mechanisms among which P2Y12 receptor-mediated internalization of extracellular Tau is recently studied. Extracellular Tau activates microglia and directly interacts with the P2Y12 receptor. Tau-receptor complex is then internalized followed by perinuclear accumulation and lysosomal degradation. Upon microglial activation by extracellular Tau, P2Y12 receptor is also involved in membrane-associated actin remodeling which has its key role in active migration and phagocytosis.

摘要

小胶质细胞是驻留于大脑中的巨噬细胞,参与大脑微环境的持续监测。在阿尔茨海默病中,小胶质细胞在外周空间中 Tau 和淀粉样-β物质的积累下过度激活,最终导致神经退行性变。小胶质细胞通过几种机制吞噬细胞外 Tau 物质,其中最近研究了 P2Y12 受体介导的细胞外 Tau 的内化。细胞外 Tau 激活小胶质细胞并直接与 P2Y12 受体相互作用。然后,Tau-受体复合物被内化,随后在核周积累和溶酶体降解。在细胞外 Tau 激活小胶质细胞后,P2Y12 受体也参与与膜相关的肌动蛋白重塑,其在活性迁移和吞噬作用中起关键作用。

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