Neurobiology Group, Division of Biochemical Sciences, CSIR-National Chemical Laboratory, Pune, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.
Methods Mol Biol. 2024;2754:457-470. doi: 10.1007/978-1-0716-3629-9_25.
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.
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。