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P2Y12R 依赖性易位机制调控小胶质细胞景观变化。

P2Y12R-Dependent Translocation Mechanisms Gate the Changing Microglial Landscape.

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.

Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA; Department of Neurology, First Affiliated Hospital of Guangzhou Medical University, Guangdong 510120, China.

出版信息

Cell Rep. 2018 Apr 24;23(4):959-966. doi: 10.1016/j.celrep.2018.04.001.

Abstract

Microglia are an exquisitely tiled and self-contained population in the CNS that do not receive contributions from circulating monocytes in the periphery. While microglia are long-lived cells, the extent to which their cell bodies are fixed and the molecular mechanisms by which the microglial landscape is regulated have not been determined. Using chronic in vivo two-photon imaging to follow the microglial population in young adult mice, we document a daily rearrangement of the microglial landscape. Furthermore, we show that the microglial landscape can be modulated by severe seizures, acute injury, and sensory deprivation. Finally, we demonstrate a critical role for microglial P2Y12Rs in regulating the microglial landscape through cellular translocation independent of proliferation. These findings suggest that microglial patrol the CNS through both process motility and soma translocation.

摘要

小胶质细胞是中枢神经系统中一种排列精细且自给自足的细胞群体,它们不接受外周循环单核细胞的贡献。虽然小胶质细胞是长寿细胞,但它们的胞体固定程度以及调节小胶质细胞景观的分子机制尚未确定。我们使用慢性体内双光子成像来跟踪年轻成年小鼠中的小胶质细胞群体,记录了小胶质细胞景观的日常重新排列。此外,我们还表明,小胶质细胞景观可以通过严重的癫痫发作、急性损伤和感觉剥夺来调节。最后,我们证明了小胶质细胞 P2Y12R 通过与增殖无关的细胞内转位在调节小胶质细胞景观中起关键作用。这些发现表明,小胶质细胞通过突起运动和胞体转位来巡逻中枢神经系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d512/5965271/ea4b090eee76/nihms965673f1.jpg

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