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小胶质细胞本体论与信号转导

Microglia Ontology and Signaling.

机构信息

Neuroscience Laboratory, CHU de Québec Research Center (CHUL), Department of Psychiatry and Neuroscience, Faculty of Medicine, Laval University Quebec, CA, Canada.

Neuroscience Laboratory, CHU de Québec Research Center (CHUL), Department of Molecular Medicine, Faculty of Medicine, Laval University Quebec, CA, Canada.

出版信息

Front Cell Dev Biol. 2016 Jun 29;4:72. doi: 10.3389/fcell.2016.00072. eCollection 2016.

Abstract

Microglia constitute the powerhouse of the innate immune system in the brain. It is now widely accepted that they are monocytic-derived cells that infiltrate the developing brain at the early embryonic stages, and acquire a resting phenotype characterized by the presence of dense branching processes, called ramifications. Microglia use these dynamic ramifications as sentinels to sense and detect any occurring alteration in brain homeostasis. Once a danger signal is detected, such as molecular factors associated to brain damage or infection, they get activated by acquiring a less ramified phenotype, and mount adequate responses that range from phagocyting cell debris to secreting inflammatory and trophic factors. Here, we review the origin of microglia and we summarize the main molecular signals involved in controlling their function under physiological conditions. In addition, their implication in the pathogenesis of multiple sclerosis and stress is discussed.

摘要

小胶质细胞构成了大脑中先天免疫系统的主力军。现在人们普遍认为,它们是单核细胞衍生的细胞,在胚胎早期就渗透到发育中的大脑中,并获得了一种静止表型,其特征是存在密集分支的过程,称为树突。小胶质细胞利用这些动态的树突作为哨兵,感知和检测大脑内稳态发生的任何变化。一旦检测到危险信号,例如与脑损伤或感染相关的分子因素,它们就会通过获得较少分支的表型而被激活,并产生适当的反应,范围从吞噬细胞碎片到分泌炎症和营养因子。在这里,我们回顾了小胶质细胞的起源,并总结了控制其在生理条件下功能的主要分子信号。此外,还讨论了它们在多发性硬化症和应激发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c64/4925666/5369e1d1b0f2/fcell-04-00072-g0001.jpg

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