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巨噬细胞与中枢神经系统的髓鞘修复。

Macrophages and CNS remyelination.

机构信息

MRC Centre for Reproductive Health, The Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.

出版信息

J Neurochem. 2014 Jul;130(2):165-71. doi: 10.1111/jnc.12705. Epub 2014 Mar 26.

Abstract

Microglia are the resident macrophages of the central nervous system that survey the microenvironment for signals of injury or infection. The response to such signals induces an inflammatory response involving macrophages derived from both resident microglia and recruited circulating monocytes. Although implicated as contributors to autoimmune-mediated injury, microglia/ macrophages have recently been shown to be critical for the important central nervous system regenerative process of remyelination. This functional dichotomy may reflect their ability to be polarized along a continuum of activation states including the well-characterized cytotoxic M1 and regenerative M2 phenotypes. Here, we review the roles of microglia, monocytes and the macrophages which they give rise to in creating lesion environments favourable to remyelination, highlighting the specific roles of M1 and M2 phenotypes and how the pro-regenerative role of the innate immune system is altered by ageing. Here, we review the roles of microglia, monocytes and the macrophages, which they give rise to in creating lesion environments favourable to remyelination, highlighting the specific roles of activation phenotypes and how the pro-regenerative role of the innate immune system is altered by ageing.

摘要

小胶质细胞是中枢神经系统的常驻巨噬细胞,它们检测微环境中是否有损伤或感染的信号。对这些信号的反应会引发炎症反应,涉及来自常驻小胶质细胞和募集的循环单核细胞的巨噬细胞。尽管小胶质细胞/巨噬细胞被认为是自身免疫介导损伤的贡献者,但最近的研究表明,它们对中枢神经系统重要的髓鞘再生过程至关重要。这种功能上的二分法可能反映了它们能够沿着激活状态的连续体极化,包括特征明确的细胞毒性 M1 和再生性 M2 表型。在这里,我们回顾了小胶质细胞、单核细胞以及它们衍生的巨噬细胞在创造有利于髓鞘再生的病变环境中的作用,强调了 M1 和 M2 表型的特定作用,以及先天免疫系统的促再生作用如何因衰老而改变。

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