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衰老相关神经行为和神经炎症性疾病中的小胶质细胞动力学。

Microglia dynamics in aging-related neurobehavioral and neuroinflammatory diseases.

机构信息

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.

USERN Office, Babol University of Medical Sciences, Babol, Iran.

出版信息

J Neuroinflammation. 2022 Nov 17;19(1):273. doi: 10.1186/s12974-022-02637-1.

Abstract

Microglia represent the first line of immune feedback in the brain. Beyond immune surveillance, they are essential for maintaining brain homeostasis. Recent research has revealed the microglial cells' spatiotemporal heterogeneity based on their local and time-based functions in brain trauma or disease when homeostasis is disrupted. Distinct "microglial signatures" have been recorded in physiological states and brain injuries, with discrete or sometimes overlapping pro- and anti-inflammatory functions. Microglia are involved in the neurological repair processes, such as neurovascular unit restoration and synaptic plasticity, and manage the extent of the damage due to their phenotype switching. The versatility of cellular phenotypes beyond the classical M1/M2 classification, as well as the double-edge actions of microglia in neurodegeneration, indicate the need for further exploration of microglial cell dynamics and their contribution to neurodegenerative processes. This review discusses the homeostatic functions of different microglial subsets focusing on neuropathological conditions. Also, we address the feasibility of targeting microglia as a therapeutic strategy in neurodegenerative diseases.

摘要

小胶质细胞代表了大脑中免疫反馈的第一道防线。除了免疫监视,它们对于维持大脑内环境稳态也是必不可少的。最近的研究揭示了小胶质细胞的时空异质性,基于它们在大脑创伤或疾病时的局部和时间依赖性功能,此时内环境稳态被打破。在生理状态和脑损伤中记录了不同的“小胶质细胞特征”,具有离散或有时重叠的促炎和抗炎功能。小胶质细胞参与神经修复过程,如神经血管单元的修复和突触可塑性,并通过表型转换来控制损伤的程度。除了经典的 M1/M2 分类之外,细胞表型的多功能性,以及小胶质细胞在神经退行性变中的双刃剑作用,表明需要进一步探索小胶质细胞的动力学及其对神经退行性过程的贡献。这篇综述讨论了不同小胶质细胞亚群的稳态功能,重点关注神经病理学状况。此外,我们还探讨了将小胶质细胞作为神经退行性疾病治疗策略的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/9670665/cf619a058d4f/12974_2022_2637_Fig1_HTML.jpg

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