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急性缺血性卒中中神经元与小胶质细胞相互作用模式的时空图谱

Spatial and temporal mapping of neuron-microglia interaction modes in acute ischemic stroke.

作者信息

Dou Xiaoke, Ji Wei, Dai Maosha, Sun Shujun, Chen Rui, Yang Juexi, Long Junhao, Ge Yangyang, Lin Yun

机构信息

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Institute of Anesthesia and Critical Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China; Key Laboratory of Anesthesiology and Resuscitation (Huazhong University of Science and Technology), Ministry of Education, China.

Department of Anesthesiology, Yantai Affiliated Hospital of BinZhou Medical College, Yantai 264000, China.

出版信息

Biochem Pharmacol. 2023 Oct;216:115772. doi: 10.1016/j.bcp.2023.115772. Epub 2023 Sep 1.

Abstract

Ischemic stroke (IS) is a major cause of morbidity and mortality worldwide, accounting for 75-80% of all strokes. Under conditions of ischemia and hypoxia, neurons suffer damage or death, leading to a series of secondary immune reactions. Microglia, the earliest activated immune cells, can exert neurotoxic or neuroprotective effects on neurons through secretion of factors. There exists a complex interaction between neurons and microglia during this process. Moreover, the interaction between them becomes even more complex due to differences in the infarct area and reperfusion time. This review first elaborates on the differences in neuronal death modes between the ischemic core and penumbra, and then introduces the differences in microglial markers across different infarct areas with varying reperfusion time, indicating distinct functions. Finally, we focus on exploring the interaction modes between neurons and microglia in order to precisely target beneficial interactions and inhibit harmful ones, thus providing new therapeutic strategies for the treatment of IS.

摘要

缺血性中风(IS)是全球发病和死亡的主要原因,占所有中风的75-80%。在缺血缺氧条件下,神经元会遭受损伤或死亡,从而引发一系列继发性免疫反应。小胶质细胞是最早被激活的免疫细胞,可通过分泌因子对神经元产生神经毒性或神经保护作用。在此过程中,神经元和小胶质细胞之间存在复杂的相互作用。此外,由于梗死面积和再灌注时间的差异,它们之间的相互作用变得更加复杂。本文综述首先阐述了缺血核心区和半暗带神经元死亡模式的差异,然后介绍了不同梗死面积和不同再灌注时间下小胶质细胞标志物的差异,表明其功能不同。最后,我们着重探讨神经元和小胶质细胞之间的相互作用模式,以便精准靶向有益相互作用并抑制有害相互作用,从而为缺血性中风的治疗提供新的治疗策略。

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