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小细胞外囊泡介导的间充质干细胞抑制脑缺血再灌注损伤:系统评价和荟萃分析。

Inhibition of Cerebral Ischemia/Reperfusion Injury by MSCs-Derived Small Extracellular Vesicles in Rodent Models: A Systematic Review and Meta-Analysis.

机构信息

Department of Neurology, Affiliated Haikou Hospital of Xiangya School of Medicine, Central South University, Haikou 570208, China.

出版信息

Neural Plast. 2022 Oct 6;2022:3933252. doi: 10.1155/2022/3933252. eCollection 2022.

Abstract

Small extracellular vesicles (sEVs) secreted by mesenchymal stem cells (MSCs) have shown great therapeutic potential in cerebral ischemia-reperfusion injury (CIRI). In this study, we firstly performed a systematic review to evaluate the efficacy of MSCs-derived sEV for experimental cerebral ischemia/reperfusion injury. 24 studies were identified by searching 8 databases from January 2012 to August 2022. The methodological quality was assessed by using the SYRCLE 's risk of bias tool for animal studies. All the data were analyzed using RevMan 5.3 software. As a result, the score of study quality ranged from 3 to 9 in a total of ten points. Meta-analyses showed that MSCs-derived sEVs could effectively alleviate neurological impairment scores, reduced the volume of cerebral infarction and brain water content, and attenuated neuronal apoptosis. Additionally, the possible mechanisms of MSCs-derived sEVs for attenuating neuronal apoptosis were inhibiting microglia-mediated neuroinflammation. Thus, MSCs-derived sEVs might be regarded as a novel insight for cerebral ischemic stroke. However, further mechanistic studies, therapeutic safety, and clinical trials are required. Systematic review registration. PROSPERO CRD42022312227.

摘要

小细胞外囊泡 (sEVs) 由间充质干细胞 (MSCs) 分泌,在脑缺血再灌注损伤 (CIRI) 中显示出巨大的治疗潜力。在这项研究中,我们首先进行了一项系统评价,以评估 MSC 来源的 sEV 治疗实验性脑缺血再灌注损伤的疗效。通过从 2012 年 1 月至 2022 年 8 月搜索 8 个数据库,确定了 24 项研究。使用 SYRCLE 的动物研究偏倚风险工具评估方法学质量。使用 RevMan 5.3 软件对所有数据进行分析。结果,研究质量的评分在总共 10 分中从 3 分到 9 分不等。荟萃分析表明,MSC 来源的 sEV 可有效减轻神经功能缺损评分,减少脑梗死体积和脑含水量,减轻神经元凋亡。此外,MSC 来源的 sEV 减轻神经元凋亡的可能机制是抑制小胶质细胞介导的神经炎症。因此,MSC 来源的 sEV 可能为脑缺血性中风提供新的思路。然而,还需要进一步的机制研究、治疗安全性和临床试验。系统评价注册。PROSPERO CRD42022312227。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d501/9633211/1ac85278f2c6/NP2022-3933252.001.jpg

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