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间充质干细胞治疗缺血性中风的研究进展

Progress in Mesenchymal Stem Cell Therapy for Ischemic Stroke.

作者信息

Guo Yinghan, Peng Yucong, Zeng Hanhai, Chen Gao

机构信息

Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

出版信息

Stem Cells Int. 2021 Jun 15;2021:9923566. doi: 10.1155/2021/9923566. eCollection 2021.

Abstract

Ischemic stroke (IS) is a serious cerebrovascular disease with high morbidity and disability worldwide. Despite the great efforts that have been made, the prognosis of patients with IS remains unsatisfactory. Notably, recent studies indicated that mesenchymal stem cell (MSCs) therapy is becoming a novel research hotspot with large potential in treating multiple human diseases including IS. The current article is aimed at reviewing the progress of MSC treatment on IS. The mechanism of MSCs in the treatment of IS involved with immune regulation, neuroprotection, angiogenesis, and neural circuit reconstruction. In addition, nutritional cytokines, mitochondria, and extracellular vesicles (EVs) may be the main mediators of the therapeutic effect of MSCs. Transplantation of MSCs-derived EVs (MSCs-EVs) affords a better neuroprotective against IS when compared with transplantation of MSCs alone. MSC therapy can prolong the treatment time window of ischemic stroke, and early administration within 7 days after stroke may be the best treatment opportunity. The deliver routine consists of intraventricular, intravascular, intranasal, and intraperitoneal. Furthermore, several methods such as hypoxic preconditioning and gene technology could increase the homing and survival ability of MSCs after transplantation. In addition, MSCs combined with some drugs or physical therapy measures also show better neurological improvement. These data supported the notion that MSC therapy might be a promising therapeutic strategy for IS. And the application of new technology will promote MSC therapy of IS.

摘要

缺血性中风(IS)是一种严重的脑血管疾病,在全球范围内发病率和致残率都很高。尽管已经付出了巨大努力,但IS患者的预后仍然不尽人意。值得注意的是,最近的研究表明,间充质干细胞(MSCs)治疗正成为一个新的研究热点,在治疗包括IS在内的多种人类疾病方面具有巨大潜力。本文旨在综述MSCs治疗IS的研究进展。MSCs治疗IS的机制涉及免疫调节、神经保护、血管生成和神经回路重建。此外,营养细胞因子、线粒体和细胞外囊泡(EVs)可能是MSCs治疗作用的主要介质。与单独移植MSCs相比,移植MSCs来源的EVs(MSCs-EVs)对IS具有更好的神经保护作用。MSCs治疗可以延长缺血性中风的治疗时间窗,中风后7天内早期给药可能是最佳治疗时机。给药途径包括脑室内、血管内、鼻内和腹腔内。此外,低氧预处理和基因技术等几种方法可以提高MSCs移植后的归巢和存活能力。此外,MSCs与一些药物或物理治疗措施联合应用也显示出更好的神经功能改善。这些数据支持了MSCs治疗可能是IS一种有前景的治疗策略的观点。新技术的应用将促进IS的MSCs治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87e1/8219421/7e1e0c79b7e9/SCI2021-9923566.001.jpg

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