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间充质干细胞及其衍生的细胞外囊泡在急性心肌梗死后促进血管生成中的重要作用

The Vital Roles of Mesenchymal Stem Cells and the Derived Extracellular Vesicles in Promoting Angiogenesis After Acute Myocardial Infarction.

作者信息

Zhang Li-Li, Xiong Yu-Yan, Yang Yue-Jin

机构信息

State Key Laboratory of Cardiovascular Disease, Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

出版信息

Stem Cells Dev. 2021 Jun 1;30(11):561-577. doi: 10.1089/scd.2021.0006. Epub 2021 Apr 30.

Abstract

Acute myocardial infarction (AMI) is an event of ischemic myocardial necrosis caused by acute coronary artery occlusion, which ultimately leads to a large loss of cardiomyocytes. The prerequisite of salvaging ischemic myocardium and improving cardiac function of patients is to provide adequate blood perfusion in the infarcted area. Apart from reperfusion therapy, it is also urgent and imperative to promote angiogenesis. Recently, growing evidence based on promising preclinical data indicates that mesenchymal stem cells (MSCs) can provide therapeutic effects on AMI by promoting angiogenesis. Extracellular vesicles (EVs), membrane-encapsulated vesicles with complex cargoes, including proteins, nucleic acids, and lipids, can be derived from MSCs and represent part of their functions, so EVs also possess the ability to promote angiogenesis. However, poor control of the survival and localization of MSCs hindered clinical transformation and made scientists start looking for new approaches based on MSCs. Identifying the role of MSCs and their derived EVs in promoting angiogenesis can provide a theoretical basis for improved MSC-based methods, and ultimately promote the clinical treatment of AMI. This review highlights potential proangiogenic mechanisms of transplanted MSCs and the derived EVs after AMI and summarizes the latest literature concerning the novel methods based on MSCs to maximize the angiogenesis capability.

摘要

急性心肌梗死(AMI)是由急性冠状动脉闭塞引起的缺血性心肌坏死事件,最终导致大量心肌细胞丧失。挽救缺血心肌并改善患者心脏功能的前提是在梗死区域提供充足的血液灌注。除了再灌注治疗外,促进血管生成也迫在眉睫。最近,基于有前景的临床前数据的越来越多的证据表明,间充质干细胞(MSCs)可通过促进血管生成对AMI产生治疗作用。细胞外囊泡(EVs)是具有复杂货物(包括蛋白质、核酸和脂质)的膜包裹囊泡,可源自MSCs并代表其部分功能,因此EVs也具有促进血管生成的能力。然而,对MSCs存活和定位的控制不佳阻碍了临床转化,促使科学家开始寻找基于MSCs的新方法。确定MSCs及其衍生的EVs在促进血管生成中的作用可为改进基于MSCs的方法提供理论基础,并最终促进AMI的临床治疗。本综述重点介绍了AMI后移植的MSCs及其衍生的EVs的潜在促血管生成机制,并总结了有关基于MSCs的新方法以最大限度提高血管生成能力的最新文献。

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