Mesenchymal stem cells in the treatment of ischemic stroke: progress and possibilities.

IF 1.7 Q4 CELL BIOLOGY
Thorsten R Doeppner, Dirk M Hermann
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引用次数: 42

Abstract

Stroke is a major cause of death and long-term disability in industrialized countries, and the only causal therapy for stroke comprises recombinant tissue plasminogen activator(rt-PA)-mediated recanalization of the occluded vessel. New experimental strategies focus on neuroregenerative approaches, among which the application of mesenchymal stem cells (MSCs) has gained increasing attention. MSCs, like other stem cells, have the capacity of unlimited self-renewal giving rise to differentiated cells from various cell lineages. Bone marrow (BM)-derived MSCs are the most frequently used MSC type in experimental stroke studies. Application of BM-derived MSCs and, in some studies, transplantation of MSCs from other tissue sources resulted in an improved functional recovery in experimental animals, although stroke volumes were not always affected by MSC transplantation. The underlying precise mechanisms of this phenomenon remain elusive, although MSC transplantation is considered to affect many diverse events, eg, by modulating the inflammatory milieu, stimulating endogenous neurogenesis and angiogenesis, and reducing glial scar formation. On the contrary, neuronal differentiation and integration of transplanted MSCs do not seem to affect stroke outcome significantly. On the basis of these preclinical studies, first clinical trials confirmed improved functional recovery in patients who had received BM-derived MSCs systemically, although the number of patients enrolled in these studies was low and there were no adequate control groups. In this review, we describe some fundamental biological characteristics of MSCs and further review some preclinical experimental studies, with special emphasis on BM-derived MSCs. We also review clinical trials in which MSCs have been used and conclude with a short outlook on the application of MSCs in stroke research.

间充质干细胞治疗缺血性中风:进展和可能性。
在工业化国家,卒中是死亡和长期残疾的主要原因,卒中的唯一因果治疗包括重组组织纤溶酶原激活剂(rt-PA)介导的闭塞血管再通。新的实验策略集中在神经再生方法,其中间充质干细胞(MSCs)的应用越来越受到关注。与其他干细胞一样,间充质干细胞具有无限自我更新的能力,可以从各种细胞系中分化成不同的细胞。骨髓(BM)来源的间充质干细胞是实验性卒中研究中最常用的间充质干细胞类型。尽管骨髓间充质干细胞移植并不总是影响脑卒中容量,但在一些研究中,应用脑梗死来源的间充质干细胞和移植其他组织来源的间充质干细胞可以改善实验动物的功能恢复。尽管MSC移植被认为影响许多不同的事件,例如,通过调节炎症环境,刺激内源性神经发生和血管生成,减少胶质瘢痕形成,但这种现象的潜在精确机制仍然难以捉摸。相反,移植间充质干细胞的神经元分化和整合似乎并不显著影响脑卒中的预后。在这些临床前研究的基础上,第一批临床试验证实,系统接受脑转移源性间充质干细胞的患者功能恢复得到改善,尽管纳入这些研究的患者数量较少,而且没有足够的对照组。在这篇综述中,我们描述了MSCs的一些基本生物学特性,并进一步回顾了一些临床前实验研究,特别强调了bm来源的MSCs。我们还回顾了MSCs在脑卒中研究中应用的临床试验,并对MSCs在脑卒中研究中的应用进行了简要展望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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