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基因编辑间充质干细胞及其在急性心血管疾病中的临床应用潜力

Genetically modified mesenchymal stem cells and their clinical potential in acute cardiovascular disease.

作者信息

Griffin Matthew, Greiser Udo, Barry Frank, O'Brien Timothy, Ritter Thomas

机构信息

College of Medicine, Nursing and Health Sciences and Regenerative Medicine Institute, National Centre for Biomedical Engineering Science, National University of Ireland, Galway, Ireland.

出版信息

Discov Med. 2010 Mar;9(46):219-23.

Abstract

Adult mesenchymal stem cells (MSCs) are non-hematopoietic cells with multi-lineage potential to differentiate into various tissues of mesodermal origin. They can be isolated from bone marrow and other tissues and have the capacity to extensively proliferate in vitro. Moreover, MSCs have also been shown to produce anti-inflammatory molecules which can modulate humoral and cellular immune responses. Considering their regenerative potential and immunoregulatory effect, MSC therapy is a promising tool in the treatment of degenerative, inflammatory, and autoimmune diseases. However, the current understanding from results of clinical trials is that MSC-therapy is safe but its therapeutic efficiency needs to be improved. In this article we will focus on options for genetic manipulation of MSCs and on current progress in adapting genetically-modified MSCs for clinical use in acute cardiovascular disease.

摘要

成人间充质干细胞(MSCs)是一种非造血细胞,具有多向分化潜能,可分化为各种中胚层来源的组织。它们可以从骨髓和其他组织中分离出来,并具有在体外大量增殖的能力。此外,MSCs还被证明能产生抗炎分子,可调节体液免疫和细胞免疫反应。鉴于其再生潜能和免疫调节作用,MSCs疗法是治疗退行性、炎症性和自身免疫性疾病的一种有前景的工具。然而,目前从临床试验结果中得到的认识是,MSCs疗法是安全的,但其治疗效果有待提高。在本文中,我们将重点关注MSCs的基因操作方法,以及在使基因修饰的MSCs适应急性心血管疾病临床应用方面的当前进展。

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