Department of Medicine, University of Minnesota Medical School , Minneapolis, Minnesota 55455, USA.
Antioxid Redox Signal. 2010 Dec 15;13(12):1879-97. doi: 10.1089/ars.2010.3434. Epub 2010 Oct 28.
Stem cell transplantation has emerged as a novel treatment option for ischemic heart disease. Different cell types have been utilized and the recent development of induced pluripotent stem cells has generated tremendous excitement in the regenerative field. Bone marrow-derived multipotent progenitor cell transplantation in preclinical large animal models of postinfarction left ventricular remodeling has demonstrated long-term functional and bioenergetic improvement. These beneficial effects are observed despite no significant engraftment of bone marrow cells in the myocardium and even lower differentiation of these cells into cardiomyocytes. It is thought to be related to the paracrine effect of these stem cells, which secrete factors that lead to long-term gene expression changes in the host myocardium, thereby promoting neovascularization, inhibiting apoptosis, and stimulating resident cardiac progenitor cells. Future studies are warranted to examine the changes in the recipient myocardium after stem cell transplantation and to investigate the signaling pathways involved in these effects.
干细胞移植已成为缺血性心脏病的一种新的治疗选择。不同的细胞类型已被应用,而诱导多能干细胞的最新发展在再生领域引起了极大的兴奋。骨髓来源的多能祖细胞移植在梗死后左心室重构的临床前大型动物模型中已证明具有长期的功能和生物能量改善。尽管骨髓细胞在心肌中的植入没有明显增加,甚至这些细胞向心肌细胞的分化更低,但仍观察到这些有益的效果。这被认为与这些干细胞的旁分泌作用有关,它们分泌的因子导致宿主心肌的长期基因表达变化,从而促进血管生成、抑制细胞凋亡,并刺激驻留的心脏祖细胞。有必要进行未来的研究来检查干细胞移植后受体心肌的变化,并研究涉及这些效应的信号通路。