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Cardiac progenitor reprogramming for heart regeneration

机译:心脏祖细胞重编程以实现心脏再生

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Myocardial infarction leads to the loss of a huge number of cardiomyocytes and the reparatory response to this phenomenon is scar tissue formation, which impairs heart function. Direct reprogramming technology offers an alternative strategy for the generation of functional cardiomyocytes not only in?vitro , but also in?vivo in the site of injury. Results have demonstrated cardiac tissue regeneration and improvement in heart function after myocardial infarction following local injection of vectors encoding reprogramming transcription factors or miRNAs. This shows the great potential of cardiac reprogramming technology for heart regeneration. However, in addition to cardiomyocytes, other cell types, including endothelial cells and smooth muscle cells are also required to be generated in the damaged area in order to achieve complete cardiac tissue regeneration. To this aim induced proliferative/expandable cardiovascular progenitor cells (iCPCs) appear to be an appropriate cell source, which is capable of differentiation into three cardiovascular lineages both in?vitro and in?vivo . In this regard, this study goes over in?vitro and in?vivo cardiac reprogramming technology and specifically deals with cardiac progenitor reprogramming and its potential for heart regeneration.
机译:心肌梗塞导致大量心肌细胞的丢失,对此现象的修复反应是形成疤痕组织,从而损害心脏功能。直接重编程技术不仅在体外,而且在受伤部位的体内提供功能性心肌细胞生成的替代策略。结果表明,局部注射编码重编程转录因子或miRNA的载体后,心肌梗塞后心脏组织再生并改善了心脏功能。这显示了心脏重编程技术对心脏再生的巨大潜力。然而,除了心肌细胞,还需要在受损区域中产生包括内皮细胞和平滑肌细胞在内的其他细胞类型,以实现完全的心脏组织再生。为了这个目的,诱导的增生/可扩张的心血管祖细胞(iCPCs)似乎是合适的细胞来源,其能够在体外和体内分化为三种心血管谱系。在这方面,这项研究超越了体外和体内心脏重编程技术,特别涉及心脏祖细胞重编程及其对心脏再生的潜力。

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