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Strategies and Challenges to Improve Cellular Programming-Based Approaches for Heart Regeneration Therapy

机译:改善基于细胞编程的心脏再生治疗方法的策略和挑战

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摘要

Limited adult cardiac cell proliferation after cardiovascular disease, such as heart failure, hampers regeneration, resulting in a major loss of cardiomyocytes (CMs) at the site of injury. Recent studies in cellular reprogramming approaches have provided the opportunity to improve upon previous techniques used to regenerate damaged heart. Using these approaches, new CMs can be regenerated from differentiation of iPSCs (similar to embryonic stem cells), the direct reprogramming of fibroblasts [induced cardiomyocytes (iCMs)], or induced cardiac progenitors. Although these CMs have been shown to functionally repair infarcted heart, advancements in technology are still in the early stages of development in research laboratories. In this review, reprogramming-based approaches for generating CMs are briefly introduced and reviewed, and the challenges (including low efficiency, functional maturity, and safety issues) that hinder further translation of these approaches into a clinical setting are discussed. The creative and combined optimal methods to address these challenges are also summarized, with optimism that further investigation into tissue engineering, cardiac development signaling, and epigenetic mechanisms will help to establish methods that improve cell-reprogramming approaches for heart regeneration.
机译:有限的成人心脏细胞增殖在心血管疾病之后,心力衰竭,妨碍再生,导致损伤部位的主要损失心肌细胞(CMS)。最近的细胞重编程方法的研究提供了改善以前用于再生受损心脏的技术的机会。使用这些方法,可以从IPSC的分化(类似于胚胎干细胞)来再生新的CMS,成纤维细胞的直接重新编程[诱导心肌细胞(ICMS),或诱导的心脏祖细胞。虽然这些CMS已被证明是在功能上修复令人心中的,但技术进步仍处于研究实验室的早期发展阶段。在本综述中,简要介绍和审查了基于重新编程的生成CMS方法,并审查了阻碍这些方法进一步翻译这些方法的挑战(包括低效率,功能成熟度和安全问题)。还概述了解决这些挑战的创造力和组合的最佳方法,乐观地,进一步调查组织工程,心脏发育信号和表观遗传机制将有助于建立改善细胞重新编程的心脏再生方法的方法。

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