Piccoli Marco, Cirillo Federica, Tettamanti Guido, Anastasia Luigi
Laboratory of Stem Cells for Tissue Engineering, IRCCS Policlinico San Donato, 20097 San Donato Milanese, Milan, Italy.
Department of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Eur Heart J Suppl. 2016 Apr 28;18(Suppl E):E1-E7. doi: 10.1093/eurheartj/suw018. Epub 2016 Apr 29.
The possibility of generating induced pluripotent stem cells from mouse embryonic fibroblasts and human adult fibroblasts has introduced new perspectives for possible therapeutic strategies to repair damaged hearts. However, obtaining large numbers of adult stem cells is still an ongoing challenge, and the safety of genetic reprogramming with lenti- or retro-viruses has several drawbacks not easy to be addressed. Furthermore, the majority of adult stem cell-based clinical trials for heart regeneration have had generally poor and controversial results. Nonetheless, it is now clear that the injected cells activate the growth and differentiation of progenitor cells that are already present in the heart. This is achieved by the release of signalling factors and/or exosomes carrying them. Along this line, chemistry may play a major role in developing new strategies for activating resident stem cells to regenerate the heart. In particular, this review focuses on small molecule approaches for cell reprogramming, cell differentiation, and activation of cell protection.
从小鼠胚胎成纤维细胞和人类成纤维细胞中生成诱导多能干细胞的可能性为修复受损心脏的潜在治疗策略带来了新的视角。然而,获取大量成体干细胞仍是一个持续存在的挑战,并且使用慢病毒或逆转录病毒进行基因重编程的安全性存在一些不易解决的缺点。此外,大多数基于成体干细胞的心脏再生临床试验结果普遍不佳且存在争议。尽管如此,现在已经明确注入的细胞会激活心脏中已存在的祖细胞的生长和分化。这是通过释放信号因子和/或携带这些因子的外泌体来实现的。沿着这条线,化学在开发激活驻留干细胞以再生心脏的新策略中可能发挥主要作用。特别是,本综述重点关注用于细胞重编程、细胞分化和激活细胞保护的小分子方法。