Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Nat Biomed Eng. 2018 Jun;2(6):392-398. doi: 10.1038/s41551-018-0244-8. Epub 2018 Jun 11.
Human pluripotent stem cells (hPSCs), in particular embryonic stem cells and induced pluripotent stem cells, have received enormous attention in cardiovascular regenerative medicine owing to their ability to expand and differentiate into functional cardiomyocytes and other cardiovascular cell types. Despite the potential applications of hPSCs for tissue regeneration in patients suffering from cardiovascular disease, whether hPSC-based therapies can be safe and efficacious remains inconclusive, with strong evidence from clinical trials lacking. Critical factors limiting therapeutic efficacy are the degree of maturity and purity of the hPSC-derived differentiated progeny, and the tumorigenic risk associated with residual undifferentiated cells. In this Review, we discuss recent advances in cardiac-cell differentiation from hPSCs and in the direct reprogramming of non-myocyte cells for cardiovascular regenerative applications. We also discuss approaches for the delivery of cells to diseased tissue, and how such advances are contributing to progress in cardiac tissue engineering for tackling heart disease.
人类多能干细胞(hPSCs),尤其是胚胎干细胞和诱导多能干细胞,由于其能够扩增并分化为功能性心肌细胞和其他心血管细胞类型,在心血管再生医学中受到了极大的关注。尽管 hPSCs 在治疗心血管疾病患者的组织再生方面具有潜在的应用前景,但 hPSC 疗法是否安全有效仍不确定,临床试验缺乏有力证据。限制治疗效果的关键因素是 hPSC 来源的分化后代的成熟度和纯度,以及与残留未分化细胞相关的致瘤风险。在这篇综述中,我们讨论了 hPSC 向心脏细胞分化以及非心肌细胞的直接重编程在心血管再生应用方面的最新进展。我们还讨论了将细胞递送到病变组织的方法,以及这些进展如何促进心脏组织工程在解决心脏病方面的进展。