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Maturation of Cardiomyocytes Derived from Human Pluripotent Stem Cells: Current Strategies and Limitations

机译:人多能干细胞衍生的心肌细胞的成熟:当前策略和局限性。

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摘要

The capacity of differentiation of human pluripotent stem cells (hPSCs), which include both embryonic stem cells and induced pluripotent stem cells, into cardiomyocytes (CMs) in vitro provides an unlimited resource for human CMs for a wide range of applications such as cell based cardiac repair, cardiac drug toxicology screening, and human cardiac disease modeling. However, their applicability is significantly limited by immature phenotypes. It has been well known that currently available CMs derived from hPSCs (hPSC-CMs) represent immature embryonic or fetal stage CMs and are functionally and structurally different from mature human CMs. To overcome this critical issue, several new approaches aiming to generate more mature hPSC-CMs have been developed. This review describes recent approaches to generate more mature hPSC-CMs including their scientific principles, advantages, and limitations.
机译:人多能干细胞(hPSC)的分化能力(包括胚胎干细胞和诱导性多能干细胞)在体外向心肌细胞(CM)分化的能力为人类CM提供了无限的资源,可用于多种应用,例如基于细胞的心脏维修,心脏药物毒理学筛查和人类心脏疾病建模。但是,它们的适用性受到未成熟表型的极大限制。众所周知,源自hPSC的当前可用CM(hPSC-CM)代表未成熟的胚胎或胎儿期CM,并且在功能和结构上与成熟的人CM不同。为了克服这个关键问题,已经开发了几种旨在产生更成熟的hPSC-CM的新方法。这篇综述描述了生成更成熟的hPSC-CM的最新方法,包括它们的科学原理,优点和局限性。

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