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Excitation–contraction coupling of human induced pluripotent stem cell-derived cardiomyocytes

机译:人诱导的多能干细胞来源的心肌细胞的兴奋-收缩偶联

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摘要

Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) hold enormous potential in many fields of cardiovascular research. Overcoming many of the limitations of their embryonic counterparts, the application of iPSC-CMs ranges from facilitating investigation of familial cardiac disease and pharmacological toxicity screening to personalized medicine and autologous cardiac cell therapies. The main factor preventing the full realization of this potential is the limited maturity of iPSC-CMs, which display a number of substantial differences in comparison to adult cardiomyocytes. Excitation–contraction (EC) coupling, a fundamental property of cardiomyocytes, is often described in iPSC-CMs as being more analogous to neonatal than adult cardiomyocytes. With Ca2+ handling linked, directly or indirectly, to almost all other properties of cardiomyocytes, a solid understanding of this process will be crucial to fully realizing the potential of this technology. Here, we discuss the implications of differences in EC coupling when considering the potential applications of human iPSC-CMs in a number of areas as well as detailing the current understanding of this fundamental process in these cells.
机译:诱导多能干细胞衍生的心肌细胞(iPSC-CM)在心血管研究的许多领域中具有巨大的潜力。克服其胚胎对应物的许多限制,iPSC-CM的应用范围从促进家族性心脏病的研究和药理毒性筛选到个性化药物和自体心脏细胞疗法。阻止充分发挥这种潜力的主要因素是iPSC-CM的成熟度有限,与成年心肌细胞相比,iPSC-CM表现出许多实质性差异。激励-收缩(EC)耦合是心肌细胞的基本属性,在iPSC-CM中通常将其描述为比成人心肌细胞更类似于新生儿。通过将Ca 2 + 处理直接或间接与心肌细胞的几乎所有其他属性联系起来,对这一过程的扎实了解对于充分实现该技术的潜力至关重要。在这里,我们讨论在考虑人类iPSC-CM在许多领域的潜在应用时,EC耦合差异的含义,并详细介绍当前对这些细胞中基本过程的理解。

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