Department of Biomedical Engineering, The Johns Hopkins University, 720 Rutland Ave., Baltimore, MD 21205, USA.
Prog Biophys Mol Biol. 2012 Oct-Nov;110(2-3):166-77. doi: 10.1016/j.pbiomolbio.2012.07.013. Epub 2012 Aug 7.
Since the first description of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs), these cells have garnered tremendous interest for their potential use in patient-specific analysis and therapy. Additionally, hiPSC-CMs can be derived from donor cells from patients with specific cardiac disorders, enabling in vitro human disease models for mechanistic study and therapeutic drug assessment. However, a full understanding of their electrophysiological and contractile function is necessary before this potential can be realized. Here, we review this emerging field from a functional perspective, with particular emphasis on beating rate, action potential, ionic currents, multicellular conduction, calcium handling and contraction. We further review extant hiPSC-CM disease models that recapitulate genetic myocardial disease.
自从首次描述人类诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)以来,这些细胞因其在患者特异性分析和治疗中的潜在用途而引起了极大的关注。此外,hiPSC-CMs 可以从患有特定心脏疾病的供体细胞中获得,从而可以建立体外人类疾病模型,用于机制研究和治疗药物评估。然而,在实现这一潜力之前,必须充分了解它们的电生理和收缩功能。在这里,我们从功能角度综述这一新兴领域,特别强调心率、动作电位、离子电流、细胞间传导、钙处理和收缩。我们进一步回顾了再现遗传心肌疾病的现有 hiPSC-CM 疾病模型。