National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
J Cell Mol Med. 2012 Aug;16(8):1663-8. doi: 10.1111/j.1582-4934.2012.01528.x.
Due to the extremely limited proliferative capacity of adult cardiomyocytes, human embryonic (pluripotent) stem cell derived cardiomyocytes (hESC-CMs) are currently almost the only reliable source of human heart cells which are suited to large-scale production. These cells have the potential for wide-scale application in drug discovery, heart disease research and cell-based heart repair. Embryonic atrial-, ventricular- and nodal-like cardiomyocytes can be obtained from differentiated human embryonic stem cells (hESCs). In recent years, several highly efficient cardiac differentiation protocols have been developed. Significant progress has also been made on understanding cardiac subtype specification, which is the key to reducing the heterogeneity of hESC-CMs, a major obstacle to the utilization of these cells in medical research and future cell-based replacement therapies. Herein we review recent progress in cardiac differentiation of hESCs and cardiac subtype specification, and discuss potential applications in drug screening and cell-based heart regeneration.
由于成人心肌细胞的增殖能力极其有限,人类胚胎(多能)干细胞衍生的心肌细胞(hESC-CMs)几乎是目前唯一适合大规模生产的可靠的人类心脏细胞来源。这些细胞在药物发现、心脏病研究和基于细胞的心脏修复方面具有广泛的应用潜力。可从分化的人类胚胎干细胞(hESCs)中获得胚胎心房、心室和神经节样心肌细胞。近年来,已经开发出几种高效的心脏分化方案。在理解心脏亚型特化方面也取得了重大进展,这是减少 hESC-CMs 异质性的关键,hESC-CMs 异质性是将这些细胞应用于医学研究和未来基于细胞的替代疗法的主要障碍。本文综述了 hESC 心脏分化和心脏亚型特化的最新进展,并讨论了其在药物筛选和基于细胞的心脏再生方面的潜在应用。