Cellular Dynamics International, Inc, 525 Science Drive, Madison, WI 53711, USA.
J Cardiovasc Transl Res. 2011 Feb;4(1):66-72. doi: 10.1007/s12265-010-9235-1.
Moving from the bench to the bedside is an expensive and arduous journey with a high risk of failure. One roadblock on the path of translational medicine is the paucity of predictive in vitro models available during preclinical drug development. The ability of human embryonic stem (ES) and induced pluripotent stem (iPS) cells to generate virtually any tissue of the body, in vitro, makes these cells an obvious choice for use in drug discovery and translational medicine. Technological advancements in the production of stem cells and their differentiation into relevant cell types, such as cardiomyocytes, has permitted the utility of these cells in the translational medicine setting. In particular, the derivation and differentiation of patient-specific iPS cells will facilitate an understanding of basic disease etiology, enable better drug efficacy and safety screens, and ultimately lead to personalized patient therapies. This review will focus on recent advancements in the derivation and differentiation of human ES and iPS cells into cardiomyocytes and their uses in safety testing and modeling human disease.
从实验室走向临床是一条代价高昂且艰巨的道路,失败的风险很高。转化医学道路上的一个障碍是在临床前药物开发期间可用的预测性体外模型稀缺。人类胚胎干细胞 (ES) 和诱导多能干细胞 (iPS) 细胞在体外生成几乎任何身体组织的能力,使这些细胞成为药物发现和转化医学中应用的明显选择。干细胞生产技术的进步及其分化为相关细胞类型(如心肌细胞),使得这些细胞在转化医学环境中得到了应用。特别是,患者特异性 iPS 细胞的衍生和分化将有助于理解基本疾病病因,能够进行更好的药物疗效和安全性筛选,并最终导致个性化的患者治疗。本文将重点介绍人类 ES 和 iPS 细胞向心肌细胞的衍生和分化的最新进展,及其在安全性测试和模拟人类疾病方面的应用。