Freund Christian, Mummery Christine L
Department of Anatomy & Embryology, Leiden University Medical Center, The Netherlands.
J Cell Biochem. 2009 Jul 1;107(4):592-9. doi: 10.1002/jcb.22164.
The derivation of embryonic stem cells (hESC) from human embryos a decade ago started a new era in perspectives for cell therapy as well as understanding human development and disease. More recently, reprogramming of somatic cells to an embryonic stem cell-like state (induced pluripotent stem cells, iPS) presented a new milestone in this area, making it possible to derive all cells types from any patients bearing specific genetic mutations. With the development of efficient differentiation protocols we are now able to use the derivatives of pluripotent stem cells to study mechanisms of disease and as human models for drug and toxicology testing. In addition derivatives of pluripotent stem cells are now close to be used in clinical practice although for the heart, specific additional challenges have been identified that preclude short-term application in cell therapy. Here we review techniques presently used to induce differentiation of pluripotent stem cells into cardiomyocytes and the potential these cells have as disease models and for therapy.
十年前从人类胚胎中获得胚胎干细胞开启了细胞治疗以及理解人类发育与疾病领域的新纪元。最近,将体细胞重编程为胚胎干细胞样状态(诱导多能干细胞,iPS)成为该领域的一个新里程碑,使得从任何携带特定基因突变的患者身上获得所有细胞类型成为可能。随着高效分化方案的发展,我们现在能够利用多能干细胞的衍生物来研究疾病机制,并将其作为药物和毒理学测试的人体模型。此外,多能干细胞的衍生物目前已接近应用于临床实践,尽管对于心脏疾病,已发现一些特殊的额外挑战,这使得其在细胞治疗中的短期应用受到限制。在此,我们综述目前用于诱导多能干细胞分化为心肌细胞的技术,以及这些细胞作为疾病模型和用于治疗的潜力。