From the McAllister Heart Institute, Department of Pathology and Laboratory Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill.
Circ Res. 2013 Sep 13;113(7):915-21. doi: 10.1161/CIRCRESAHA.112.300625.
Heart disease affects millions worldwide and is a progressive condition involving loss of cardiomyocytes. The human heart has limited endogenous regenerative capacity and is thus an important target for novel regenerative medicine approaches. Although cell-based regenerative therapies hold promise, cellular reprogramming of endogenous cardiac fibroblasts, which represent more than half of the cells in the mammalian heart, may be an attractive alternative strategy for regenerating cardiac muscle. Recent advances leveraging years of developmental biology point to the feasibility of generating de novo cardiomyocyte-like cells from terminally differentiated nonmyocytes in the heart in situ after ischemic damage. Here, we review the progress in cardiac reprogramming methods and consider the opportunities and challenges that lie ahead in refining this technology for regenerative medicine.
心脏病影响着全球数百万人,是一种涉及心肌细胞损失的进行性疾病。人类心脏的内源性再生能力有限,因此是新型再生医学方法的重要目标。尽管基于细胞的再生疗法具有广阔的前景,但对代表哺乳动物心脏中一半以上细胞的内源性心肌成纤维细胞进行细胞重编程,可能是一种有吸引力的替代策略,用于再生心肌。近年来,借助多年的发育生物学研究进展,人们发现,在缺血性损伤后,有可能从心脏中终末分化的非心肌细胞原位产生新的心肌细胞样细胞。在这里,我们回顾了心脏重编程方法的进展,并考虑了在为再生医学完善这项技术方面所面临的机遇和挑战。