Production of De Novo Cardiomyocytes: Human Pluripotent Stem Cell Differentiation and Direct Reprogramming

被引:551
作者
Burridge, Paul W. [1 ,2 ]
Keller, Gordon [3 ]
Gold, Joseph D. [4 ]
Wu, Joseph C. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Cardiovasc Inst, Stanford, CA 94305 USA
[3] MaRS Ctr, Univ Hlth Network, McEwen Ctr Regenerat Med, Toronto, ON MG5 1L7, Canada
[4] Geron Corp, Neurobiol & Cell Therapies Res, Menlo Pk, CA 94025 USA
关键词
PROMOTES CARDIAC DIFFERENTIATION; FUNCTIONAL-PROPERTIES; HEART REGENERATION; MOUSE FIBROBLASTS; MASTER REGULATOR; SMOOTH-MUSCLE; PROLIFERATION; MESODERM; MESP1; PROGENITORS;
D O I
10.1016/j.stem.2011.12.013
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Cardiovascular disease is a leading cause of death worldwide. The limited capability of heart tissue to regenerate has prompted methodological developments for creating de novo cardiomyocytes, both in vitro and in vivo. Beyond uses in cell replacement therapy, patient-specific cardiomyocytes may find applications in drug testing, drug discovery, and disease modeling. Recently, approaches for generating cardiomyocytes have expanded to encompass three major sources of starting cells: human pluripotent stem cells (hPSCs), adult heart-derived cardiac progenitor cells (CPCs), and reprogrammed fibroblasts. We discuss state-of-the-art methods for generating de novo cardiomyocytes from hPSCs and reprogrammed fibroblasts, highlighting potential applications and future challenges.
引用
收藏
页码:16 / 28
页数:13
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