Mitochondrial Maturation in Human Pluripotent Stem Cell Derived Cardiomyocytes

被引:66
作者
Dai, Dao-Fu [1 ,2 ]
Danoviz, Maria Elena [1 ]
Wiczer, Brian [1 ]
Laflamme, Michael A. [2 ,3 ]
Tian, Rong [1 ,2 ]
机构
[1] Univ Washington, Dept Anesthesiol & Pain Med, Mitochondria & Metab Ctr, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[3] Univ Hlth Network, Toronto Gen Res Inst, McEwen Ctr Regenerat Med, Toronto, ON, Canada
关键词
CARDIAC-MUSCLE; SARCOPLASMIC-RETICULUM; FUNCTIONAL MATURATION; HEART-FAILURE; DIFFERENTIATION; SKELETAL; EXPRESSION; PROMOTES; MYOCYTES; MICE;
D O I
10.1155/2017/5153625
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human pluripotent stem cells derived cardiomyocytes (PSC-CMs) have been widely used for disease modeling, drug safety screening, and preclinical cell therapy to regenerate myocardium. Most studies have utilized PSC-CM grown in vitro for a relatively short period after differentiation. These PSC-CMs demonstrated structural, electrophysiological, and mechanical features of primitive cardiomyocytes. A few studies have extended in vitro PSC-CM culture time and reported improved maturation of structural and electromechanical properties. The degree of mitochondrial maturation, however, remains unclear. This study characterized the development of mitochondria during prolonged in vitro culture. PSC-CM demonstrated an improved mitochondrial maturation with prolonged culture, in terms of increased mitochondrial relative abundance, enhanced membrane potential, and increased activity of several mitochondrial respiratory complexes. These are in parallel with the maturation of other cellular components. However, the maturation of mitochondria in PSC-CMs grown for extended in vitro culture exhibits suboptimal maturation when compared with the maturation of mitochondria observed in the human fetal heart during similar time interval.
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页数:10
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