Maturing heart muscle cells: Mechanisms and transcriptomic insights

被引:16
|
作者
Murphy, Sean A. [1 ,2 ,3 ,4 ,5 ]
Chen, Elaine Zhelan [2 ]
Tung, Leslie [2 ]
Boheler, Kenneth R. [2 ]
Kwon, Chulan [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Cardiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Cellular & Mol Med, Baltimore, MD 21205 USA
关键词
Cardiomyocyte maturation; Pluripotent stem cells; Single-cell transcriptomics; Tissue engineering; Maturation metrics; Heart development; PLURIPOTENT STEM-CELLS; GAP-JUNCTION CHANNELS; CARDIAC DIFFERENTIATION; GENE-EXPRESSION; CARDIOMYOCYTES; MATURATION; MOUSE; ADULT; FETAL; PROLIFERATION;
D O I
10.1016/j.semcdb.2021.04.019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiomyocyte (CM) maturation is the transformation of differentiated fetal CMs into adult CMs that involves changes in morphology, cell function and metabolism, and the transcriptome. This process is, however, incomplete and ultimately arrested in pluripotent stem cell-derived CMs (PSC-CMs) in culture, which hinders their broad biomedical application. For this reason, enormous efforts are currently being made with the goal of generating mature PSC-CMs. In this review, we summarize key aspects of maturation observed in native CMs and discuss recent findings on the factors and mechanisms that regulate the process. Particular emphasis is put on transcriptional regulation and single-cell RNA-sequencing analysis that has emerged as a key tool to study timeseries gene regulation and to determine the maturation state. We then discuss different biomimetic strategies to enhance PSC-CM maturation and discuss their effects at the single cell transcriptomic and functional levels.
引用
收藏
页码:49 / 60
页数:12
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