Single-Cell Transcriptomic Analysis of Cardiac Differentiation from Human PSCs Reveals HOPX-Dependent Cardiomyocyte Maturation

Male Pluripotent Stem Cells 0301 basic medicine cardiomyocytes Mice, Transgenic heart 1307 Cell Biology Mice 03 medical and health sciences 1311 Genetics Mice, Inbred NOD Animals Humans Myocytes, Cardiac human pluripotent stem cells development Cells, Cultured Homeodomain Proteins Mice, Knockout Mice, Inbred C3H single-cell RNA-seq in silico lineage tracing Tumor Suppressor Proteins scdiff CRISPRi Cell Differentiation HOPX Mice, Inbred C57BL 1313 Molecular Medicine Female Single-Cell Analysis hypertrophy Transcriptome
DOI: 10.1016/j.stem.2018.09.009 Publication Date: 2018-10-04T10:51:50Z
ABSTRACT
Cardiac differentiation of human pluripotent stem cells (hPSCs) requires orchestration of dynamic gene regulatory networks during stepwise fate transitions but often generates immature cell types that do not fully recapitulate properties of their adult counterparts, suggesting incomplete activation of key transcriptional networks. We performed extensive single-cell transcriptomic analyses to map fate choices and gene expression programs during cardiac differentiation of hPSCs and identified strategies to improve in vitro cardiomyocyte differentiation. Utilizing genetic gain- and loss-of-function approaches, we found that hypertrophic signaling is not effectively activated during monolayer-based cardiac differentiation, thereby preventing expression of HOPX and its activation of downstream genes that govern late stages of cardiomyocyte maturation. This study therefore provides a key transcriptional roadmap of in vitro cardiac differentiation at single-cell resolution, revealing fundamental mechanisms underlying heart development and differentiation of hPSC-derived cardiomyocytes.
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