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
AUTHORS (26)
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.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (51)
CITATIONS (245)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....