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Single-cell transcriptomic analysis of cardiac differentiation from human PSCs reveals HOPX-dependent cardiomyocyte maturation


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.

Type Journal
ISBN 1875-9777
Authors Friedman, C. E.; Nguyen, Q.; Lukowski, S. W.; Helfer, A.; Chiu, H. S.; Miklas, J.; Levy, S.; Suo, S.; Han, J. J.; Osteil, P.; Peng, G.; Jing, N.; Baillie, G. J.; Senabouth, A.; Christ, A. N.; Bruxner, T. J.; Murry, C. E.; Wong, E. S.; Ding, J.; Wang, Y.; Hudson, J.; Ruohola-Baker, H.; Bar-Joseph, Z.; Tam, P. P. L.; Powell, J. E.; Palpant, N. J.
Responsible Garvan Author Dr Joseph Powell
Publisher Name Cell Stem Cell
Published Date 2018-10-04
Published Volume 23
Published Issue 4
Published Pages 586-598
Status Published in-print
DOI 10.1016/j.stem.2018.09.009
URL link to publisher's version