Transient stabilization of human cardiovascular progenitor cells from human pluripotent stem cells in vitro reflects stage-specific heart development in vivo

Cardiovasc Res. 2024 Sep 21;120(11):1295-1311. doi: 10.1093/cvr/cvae118.

Abstract

Aims: Understanding the molecular identity of human pluripotent stem cell (hPSC)-derived cardiac progenitors and mechanisms controlling their proliferation and differentiation is valuable for developmental biology and regenerative medicine.

Methods and results: Here, we show that chemical modulation of histone acetyl transferases (by IQ-1) and WNT (by CHIR99021) synergistically enables the transient and reversible block of directed cardiac differentiation progression on hPSCs. The resulting stabilized cardiovascular progenitors (SCPs) are characterized by ISL1pos/KI-67pos/NKX2-5neg expression. In the presence of the chemical inhibitors, SCPs maintain a proliferation quiescent state. Upon small molecules, removal SCPs resume proliferation and concomitant NKX2-5 up-regulation triggers cell-autonomous differentiation into cardiomyocytes. Directed differentiation of SCPs into the endothelial and smooth muscle lineages confirms their full developmental potential typical of bona fide cardiovascular progenitors. Single-cell RNA-sequencing-based transcriptional profiling of our in vitro generated human SCPs notably reflects the dynamic cellular composition of E8.25-E9.25 posterior second heart field of mouse hearts, hallmarked by nuclear receptor sub-family 2 group F member 2 expression. Investigating molecular mechanisms of SCP stabilization, we found that the cell-autonomously regulated retinoic acid and BMP signalling is governing SCP transition from quiescence towards proliferation and cell-autonomous differentiation, reminiscent of a niche-like behaviour.

Conclusion: The chemically defined and reversible nature of our stabilization approach provides an unprecedented opportunity to dissect mechanisms of cardiovascular progenitors' specification and reveal their cellular and molecular properties.

Keywords: Histone acetyl transferases; Second heart field; Small molecules; WNT pathway; hPSC-derived cardiovascular progenitors.

MeSH terms

  • Animals
  • Cell Differentiation*
  • Cell Line
  • Cell Lineage
  • Cell Proliferation*
  • Gene Expression Regulation, Developmental*
  • Heart
  • Homeobox Protein Nkx-2.5* / genetics
  • Homeobox Protein Nkx-2.5* / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / enzymology
  • Induced Pluripotent Stem Cells / metabolism
  • LIM-Homeodomain Proteins / genetics
  • LIM-Homeodomain Proteins / metabolism
  • Mice
  • Myocytes, Cardiac* / enzymology
  • Myocytes, Cardiac* / metabolism
  • Myocytes, Smooth Muscle / metabolism
  • Phenotype
  • Pyridines* / pharmacology
  • Pyrimidines* / pharmacology
  • Single-Cell Analysis
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Wnt Signaling Pathway

Substances

  • Chir 99021
  • Homeobox Protein Nkx-2.5
  • NKX2-5 protein, human
  • Pyrimidines
  • Pyridines
  • insulin gene enhancer binding protein Isl-1
  • Transcription Factors
  • LIM-Homeodomain Proteins