Unraveling the Inconsistencies of Cardiac Differentiation Efficiency Induced by the GSK3β Inhibitor CHIR99021 in Human Pluripotent Stem Cells

  • Stem Cell Reports. 2018 Jun 5;10(6):1851-1866. doi: 10.1016/j.stemcr.2018.03.023.
Filip Laco  1 Tsung Liang Woo  2 Qixing Zhong  3 Radoslaw Szmyd  4 Sherwin Ting  2 Fahima Jaleel Khan  2 Christina L L Chai  3 Shaul Reuveny  2 Allen Chen  2 Steve Oh  5
Affiliations
  • 1. Bioprocessing Technology Institute, 20 Biopolis Way, Centros #06-01, Singapore 138668, Singapore. Electronic address: [email protected].
  • 2. Bioprocessing Technology Institute, 20 Biopolis Way, Centros #06-01, Singapore 138668, Singapore.
  • 3. Department of Pharmacy, Faculty of Science, National University of Singapore, 18 Science Drive 4, Singapore 117543, Singapore.
  • 4. Institute of Molecular and Cell Biology, 61 Biopolis Drive, Proteos #03-01, Singapore 138673, Singapore.
  • 5. Bioprocessing Technology Institute, 20 Biopolis Way, Centros #06-01, Singapore 138668, Singapore. Electronic address: [email protected].
Abstract

Cardiac differentiation efficiency is hampered by inconsistencies and low reproducibility. We analyzed the differentiation process of multiple human pluripotent stem cell (hPSC) lines in response to dynamic GSK3β inhibition under varying Cell Culture conditions. hPSCs showed strong differences in cell-cycle profiles with varying culture confluency. hPSCs with a higher percentage of cells in the G1 phase of the cell cycle exhibited cell death and required lower doses of GSK3β inhibitors to induce cardiac differentiation. GSK3β inhibition initiated cell-cycle progression via cyclin D1 and modulated both Wnt signaling and the transcription factor (TCF) levels, resulting in accelerated or delayed mesoderm differentiation. The TCF levels were key regulators during hPSC differentiation with CHIR99021. Our results explain how differences in hPSC lines and culture conditions impact cell death and cardiac differentiation. By analyzing the cell cycle, we were able to select for highly cardiogenic hPSC lines and increase the experimental reproducibility by predicting differentiation outcomes.

Keywords
CHIR99021; TCF7L1; cardiomyocytes; cell cycle; differentiation; pluripotent stem cells; β-catenin.