Human Pluripotent Stem Cell Fate Regulation by SMARCB1

Ilana Carmel-Gross, Etgar Levy, Leah Armon, Orly Yaron, Hiba Waldman Ben-Asher, Achia Urbach

Research output: Contribution to journalArticlepeer-review

Abstract

Epigenetic regulation by the SWI/SNF complex is essential for normal self-renewal capacity and pluripotency of human pluripotent stem cells (hPSCs). It has been shown that different subunits of the complex have a distinct role in this regulation. Specifically, the SMARCB1 subunit has been shown to regulate the activity of enhancers in diverse types of cells, including hPSCs. Here, we report the establishment of conditional hPSC lines, enabling control of SMARCB1 expression from complete loss of function to significant overexpression. Using this system, we show that any deviation from normal SMARCB1 expression leads to cell differentiation. We further found that SMARCB1 expression is not required for differentiation of hPSCs into progenitor cells, but rather for later stages of differentiation. Finally, we identify SMARCB1 as a critical player in regulation of cell-cell and cell-ECM interactions in hPSCs and show that this regulation is mediated at least in part by the WNT pathway.

Original languageEnglish
Pages (from-to)1037-1046
Number of pages10
JournalStem Cell Reports
Volume15
Issue number5
DOIs
StatePublished - 10 Nov 2020

Keywords

  • SMARCB1
  • SWI/SNF complex
  • extra cellular matrix
  • pluripotent stem cell

All Science Journal Classification (ASJC) codes

  • Genetics
  • Biochemistry
  • Cell Biology
  • Developmental Biology

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