Transcription Factor Levels after Forward Programming of Human Pluripotent Stem Cells with GATA1, FLI1, and TAL1 Determine Megakaryocyte versus Erythroid Cell Fate Decision

Stem Cell Reports. 2018 Dec 11;11(6):1462-1478. doi: 10.1016/j.stemcr.2018.11.001. Epub 2018 Nov 29.

Abstract

The production of blood cells and their precursors from human pluripotent stem cells (hPSCs) in vitro has the potential to make a significant impact upon healthcare provision. We demonstrate that the forward programming of hPSCs through overexpression of GATA1, FLI1, and TAL1 leads to the production of a population of progenitors that can differentiate into megakaryocyte or erythroblasts. Using "rainbow" lentiviral vectors to quantify individual transgene expression in single cells, we demonstrate that the cell fate decision toward an erythroblast or megakaryocyte is dictated by the level of FLI1 expression and is independent of culture conditions. Early FLI1 expression is critical to confer proliferative potential to programmed cells while its subsequent silencing or maintenance dictates an erythroid or megakaryocytic fate, respectively. These committed progenitors subsequently expand and mature into megakaryocytes or erythroblasts in response to thrombopoietin or erythropoietin. Our results reveal molecular mechanisms underlying hPSC forward programming and novel opportunities for application to transfusion medicine.

Keywords: erythroblast; forward programming; lineage fate decision; megakaryocyte; pluripotent stem cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Differentiation / drug effects
  • Cell Lineage* / drug effects
  • Cells, Cultured
  • Cytokines / pharmacology
  • Erythroid Cells / cytology*
  • Erythroid Cells / drug effects
  • Erythroid Cells / metabolism
  • Erythropoietin / pharmacology
  • GATA1 Transcription Factor / metabolism*
  • Gene Silencing
  • Humans
  • Megakaryocytes / cytology*
  • Megakaryocytes / drug effects
  • Megakaryocytes / metabolism
  • Pluripotent Stem Cells / cytology*
  • Pluripotent Stem Cells / drug effects
  • Pluripotent Stem Cells / metabolism
  • Proto-Oncogene Protein c-fli-1 / metabolism*
  • T-Cell Acute Lymphocytic Leukemia Protein 1 / metabolism*
  • Thrombopoietin / pharmacology
  • Transgenes

Substances

  • Cytokines
  • FLI1 protein, human
  • GATA1 Transcription Factor
  • GATA1 protein, human
  • Proto-Oncogene Protein c-fli-1
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Erythropoietin
  • TAL1 protein, human
  • Thrombopoietin