Induction of a hemogenic program in mouse fibroblasts

Cell Stem Cell. 2013 Aug 1;13(2):205-18. doi: 10.1016/j.stem.2013.05.024. Epub 2013 Jun 13.

Abstract

Definitive hematopoiesis emerges during embryogenesis via an endothelial-to-hematopoietic transition. We attempted to induce this process in mouse fibroblasts by screening a panel of factors for hemogenic activity. We identified a combination of four transcription factors, Gata2, Gfi1b, cFos, and Etv6, that efficiently induces endothelial-like precursor cells, with the subsequent appearance of hematopoietic cells. The precursor cells express a human CD34 reporter, Sca1, and Prominin1 within a global endothelial transcription program. Emergent hematopoietic cells possess nascent hematopoietic stem cell gene-expression profiles and cell-surface phenotypes. After transgene silencing and reaggregation culture, the specified cells generate hematopoietic colonies in vitro. Thus, we show that a simple combination of transcription factors is sufficient to induce a complex, dynamic, and multistep developmental program in vitro. These findings provide insights into the specification of definitive hemogenesis and a platform for future development of patient-specific stem and progenitor cells, as well as more-differentiated blood products.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Aggregation
  • Cell Lineage / genetics
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Colony-Forming Units Assay
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Green Fluorescent Proteins / metabolism
  • Hematopoiesis* / genetics
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Phenotype
  • Transcription Factors / metabolism

Substances

  • Biomarkers
  • Transcription Factors
  • Green Fluorescent Proteins

Associated data

  • GEO/GSE47497