Generation and Analysis of GATA2w/eGFP Human ESCs Reveal ITGB3/CD61 as a Reliable Marker for Defining Hemogenic Endothelial Cells during Hematopoiesis

Stem Cell Reports. 2016 Nov 8;7(5):854-868. doi: 10.1016/j.stemcr.2016.09.008. Epub 2016 Oct 13.

Abstract

The transition from hemogenic endothelial cells (HECs) to hematopoietic stem/progenitor cells (HS/PCs), or endothelial to hematopoietic transition (EHT), is a critical step during hematopoiesis. However, little is known about the molecular determinants of HECs due to the challenge in defining HECs. We report here the generation of GATA2w/eGFP reporter in human embryonic stem cells (hESCs) to mark cells expressing GATA2, a critical gene for EHT. We show that during differentiation, functional HECs are almost exclusively GATA2/eGFP+. We then constructed a regulatory network for HEC determination and also identified a panel of positive or negative surface markers for discriminating HECs from non-hemogenic ECs. Among them, ITGB3 (CD61) precisely labeled HECs both in hESC differentiation and embryonic day 10 mouse embryos. These results not only identify a reliable marker for defining HECs, but also establish a robust platform for dissecting hematopoiesis in vitro, which might lead to the generation of HSCs in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Cell Differentiation* / genetics
  • Cell Line
  • Embryo, Mammalian
  • Embryonic Stem Cells / metabolism*
  • Endothelial Cells / cytology*
  • Endothelial Cells / metabolism*
  • GATA2 Transcription Factor / genetics*
  • GATA2 Transcription Factor / metabolism
  • Gene Expression Profiling
  • Gene Knock-In Techniques
  • Gene Targeting
  • Genes, Reporter
  • Genetic Vectors / genetics
  • Hematopoiesis* / genetics
  • Humans
  • Integrin beta3 / metabolism*
  • Mice
  • Multigene Family
  • Phenotype

Substances

  • Biomarkers
  • GATA2 Transcription Factor
  • ITGB3 protein, human
  • Integrin beta3