Early dynamic fate changes in haemogenic endothelium characterized at the single-cell level

Nat Commun. 2013:4:2924. doi: 10.1038/ncomms3924.

Abstract

Haematopoietic stem cells (HSCs) are the founding cells of the adult haematopoietic system, born during ontogeny from a specialized subset of endothelium, the haemogenic endothelium (HE) via an endothelial-to-haematopoietic transition (EHT). Although recently imaged in real time, the underlying mechanism of EHT is still poorly understood. We have generated a Runx1 +23 enhancer-reporter transgenic mouse (23GFP) for the prospective isolation of HE throughout embryonic development. Here we perform functional analysis of over 1,800 and transcriptional analysis of 268 single 23GFP(+) HE cells to explore the onset of EHT at the single-cell level. We show that initiation of the haematopoietic programme occurs in cells still embedded in the endothelial layer, and is accompanied by a previously unrecognized early loss of endothelial potential before HSCs emerge. Our data therefore provide important insights on the timeline of early haematopoietic commitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Core Binding Factor Alpha 2 Subunit / genetics
  • Embryo, Mammalian / cytology*
  • Enhancer Elements, Genetic
  • Female
  • Gene Expression Regulation, Developmental*
  • Green Fluorescent Proteins / genetics
  • Hemangioblasts / cytology*
  • Hemangioblasts / physiology*
  • Male
  • Mice
  • Mice, Transgenic
  • Pregnancy
  • Single-Cell Analysis / methods*

Substances

  • Core Binding Factor Alpha 2 Subunit
  • Runx1 protein, mouse
  • Green Fluorescent Proteins

Associated data

  • GEO/GSE2075