Distinct hemogenic potential of endothelial cells and CD41+ cells in mouse embryos

Dev Growth Differ. 2007 May;49(4):287-300. doi: 10.1111/j.1440-169X.2007.00925.x.

Abstract

Definitive hematopoietic progenitor cells have been thought to develop from the vascular endothelium located in the aorta-gonad-mesonephros region of the mouse embryo. However, several recent findings have suggested that most hematopoietic progenitors are derived from non-endothelial precursor cells expressing CD41. We characterized two distinct precursor populations of definitive hematopoietic cell lineages, vascular endothelial (VE)-cadherin(+) CD41(-) CD45(-) endothelial cells and CD41(+) CD45(-) non-endothelial progenitors, both of which are derived from lateral mesoderm. VE-cadherin(+) endothelial cells obtained from cultures of differentiating embryonic stem cells possessed hematopoietic potential encompassing erythroid, myeloid and B lymphoid lineages, whereas CD41(+) progenitors lacked the B lymphopoietic potential. VE-cadherin(+) endothelial cells in the lower trunk of the embryo proper showed a significant potential for initiating B lymphopoiesis in cultures, while endothelial cells in the yolk sac appeared to have a bias for myeloerythropoietic differentiation. CD41(+) progenitors isolated from yolk sac and embryo proper were capable of generating multiple hematopoietic lineages, although mast cell precursors were exclusively enriched in CD41(+) progenitors in the yolk sac. These results suggest that hemogenic endothelial cells and CD41(+) progenitors possess distinct hematopoietic potential depending on the tissues in which they reside.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD / analysis
  • Cadherins / analysis
  • Cell Differentiation
  • Cell Line
  • Embryo, Mammalian / cytology*
  • Embryo, Mammalian / metabolism
  • Embryonic Development
  • Embryonic Stem Cells / cytology
  • Endothelial Cells / cytology*
  • Female
  • Hematopoiesis*
  • Hematopoietic Stem Cells / cytology*
  • Lymphopoiesis
  • Mast Cells / cytology
  • Mesoderm / cytology
  • Mice
  • Mice, Inbred ICR
  • Platelet Membrane Glycoprotein IIb / analysis*
  • Pregnancy
  • Stromal Cells / cytology
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism
  • Yolk Sac / cytology

Substances

  • Antigens, CD
  • Cadherins
  • Platelet Membrane Glycoprotein IIb
  • cadherin 5
  • Vascular Endothelial Growth Factor Receptor-2