CD144 (VE-cadherin) is transiently expressed by fetal liver hematopoietic stem cells

Injune Kim, Ömer H. Yilmaz, Sean J. Morrison

Research output: Contribution to journalArticlepeer-review

83 Scopus citations

Abstract

Hematopoietic stem cells (HSCs) and endothelial progenitors arise from a common embryonic precursor. However, these populations diverge prior to the onset of definitive hematopoiesis, as HSCs become CD45+ and are thought to lose the expression of endothelial markers. After the onset of definitive hematopoiesis, CD144 (vascular endothelial [VE]-cadherin) has been considered a specific marker of endothelial cells. In contrast, we found that virtually all HSC activity from embryonic day 13.5 (E13.5) fetal liver was CD144+. CD144 expression declined on E16.5 fetal liver HSCs and was absent from adult bone marrow HSCs. This identified a new marker that is differentially expressed between fetal and adult HSCs, and enhanced the purification of HSCs from the E13.5 fetal liver. These results emphasize the close developmental relationship between hematopoietic and endothelial cells, while indicating that CD144 is not a specific marker of endothelial cells during fetal development.

Original languageEnglish (US)
Pages (from-to)903-905
Number of pages3
JournalBlood
Volume106
Issue number3
DOIs
StatePublished - Aug 1 2005

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

Fingerprint

Dive into the research topics of 'CD144 (VE-cadherin) is transiently expressed by fetal liver hematopoietic stem cells'. Together they form a unique fingerprint.

Cite this