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Blood, 1 October 2005, Vol. 106, No. 7, pp. 2231-2232.
Circulating endothelial precursors: identification of functional subpopulationsUNIVERSITY OF FRANKFURT
The characterization of circulating endothelial progenitor cells is unclear. A recent study now provides evidence that the expression of the VEGF receptor 2 identifies a subpopulation of cells with endothelial regeneration activity within the CD14+ monocytic cells.
In this issue of Blood, Elsheikh and colleagues aimed to define the subpopulation within the monocytic cells, which exerts "EPC quality." The authors isolated CD14+ monocytic cells and purified the cells that expressed the vascular endothelial growth factor receptor 2 (VEGF-R2, or KDR). Expression of endothelial marker proteins and functional activity of the isolated cells was then determined. CD14+VEGF-R2+ cells express higher levels of endothelial marker proteins and formed tubes in vitro (see figure). Moreover, CD14+VEGF-R2+ but not CD14+ VEGF-R2- cells contributed to re-endothelialization after infusion of the cells in mice after denuding injury. These results are in accordance with previous studies demonstrating that CD34+VEGF-R2+ cells showed a better improvement of neovascularization after hind-limb ischemia compared with CD34+VEGF-R2- cells.2 These data implicate that VEGF-R2 expression is a major criterion to identify cells with a capacity to generate endothelial cells independent of whether they originate directly from hematopoietic stem cells or from monocytic cells.
One may speculate that the expression of VEGF-R2 is simply required to mediate signalling induced by its ligand, VEGF. However, CD14+VEGF-R+ as well as CD34+VEGF-R2+ also exhibited additional functional features. VEGF-R2+ cells showed a higher proliferation, migration, and growth factor release,2 (see figure) indicating that selection of VEGF-R2+ cells may enrich cells with a specific functional profile and potential "stemness" features. Indeed, pluripotent stem cells were restricted to the CD34+VEGF-R2+-cell fraction.3 Moreover, a specific subfraction of circulating CD14+ monocytic cells was recently shown to express the stem-cell markers Nanog and octamer-binding transcription factor 4 (oct-4).4 These Nanog+ monocytic cells were enriched in the VEGF-R2+ fraction and showed low expression of CD34. Whether these CD14+/CD34low/Nanog+ cells are representing the active fraction of CD14+/VEGF-R2+ cells isolated by Elsheikh et al remains to be elucidated. References
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