Activation of endothelial nitric oxide synthase is critical for erythropoietin-induced mobilization of progenitor cells

The present study aimed to define the ability of erythropoietin (EPO) to mobilize hematopoietic stem cells (c-kit +/sca-1 +/lin-1 −; KSL-cells) and hematopoietic progenitor cells (CD34 + cells), including vascular endothelial growth factor receptor 2 expressing hematopoietic progenitor cells (CD34 +...

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Veröffentlicht in:Peptides (New York, N.Y. : 1980) N.Y. : 1980), 2008-08, Vol.29 (8), p.1451-1455
Hauptverfasser: Santhanam, Anantha Vijay R., d’Uscio, Livius V., Peterson, Timothy E., Katusic, Zvonimir S.
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Sprache:eng
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Zusammenfassung:The present study aimed to define the ability of erythropoietin (EPO) to mobilize hematopoietic stem cells (c-kit +/sca-1 +/lin-1 −; KSL-cells) and hematopoietic progenitor cells (CD34 + cells), including vascular endothelial growth factor receptor 2 expressing hematopoietic progenitor cells (CD34 +/Flk-1 + cells). We also sought to determine the role of endothelial nitric oxide synthase (eNOS) in EPO-induced mobilization. Wild type (WT) and eNOS −/− mice were injected bi-weekly with recombinant erythropoietin (EPO, 1000 U/kg, s.c.) for 14 days. EPO increased the number of KSL, CD34 +, CD34 +/Flk-1 + cells in circulating blood of wild type mice. These effects of EPO were abolished in eNOS −/− mice. Our results demonstrate that, EPO stimulates mobilization of hematopoietic stem and progenitor cells. This effect of EPO is critically dependent on activation of eNOS.
ISSN:0196-9781
1873-5169
DOI:10.1016/j.peptides.2008.03.016