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 |
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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. |
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ISSN: | 0196-9781 1873-5169 |
DOI: | 10.1016/j.peptides.2008.03.016 |