Thromb Haemost 2005; 94(04): 770-772
DOI: 10.1160/TH05-01-0038
Rapid and Short Communication
Schattauer GmbH

Nitric oxide differentially regulates proliferation and mobilization of endothelial progenitor cells but not of hematopoietic stem cells

Burcin Özüyaman*
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Petra Ebner*
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Ulrike Niesler
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Jutta Ziemann
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Petra Kleinbongard
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Thomas Jax
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Axel Gödecke
2   Institut für Herz- und Kreislaufphysiologie, Heinrich-Heine-Universität Düsseldorf, Germany
,
Malte Kelm
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
,
Christoph Kalka
1   Universitätsklinik Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Düsseldorf.
› Author Affiliations
Financial support:Supported by the Deutsche Forschungsgemeinschaft (SFB612) and the Forschungskommission Heinrich-Heine-Universität Düsseldorf (9772175CK)
Further Information

Publication History

Received18 January 2005

Accepter after resubmission17 June 2005

Publication Date:
07 December 2017 (online)

Summary

To investigate the role of nitric oxide in controlling endothelial progenitor (EPC) and hematopoietic stem cell (HSC) mobilization, wild-type mice, L-NAME treated WT and eNOS-/- mice received either PBS or G-CSF for 5 days. Under unstimulated conditions bone marrow of either L-NAME treated WT and eNOS-/- mice, representing acute and chronic NO-deficiency, showed higher CD34+Flk-1+ EPC numbers compared to their WT littermates. Furthermore, CD34+Flk-1+ progenitors under NO-deficient conditions showed a higher cell turn over since the proliferation and apoptosis activity underin vivo as well as in vitro conditions were enhanced. In line with this finding bone marrow derived EPC differentiation towards endothelial cells was modulated in an NO-dependent manner. Administration of G-CSF resulted in an increase of EPC within the bone marrow of WT animals with a consecutive release of these cells into the peripheral circulation. Under NO-deficient conditions G-CSF failed to increase EPC numbers. In contrast, the HSC population c-kit+Lin was not influenced by nitric oxide. Thus, NO differentially supports the mobilization of the endothelial committed progenitor subpopulation in bone marrow but does not have an effect on HSCin vivo.

* Both authors contributed equally


 
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