Thromb Haemost 2006; 95(04): 678-688
DOI: 10.1160/TH05-07-0511
Endothelium and Vascular Development
Schattauer GmbH

High urokinase expression contributes to the angiogenic properties of endothelial cells derived from circulating progenitors

Agnès Basire
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
2   Laboratoire d’Hématologie, Centre Hospitalier Universitaire La Conception, Marseille, France
,
Florence Sabatier
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
2   Laboratoire d’Hématologie, Centre Hospitalier Universitaire La Conception, Marseille, France
,
Sophie Ravet
2   Laboratoire d’Hématologie, Centre Hospitalier Universitaire La Conception, Marseille, France
,
Edouard Lamy
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
,
Agnès Mialhe
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
,
Gwladys Zabouo
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
,
Pascale Paul
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
2   Laboratoire d’Hématologie, Centre Hospitalier Universitaire La Conception, Marseille, France
,
Victor Gurewich
3   Vascular Research Laboratory, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA
,
José Sampol
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
,
Françoise Dignat-George
1   INSERM U608, Laboratoire d’Hématologie et d’Immunologie, UFR de Pharmacie, Université de la Méditerranée, Marseille, France
2   Laboratoire d’Hématologie, Centre Hospitalier Universitaire La Conception, Marseille, France
› Author Affiliations
Financial support: Network No 4CS01H Biotherapy INSERM.
Further Information

Publication History

Received 21 July 2005

Accepted after revision 08 February 2006

Publication Date:
30 November 2017 (online)

Summary

Endothelial progenitor cells (EPC) displaya unique ability to repair vascular injury and promote neovascularization although the underlying molecular mechanisms remain poorly understood. Urokinase-type plasminogen activator (uPA) and its receptor (uPAR) play a critical role in cell migration and angiogenesis by facilitating proteolysis of extracellular matrix.The aim of the present study was to characterize the uPA/uPAR-dependent proteolytic potential of EPC outgrown from human umbilical cord blood and to analyze its contribution to their angiogenic properties in vitro. Cells derived from EPC (EPDC), presenting typical features of late outgrowth endothelial cells, were compared to mature endothelial cells, represented by human umbilical vein endothelial cells (HUVEC). Using quantitative flow cytometry, enzyme-linked immunosorbent assays and zymography, we demonstrated that EPDC displayed higher levels of uPA and uPAR. In conditioned culture media, uPA-dependant proteolytic activity was also found to be significantly increased in EPDC.This activity was paralleled bya higher secretion of pro-metalloproteinase-2 (pro-MMP-2). Inhibition of EPDC-associated uPA by monoclonal antibodies that block either uPA activity or receptor binding, significantly reduced proliferation, migration and capillary like tube formation. Moreover, tumor necrosis factoralpha and vascular endothelial growth factor,known to be locally secreted in ischemic areas, further increased the proteolytic potential of EPDC by up-regulating uPA and uPAR expression respectively.The EPDC response to these factors was found to be more pronounced than that of HUVEC. In conclusion, these findings indicated that EPDC are characterized by high intrinsic uPA/uPAR-dependent proteolytic potential that could contribute to their invasive and angiogenic behaviour.

 
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