Thromb Haemost 2009; 102(03): 544-554
DOI: 10.1160/TH08-12-0830
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

The VEGF-induced transcriptional response comprises gene clusters at the crossroad of angiogenesis and inflammation

Bernhard Schweighofer
1   Department of Vascular Biology and Thrombosis Research, Center for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Julia Testori
1   Department of Vascular Biology and Thrombosis Research, Center for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Caterina Sturtzel
1   Department of Vascular Biology and Thrombosis Research, Center for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Susanne Sattler
1   Department of Vascular Biology and Thrombosis Research, Center for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria
,
Herbert Mayer
4   Present address: Austrian Science Foundation, Vienna, Austria
,
Oswald Wagner
2   Clinical Department for Medical and Chemical Laboratory Diagnostics, Medical University of Vienna, Vienna,Austria
3   Ludwig Boltzmann Institute for Clinical and Experimental Oncology, Vienna, Austria
,
Martin Bilban
2   Clinical Department for Medical and Chemical Laboratory Diagnostics, Medical University of Vienna, Vienna,Austria
3   Ludwig Boltzmann Institute for Clinical and Experimental Oncology, Vienna, Austria
,
Erhard Hofer
1   Department of Vascular Biology and Thrombosis Research, Center for Biomolecular Medicine and Pharmacology, Medical University of Vienna, Vienna, Austria
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Publikationsverlauf

Received: 19. Dezember 2008

Accepted after major revision: 01. Juni 2009

Publikationsdatum:
22. November 2017 (online)

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Summary

VEGF-A is the major trigger of vasculogenesis and physiologic angiogenesis. We have investigated to which extent the gene repertoire induced by VEGF-A in endothelial cells is distinct from that of other growth factors and inflammatory cytokines. Genes upregulated in human umbilical vein endothelial cells treated with VEGF, EGF or IL-1 were compared by microarray analysis and clusters characteristic for individual or combinations of inducers were defined. VEGF-A upregulated in comparison to EGF a five-fold larger gene repertoire, which surprisingly overlapped to 60% with the inflammatory repertoire of IL-1. As shown by real-time RT-PCR for selected genes, VEGFinduction was mostly mediated by VEGF receptor-2 and the capacity of VEGF-A to induce genes in common with IL-1 largely depended on activation of the calcineurin/NFAT pathway, since cyclosporin A inhibited this induction. Another angiogenic growth factor, bFGF, did not share a comparable induction of inflammatory genes, but partially induced a small group of genes in common with VEGF-A, which were not regulated by EGF. Thus, the data display that VEGF-A induces a distinct gene repertoire, which, contrasting with other growth factors such as EGF or bFGF, includes an inherent inflammatory component possibly contributing to the cross-regulation of angiogenesis and inflammation as further indicated by the VEGF-mediated induction of leukocyte adhesion. Furthermore, a small group of genes selectively induced by VEGF-A with potential importance for angiogenesis is defined.