Downregulation of vascular endothelial growth factor receptors by tumor necrosis factor-alpha in cultured human vascular endothelial cells. (original) (raw)

Research Article Free access | 10.1172/JCI118816

M A Perrella, W O Endege, M Yoshizumi, M E Lee, and E Haber

Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Cardiovascular Biology Laboratory, Harvard School of Public Health, Harvard Medical School, Massachusetts 02115, USA.

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Published July 15, 1996 -More info

Published July 15, 1996 -Version history

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Abstract

Vascular endothelial growth factor (VEGF) potently stimulates angiogenesis, whereas TNF-alpha has both pro- and anti-angiogenic activity. By measuring thymidine uptake, we found that TNF-alpha blocked a 2.3-fold increase in DNA synthesis induced by VEGF in human endothelial cells. To explore the possibility that the two interact to regulate endothelial cell proliferation, we examined the effect of TNF-alpha on VEGF receptor expression. In venous and arterial endothelial cells, TNF-alpha potently reduced mRNA transcripts of the two VEGF receptors (KDR/flk-1 and flt-1) in a dose- and time-dependent fashion. TNF-alpha at 1 ng/ml induced maximal inhibition of mRNA expression, which fell by approximately 70% after 24 h. TNF-alpha treatment did not significantly affect the KDR/flk-1 half-life but did decrease its rate of transcription to 40% of control. The decrease in KDR/flk-1 mRNA depended partially on new protein synthesis and was abolished by phorbol ester pretreatment. TNF-alpha decreased the amount of 35S-labeled KDR/flk-1 immunoprecipitated by an antibody specific for KDR/flk-1 to 18% of control. We conclude that TNF-alpha downregulates expression of both VEGF receptors in human endothelial cells and that this effect is transcriptional (at least for KDR/flk-1). These data support the hypothesis that TNF-alpha exerts its antiangiogenic effect in part by modulating the VEGF-specific angiogenic pathway.

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