The Journal of Immunology · 2009 · 85 citations · 17 references
Life SciencesImmunologyMolecular BiologyCell SignalingGene ExpressionSignal TransductionAngiogenesisCytokine Receptor SignalingGrowth Factor SignalingHelper T Cell SubsetsInflammatory SignalingCd4 Positive T CellsErk SignalingProtein Expression LevelsReceptorsVascular Endothelial Growth FactorVascular Endothelial Growth Factor Receptor SignalingVascular Endothelial Growth Factor ReceptorsVascular Endothelial Growth Factor Signaling
In this study, we find that CD45RO+ memory populations of CD4+ T lymphocytes express the vascular endothelial growth factor (VEGF) receptors KDR and Flt-1 at both the mRNA and protein levels. Furthermore, by Western blot analysis, we find that VEGF increases the phosphorylation and activation of ERK and Akt within CD4+CD45RO+ T cells. These VEGF-mediated signaling responses were inhibited by a KDR-specific small interfering RNA in a VEGF receptor-expressing Jurkat T cell line and by SU5416, a pharmacological KDR inhibitor, in CD4+CD45RO+ T cells. We also find that VEGF augments mitogen-induced production of IFN-gamma in a dose-dependent manner (p < 0.001) and significantly (p < 0.05) increases directed chemotaxis of this T cell subset. Collectively, our results for the first time define a novel function for VEGF and KDR in CD45RO+ memory T cell responses that are likely of great pathophysiological importance in immunity.
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Autocrine stimulation of VEGFR-2 activates human leukemic cell growth and migration
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Medicine, Cancer Biology, Oncology +17
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