首页> 外文期刊>The journal of immunology >Cutting Edge: Vascular Endothelial Growth Factor-Mediated Signaling in Human CD45RO+ CD4+ T Cells Promotes Akt and ERK Activation and Costimulates IFN-γ Production
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Cutting Edge: Vascular Endothelial Growth Factor-Mediated Signaling in Human CD45RO+ CD4+ T Cells Promotes Akt and ERK Activation and Costimulates IFN-γ Production

机译:前沿:人类CD45RO + CD4 + T细胞中血管内皮生长因子介导的信号促进Akt和ERK激活并共刺激IFN-γ的产生

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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-γ 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.
机译:在这项研究中,我们发现CD4 + T淋巴细胞的CD45RO +记忆种群在mRNA和蛋白质水平上均表达了血管内皮生长因子(VEGF)受体KDR和Flt-1。此外,通过蛋白质印迹分析,我们发现VEGF增加了CD4 + CD45RO + T细胞内ERK和Akt的磷酸化和激活。这些VEGF介导的信号转导反应在表达VEGF受体的Jurkat T细胞系中被KDR特异性小干扰RNA抑制,在CD4 + CD45RO + T细胞中被药理学KDR抑制剂SU5416抑制。我们还发现,VEGF以剂量依赖的方式(p <0.001)增强了丝裂原诱导的IFN-γ的产生,并且显着(p <0.05)增加了该T细胞亚群的定向趋化性。总的来说,我们的结果首次定义了CD45RO +记忆T细胞反应中VEGF和KDR的新功能,这可能对免疫具有重要的病理生理意义。

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