Transplantation Research Center and the Division of Nephrology, Department of Medicine, Children's Hospital Boston, MA 02115, USA.
J Immunol. 2010 Jan 15;184(2):545-9. doi: 10.4049/jimmunol.0900397. Epub 2009 Dec 11.
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.
在这项研究中,我们发现 CD4+ T 淋巴细胞的 CD45RO+记忆群体在 mRNA 和蛋白质水平上均表达血管内皮生长因子 (VEGF) 受体 KDR 和 Flt-1。此外,通过 Western blot 分析,我们发现 VEGF 增加了 CD4+CD45RO+ T 细胞中 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 和 CD4+CD45RO+ T 细胞中的药理学 KDR 抑制剂 SU5416 抑制。我们还发现 VEGF 以剂量依赖的方式(p < 0.001)增强有丝分裂原诱导的 IFN-γ产生,并显著(p < 0.05)增加该 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 VEGF 和 KDR 在 CD45RO+记忆 T 细胞反应中的新功能,这在免疫中可能具有重要的病理生理学意义。