Cutting Edge: Vascular Endothelial Growth Factor-Mediated Signaling in Human CD45RO+ CD4+ T Cells Promotes Akt and ERK Activation and Costimulates IFN-γ Production

被引:71
作者
Basu, Aninda
Hoerning, Andre
Datta, Dipak
Edelbauer, Monika
Stack, Maria P.
Calzadilla, Katiana
Pal, Soumitro
Briscoe, David M. [1 ]
机构
[1] Childrens Hosp, Div Nephrol, Dept Med, Boston, MA 02115 USA
基金
奥地利科学基金会; 美国国家卫生研究院;
关键词
FACTOR VEGF; DENDRITIC CELLS; CROSS-TALK; ANGIOGENESIS; NEUROPILIN-1; MIGRATION; RECEPTOR; POLARIZATION; INFLAMMATION; LYMPHOCYTES;
D O I
10.4049/jimmunol.0900397
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. The Journal of Immunology, 2010, 184: 545-549.
引用
收藏
页码:545 / 549
页数:5
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