OX40 induces CCL20 expression in the context of antigen stimulation: An expanding role of co-stimulatory molecules in chemotaxis

被引:8
作者
Zhong, Wenwei [3 ,4 ]
Zhang, Zili [3 ]
Hinrichs, David [2 ]
Wu, Xiumei [3 ]
Hall, Mark [3 ]
Xia, Zhenwei [4 ]
Rosenbaum, James T. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Casey Eye Inst, Portland, OR 97239 USA
[2] Portland VA Med Ctr, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR 97239 USA
[4] RuiJin Hosp, Dept Pediat, Shanghai 200025, Peoples R China
基金
美国国家卫生研究院;
关键词
CCL20; CD4+T cells; Co-stimulatory molecule; OX40; T cell co-stimulation; T-CELL FUNCTION; INFLAMMATORY PROTEIN-3-ALPHA; CYTOKINE DIFFERENTIATION; CHEMOKINE RECEPTOR; TH17; CELLS; ACTIVATION; INTERLEUKIN-8; MIGRATION; LIGAND; MEMORY;
D O I
10.1016/j.cyto.2010.03.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
OX40 is an inducible co-stimulatory molecule expressed by activated T cells. It plays an important role in the activation and proliferation of T lymphocytes. Recently, some co-stimulatory molecules have been shown to direct leukocyte trafficking. Chemotaxis is essential for achieving an effective immune response. CCL20 is an important chemoattractant produced by activated T cells. In this study, using DO11.10 mice whose transgenic T cell receptor specifically recognizes ovalbumin, we demonstrate that ovalbumin induces OX40 expression in CD4+ lymphocytes. Further stimulation of OX40 by OX40 activating antibody up-regulates CCL20 production. Both NF-kappa B dependent and independent signaling pathways are implicated in the induction of CCL20 by OX40. Finally, we primed the DO11.10 splenocytes with or without OX40 activating antibody in the presence of ovalbumin. Intranasal administration of the cell lysates derived from the cells with OX40 stimulation results in more severe leukocyte infiltration in the lung of DO11.10 mice, which is substantially attenuated by CCL20 blocking antibody. Taken together, this study has shown that activation of OX40 induces CCL20 expression in the presence of antigen stimulation. Thus, our results broaden the role of OX40 in chemotaxis, and reveal a novel effect of costimulatory molecules in orchestrating both T cell up-regulation and migration. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
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