Distinct signaling. pathways regulate TLR2 co-stimulatory function in human T cells

被引:17
作者
Chapman, Nicole M. [1 ]
Bilal, Mahmood Y. [1 ]
Cruz-Orcutt, Noemi [2 ]
Knudson, Cory [1 ]
Madinaveitia, Sofia [3 ]
Light, Jonathan [3 ]
Houtman, Jon C. D. [1 ,3 ]
机构
[1] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Dent, Iowa City, IA 52242 USA
[3] Univ Iowa, Carver Coll Med, Dept Microbiol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
T cell receptor signaling; TLR2; co-stimulation; Human T cells; NF kappa B; Akt and Erk1/Erk2; TOLL-LIKE RECEPTORS; BRUTONS TYROSINE KINASE; BLOOD MONONUCLEAR-CELLS; DENDRITIC CELLS; ANTITUMOR-ACTIVITY; B-CELLS; ACTIVATION; EFFECTOR; TOLL-LIKE-RECEPTOR-2; STIMULATION;
D O I
10.1016/j.cellsig.2012.11.026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toll-like receptor 2 (TLR2) serves as a co-stimulatory receptor for human T cells by enhancing T cell receptor (TCR)-induced cytokine production and proliferation. However, it is unknown where signals from the TCR and TLR2 converge to enhance T cell activation. To address this gap, we examined changes in TCR-induced signaling following concurrent TLR2 activation in human T cells. Both proximal TCR-mediated signaling and early NF kappa B activation were not enhanced by TCR andTLR2 co-activation, potentially due to the association of TLR2 with TLR10. Instead, TLR2 co-induction did augment Akt and Erk1/Erk2 activation in human T cells. These findings demonstrate that TLR2 activates distinct signaling pathways in human T cells and suggest that alterations in expression of TLR2 co-receptors may contribute to aberrant T cell responses. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:639 / 650
页数:12
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