VIPER regulates naive T cell activation and effector responses: Implication in TLR4 associated acute stage T cell responses

被引:7
|
作者
Sahoo, Subhransu Sekhar [1 ]
Pratheek, Belluru M. [1 ]
Meena, Vikram S. [1 ]
Nayak, Tapas Kumar [1 ]
Kumar, P. Sanjai [1 ]
Bandyopadhyay, Saumya [1 ]
Maiti, Prasanta Kumar [2 ]
Chattopadhyay, Subhasis [1 ]
机构
[1] HBNI, Natl Inst Sci Educ & Res, Sch Biol Sci, Khurja 752050, Odisha, India
[2] Abgenex India Pvt Ltd, Bhubaneswar, Odisha, India
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
INFLAMMATORY RESPONSE; CUTTING EDGE; RECEPTOR; EXPRESSION; MYD88; EXPANSION; RECOGNITION; SYSTEM; MODEL;
D O I
10.1038/s41598-018-25549-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Naive T cells are known to express the modest level of TLR4 while it is known to go down during TCR activation. However, information towards the requirement of TLR4 signaling during TCR or mitogenic activation of naive wild-type T cells remains scanty. Here we have investigated the endogenous functional expression of TLR4 in naive mice T cells during TCR and mitogenic stimulation in presence of VIPER peptide (VP), an established inhibitor of TLR4 signaling. As expected we found that TLR4 expression goes down during TCR and mitogenic activation. Interestingly, we observed that VP treatment restores TLR4 expression on those activated T cells. Moreover, VP was found to regulate such activation of naive T cell as evident by reduction of CD25, CD69 expression, effector cytokines (IL-2, IFN-gamma, TNF) production, T cell proliferation and down-regulation of T cell activation-dependent Fas (CD95), FasL (CD95L) expression. Together, our current observation highlights a possible requirement of TLR4 responses in T cells, which might have possible implication towards the pathogenic acute phase activation of naive T cells.
引用
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页数:9
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