School of Biological Sciences, National Institute of Science Education and Research, HBNI, Bhubaneswar, Jatni, Khurda, 752050, Odisha, India.
Abgenex India Pvt Ltd, Bhubaneswar, India.
Sci Rep. 2018 May 8;8(1):7118. doi: 10.1038/s41598-018-25549-8.
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-γ, 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.
幼稚 T 细胞已知表达适度水平的 TLR4,而在 TCR 激活期间其水平会下降。然而,关于 TLR4 信号在 TCR 或有丝分裂原激活幼稚野生型 T 细胞中的作用的信息仍然很少。在这里,我们研究了在存在 VIPER 肽 (VP) 的情况下,幼稚小鼠 T 细胞在 TCR 和有丝分裂原刺激期间内源性 TLR4 的功能表达,VP 是一种已建立的 TLR4 信号抑制剂。正如预期的那样,我们发现 TLR4 的表达在 TCR 和有丝分裂原激活期间下降。有趣的是,我们观察到 VP 处理可恢复那些活化 T 细胞上的 TLR4 表达。此外,发现 VP 可调节幼稚 T 细胞的这种活化,如 CD25、CD69 表达、效应细胞因子(IL-2、IFN-γ、TNF)产生、T 细胞增殖和 T 细胞活化依赖性 Fas(CD95)、FasL(CD95L)表达的下调。总之,我们目前的观察结果强调了 TLR4 反应在 T 细胞中的可能需求,这可能对幼稚 T 细胞的致病性急性激活具有潜在意义。