Department of Oral Biochemistry, Field of Developmental Medicine, Kagoshima University, Graduate School of Medical and Dental Sciences, Sakuragaoka, Kagoshima, Japan.
FEBS Lett. 2012 May 21;586(10):1540-6. doi: 10.1016/j.febslet.2012.04.018. Epub 2012 Apr 21.
LPS signaling is mediated through MyD88-dependent and -independent pathways, activating NF-?B, MAP kinases and IRF3. Cot/Tpl2 is an essential upstream kinase in LPS-mediated activation of ERKs. Here we explore the roles of MyD88 and Cot/Tpl2 in LPS-induced chemokine expression by studying myd88(-/-) and cot/tpl2(-/-) macrophages. Among the nine LPS-responsive chemokines examined, mRNA induction of ccl5, cxcl10, and cxcl13 is mediated through the MyD88-independent pathway. Notably, Cot/Tpl2-ERK signaling axis exerts negative effects on the expression of these three chemokines. In contrast, LPS-induced gene expression of ccl2, ccl7, cxcl2, cxcl3, ccl8, and cxcl9 is mediated in the MyD88-dependent manner. The Cot/Tpl2-ERK axis promotes the expression of the first four and inhibits the expression of the latter two. Thus, LPS induces expression of multiple chemokines through various signaling pathways in macrophages.
LPS 信号通过 MyD88 依赖和非依赖途径进行传递,激活 NF-?B、MAP 激酶和 IRF3。Cot/Tpl2 是 LPS 介导的 ERK 激活中的必需上游激酶。在这里,我们通过研究 myd88(-/-)和 cot/tpl2(-/-)巨噬细胞,探讨了 MyD88 和 Cot/Tpl2 在 LPS 诱导趋化因子表达中的作用。在研究的 9 种 LPS 反应性趋化因子中,ccl5、cxcl10 和 cxcl13 的 mRNA 诱导是通过 MyD88 非依赖途径进行的。值得注意的是,Cot/Tpl2-ERK 信号轴对这三种趋化因子的表达产生负向影响。相比之下,LPS 诱导的 ccl2、ccl7、cxcl2、cxcl3、ccl8 和 cxcl9 的基因表达是通过 MyD88 依赖方式进行的。Cot/Tpl2-ERK 轴促进前四种趋化因子的表达,抑制后两种趋化因子的表达。因此,LPS 通过多种信号通路在巨噬细胞中诱导多种趋化因子的表达。