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首页> 外文期刊>FEBS letters. >LPS-induced chemokine expression in both MyD88-dependent and -independent manners is regulated by Cot/Tpl2-ERK axis in macrophages
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LPS-induced chemokine expression in both MyD88-dependent and -independent manners is regulated by Cot/Tpl2-ERK axis in macrophages

机译:LPS诱导的趋化因子表达以MyD88依赖性和非依赖性方式受巨噬细胞中Cot / Tpl2-ERK轴的调节

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摘要

LPS signaling is mediated through MyD88-dependent and -independent pathways, activating NF-κB, 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.
机译:LPS信号传导通过MyD88依赖性和非依赖性途径介导,激活NF-κB,MAP激酶和IRF3。 Cot / Tpl2是LPS介导的ERKs激活中必不可少的上游激酶。在这里,我们通过研究myd88-/-和cot / tpl2--/-巨噬细胞,探索MyD88和Cot / Tpl2在LPS诱导的趋化因子表达中的作用。在检查的9个LPS响应趋化因子中,ccl5,cxcl10和cxcl13的mRNA诱导是通过MyD88独立途径介导的。值得注意的是,Cot / Tpl2-ERK信号转导轴对这三种趋化因子的表达产生负面影响。相反,LPS诱导的ccl2,ccl7,cxcl2,cxcl3,ccl8和cxcl9的基因表达是以MyD88依赖性的方式介导的。 Cot / Tpl2-ERK轴促进前四个的表达,并抑制后两个的表达。因此,LPS通过巨噬细胞中的各种信号通路诱导多种趋化因子的表达。

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