首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Differential Regulation of CD44 Expression by Lipopolysaccharide (LPS) and TNF-alpha in Human Monocytic Cells: Distinct Involvement of c-Jun N-Terminal Kinase in LPS-Induced CD44 Expression
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Differential Regulation of CD44 Expression by Lipopolysaccharide (LPS) and TNF-alpha in Human Monocytic Cells: Distinct Involvement of c-Jun N-Terminal Kinase in LPS-Induced CD44 Expression

机译:脂多糖(LPS)和TNF-α在人单核细胞中CD44表达的差异调节:c-Jun N末端激酶在LPS诱导的CD44表达中的不同参与

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Alteractions in the regulation of CD44 expression play a critical role in modulating cell adhesion, migration, and inflammation. LPS, a bacterial cell wall component, regulates CD44 expression and may modulate CD44-mediated biological effects in monocytic cells during inflammation and immune responses. In this study, we show that in normal human monocytes, LPS and LPS-induced cytokines IL-10 and TNF-alpha enhance CD44 expression. To delineate the mechanism underlying LPS-induced CD44 expression, we investigated the role of the mitogen-activated protein kinase (MAPKs) p38, p42/44 extracellular signal-regulated kinase, and c-Jun N-terminal kinase (JNK) by using their specific inhibitors. We demonstrate the involvement, at least in part, fo p38 MAPK in THF-alpha-induced CD44 expression in both monocytes and promonocytic THF-1 cells. However, neither p38 nor p42/44 MAPKs were involved in IL-10-induced CD44 expression in monocytes. To further dissect the TNF-alpha and LPS-induced signaling pathways regulating CD44 expression independent of IL-10-mediated effects, we used IL-10 refractory THP-1 cells as a model system. Herein, we show that CD44 expression induced by the LPS-mediated pathway predominantly involved JNK activation. This conclusion was based on results derived by transfection of THP-1 cells with a dominant-negative mutant of stress-activated protein/extracellular signal-reglated kinase kinase 1, and by exposure of cells to JNK inhibitors dexamethasone and SP600125. All these treatments prevented CD44 induction in LPS-stimulated, but not in TNF-alpha-stimulated, THP-1 cells. Furthermore, we show that CD44 induction may involve JNK-dependent early growth response gene activation in LPS-stimulated monocytic cells. Taken together, these results suggest a predominant role o JNK in LPS-induced CD44 expression in monocytic cells.
机译:CD44表达调控中的变化在调节细胞粘附,迁移和炎症中起关键作用。 LPS是细菌细胞壁的一种成分,可调节CD44的表达,并可能在炎症和免疫反应期间调节单核细胞中CD44介导的生物学作用。在这项研究中,我们表明,在正常人单核细胞中,LPS和LPS诱导的细胞因子IL-10和TNF-α增强CD44的表达。为了描述LPS诱导的CD44表达的潜在机制,我们研究了有丝分裂原激活的蛋白激酶(MAPK)p38,p42 / 44细胞外信号调节激酶和c-Jun N端激酶(JNK)的作用。特异性抑制剂。我们证明,至少部分,fo p38 MAPK参与单核细胞和原单核细胞THF-1细胞中THF-α诱导的CD44表达。但是,p38和p42 / 44 MAPKs均不参与IL-10诱导的单核细胞CD44表达。为了进一步剖析独立于IL-10介导作用的,调节CD44表达的TNF-α和LPS诱导的信号通路,我们使用IL-10难治性THP-1细胞作为模型系统。在本文中,我们显示由LPS介导的途径诱导的CD44表达主要涉及JNK激活。该结论基于以下结果:通过用应力激活蛋白/细胞外信号调节激酶激酶1的显性负突变体转染THP-1细胞,以及将细胞暴露于JNK抑制剂地塞米松和SP600125而得出的结果。所有这些处理均阻止了LPS刺激的THP-1细胞中CD44的诱导,但TNF-α刺激的THP-1细胞中却没有阻止。此外,我们表明CD44诱导可能涉及LPS刺激的单核细胞中JNK依赖的早期生长反应基因激活。两者合计,这些结果表明JNK在LPS诱导的单核细胞CD44表达中起主要作用。

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