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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Differential induction of cytokine genes and activation of mitogen-activated protein kinase family by soluble CD40 ligand and TNF in a human follicular dendritic cell line.
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Differential induction of cytokine genes and activation of mitogen-activated protein kinase family by soluble CD40 ligand and TNF in a human follicular dendritic cell line.

机译:人卵泡树突状细胞系中可溶性CD40配体和TNF的细胞因子基因的差异诱导和有丝分裂原激活的蛋白激酶家族的激活。

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Follicular dendritic cells (FDC)3 play crucial roles in germinal center (GC) formation and differentiation of GC B cells. Many aspects of FDC function are influenced by contact with B or T cells, and by cytokines produced in the GC, which involve stimulation of CD40 and TNF-alpha receptors on FDC. In this study, using an established FDC line, HK cells, we compared the effects of CD40 and TNF receptor triggering on cytokine induction and activation of mitogen-activated protein kinase family. We show that HK cells spontaneously produced IL-6, M-CSF, and G-CSF mRNA. Both the soluble form of CD40 ligand (sCD40L) and TNF increased the level of M-CSF and G-CSF mRNA. While TNF strongly induced IL-6 mRNA, its expression was not affected by sCD40L treatment, differing from the strong IL-6 induction in other cell types upon CD40 stimulation. In addition, sCD40L treatment resulted in activation of extracellular signal-related kinase 1 and 2 (ERK1/2) and p38 without significant increase in c-Jun N-terminal kinase (JNK) activity. Lack of JNK activation differs in that most B cells respond to CD40 stimulation by inducing JNK activity strongly, suggesting distinct characteristics of CD40 signaling in FDC. Compared with the effects of sCD40L, TNF was capable of inducing JNK activity in addition to the activation of ERK1/2 and p38. Furthermore, the proximal signaling elements activated by TNF differed from those activated by sCD40L, in that TNF did not require PMA-sensitive protein kinase C isoforms in the activation of ERK and p38, whereas sCD40L did. However, signals activated by these stimuli converged on cytokine gene expression in a synergistic manner, which may have implication in augmenting FDC function during GC reaction.
机译:滤泡树突状细胞(FDC)3在生发中心(GC)的形成和GC B细胞的分化中起关键作用。 FDC功能的许多方面受与B或T细胞的接触以及GC中产生的细胞因子的影响,这涉及刺激FDC上的CD40和TNF-α受体。在这项研究中,我们使用已建立的FDC系HK细胞,比较了CD40和TNF受体触发对细胞因子诱导和丝裂原活化蛋白激酶家族激活的影响。我们显示,HK细胞自发产生IL-6,M-CSF和G-CSF mRNA。 CD40配体(sCD40L)和TNF的可溶性形式均增加M-CSF和G-CSF mRNA的水平。尽管TNF强烈诱导IL-6 mRNA,但其表达不受sCD40L处理的影响,这不同于CD40刺激后其他细胞类型的强IL-6诱导作用。此外,sCD40L处理导致细胞外信号相关激酶1和2(ERK1 / 2)和p38的活化,而c-Jun N端激酶(JNK)活性却没有明显增加。缺乏JNK激活的不同之处在于,大多数B细胞通过强烈诱导JNK活性来对CD40刺激做出反应,这表明FDC中CD40信号传导的独特特征。与sCD40L的作用相比,除了激活ERK1 / 2和p38外,TNF还能够诱导JNK活性。此外,TNF激活的近端信号元件与sCD40L激活的元件不同,因为TNF在ERK和p38的激活中不需要PMA敏感的蛋白激酶C亚型,而sCD40L则需要。然而,由这些刺激激活的信号以协同方式收敛于细胞因子基因表达,这可能暗示着在GC反应过程中增强FDC功能。

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