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Distinct regulation of CD40-mediated interleukin-6 and interleukin-12 productions via mitogen-activated protein kinase and nuclear factor κB-inducing kinase in mature dendritic cells

机译:在成熟树突状细胞中通过促分裂原活化蛋白激酶和核因子κB诱导激酶对CD40介导的白介素6和白介素12产生的不同调节

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摘要

The role of mitogen-activated protein kinase (MAPK) and nuclear factor κB (NF-κB) pathways, especially NF-κB-inducing kinase (NIK)-mediated alternative pathway, in CD40-mediated interleukin (IL)-6 and IL-12 productions by immature or mature dendritic cells (DCs) was investigated. Murine myeloid DCs were matured by treatment with lipopolysaccharide. CD40 ligation induced modest or vigorous cytokine productions in immature or mature DCs, respectively. After CD40 ligation, p38 MAPK was significantly activated in either immature or mature DCs. SB203580, a p38 MAPK inhibitor, markedly decreased CD40-mediated IL-6 and IL-12 productions in immature DCs. In mature DCs, SB203580 significantly decreased CD40-mediated IL-6 but not IL-12 production. On the other hand, CD40 ligation induced vigorous activation of the NF-κB alternative pathway including p100 phosphorylation and subsequent nuclear translocations of p52, a processed form of p100, and RelB in mature but not immature DCs. The CD40-mediated phosphorylation of p100 was completely abolished in NIK-mutated mature DCs. The NIK mutation markedly reduced CD40-mediated IL-12 but not IL-6 production by mature DCs. Taken together, we concluded that IL-6 and IL-12 productions in response to CD40 ligation were controlled by p38 MAPK and NIK mediated alternative pathway, respectively, in mature DCs.
机译:丝裂原活化蛋白激酶(MAPK)和核因子κB(NF-κB)途径,尤其是NF-κB诱导激酶(NIK)介导的替代途径在CD40介导的白介素(IL)-6和IL-研究了未成熟或成熟的树突状细胞(DC)的12种产物。通过用脂多糖处理使鼠骨髓DCs成熟。 CD40连接分别在未成熟或成熟的DC中诱导适度或剧烈的细胞因子产生。 CD40连接后,p38 MAPK在未成熟或成熟的DC中均被显着激活。 SB203580是p38 MAPK抑制剂,可显着降低未成熟DC中CD40介导的IL-6和IL-12产生。在成熟的DC中,SB203580显着降低CD40介导的IL-6产生,但不降低IL-12产生。另一方面,CD40连接诱导了NF-κB替代途径的剧烈活化,包括成熟但非成熟DC中p100的磷酸化以及随后的p52,p100的加工形式和RelB的核易位。在NIK突变的成熟DC中,CD40介导的p100磷酸化被完全消除。 NIK突变显着降低了成熟DC产生的CD40介导的IL-12,但没有降低IL-6的产生。两者合计,我们得出结论,在成熟DC中,响应CD40连接的IL-6和IL-12的产生分别受p38 MAPK和NIK介导的替代途径控制。

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