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金黄色葡萄球菌溶血素 A 诱导人呼吸道上皮细胞释放白细胞介素 8 和白细胞介素 6 是通过激活 p38 和 Erk-MAP 激酶以及其他细胞类型特异性信号机制介导的。

S. aureus haemolysin A-induced IL-8 and IL-6 release from human airway epithelial cells is mediated by activation of p38- and Erk-MAP kinases and additional, cell type-specific signalling mechanisms.

机构信息

Animal Physiology and Biochemistry, Zoological Institute, Ernst Moritz Arndt University, Johann Sebastian Bach-Strasse 11/12, D-17487 Greifswald, Germany.

出版信息

Cell Microbiol. 2013 Jul;15(7):1253-65. doi: 10.1111/cmi.12113. Epub 2013 Feb 17.

DOI:10.1111/cmi.12113
PMID:23347173
Abstract

Soluble virulence-associated factors of Staphylococcus aureus like haemolysin A (Hla) induce secretion of chemo/cytokines from airway epithelial cells. To elucidate the potential roles of specific signalling pathways in this response, we treated 16HBE14o-, S9 or A549 cells with recombinant Hla (rHla). In a dose-dependent manner, rHla induced secretion of IL-8 in all three cell types, but IL-6 release only in 16HBE14o- and S9 cells. rHla-mediated secretion of IL-8 and IL-6 was suppressed by pre-incubation of cells with inhibitors of Erk type or p38 MAP kinases, indicating that activation of these signalling pathways is essential for IL-8 release in all three cell types and for IL-6 release in 16HBE14o- and S9 cells. The rHla-mediated phosphorylation and activation of p38 MAP kinase seem to depend on elevations in [Ca(2+)]i, an early response in rHla-treated cells. Inhibitors of calmodulin or calcium/calmodulin-dependent kinase II attenuated rHla-mediated release of IL-8 in 16HBE14o- and A549 cells and of IL-6 in 16HBE14o- cells. This indicates that rHla may mediate simultaneous activation of calmodulin-dependent processes as additional prerequisites for chemo/cytokine secretion.However, the inhibitors of calmodulin-dependent signalling did not affect rHla-induced p38 MAP kinase phosphorylation, indicating that this pathway works in parallel with p38 MAP kinase.

摘要

金黄色葡萄球菌可溶性毒力相关因子,如溶血素 A(Hla),可诱导气道上皮细胞分泌趋化/细胞因子。为了阐明特定信号通路在该反应中的潜在作用,我们用重组 Hla(rHla)处理 16HBE14o-、S9 或 A549 细胞。rHla 以剂量依赖性方式诱导这三种细胞类型分泌 IL-8,但仅在 16HBE14o-和 S9 细胞中诱导 IL-6 释放。用 Erk 型或 p38 MAP 激酶抑制剂预先孵育细胞可抑制 rHla 介导的 IL-8 和 IL-6 分泌,表明这些信号通路的激活对于三种细胞类型中 IL-8 的释放以及 16HBE14o-和 S9 细胞中 IL-6 的释放是必需的。rHla 介导的 p38 MAP 激酶磷酸化和激活似乎依赖于 [Ca(2+)]i 的升高,这是 rHla 处理细胞的早期反应。钙调蛋白或钙/钙调蛋白依赖性激酶 II 抑制剂可减弱 rHla 介导的 16HBE14o-和 A549 细胞中 IL-8 的释放以及 16HBE14o-细胞中 IL-6 的释放。这表明 rHla 可能介导钙调蛋白依赖性过程的同时激活,作为趋化/细胞因子分泌的其他前提条件。然而,钙调蛋白依赖性信号的抑制剂并不影响 rHla 诱导的 p38 MAP 激酶磷酸化,表明该途径与 p38 MAP 激酶平行工作。

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