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Signaling events involved in cytokine and chemokine production induced by secretory phospholipase A2 in human lung macrophages

机译:在人肺巨噬细胞中由分泌性磷脂酶a2诱导的细胞因子和趋化因子产生中涉及的信号传导事件

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摘要

Secretory phospholipases A(2) (sPLA(2)) are enzymes released during inflammatory reactions. These molecules activate immune cells by mechanisms either related or unrelated to their enzymatic activity. We examined the signaling events activated by group IA (GIA) and group IB (GIB) sPLA(2) in human lung macrophages leading to cytokine/chemokine production. sPLA(2) induced the production of cytokines (TNF-alpha, IL-6 and IL-10) and chemokines (CCL2, CCL3, CCL4 and CXCL8), whereas no effect was observed on IL-12, CCL1, CCL5 and CCL22. sPLA(2) induced the phosphorylation of the MAPK p38 and ERK1/2, and inhibition of these kinases by SB203580 and PD98059, respectively, reduced TNF-alpha and CXCL8 release. Suppression of sPLA(2) enzymatic activity by a site-directed inhibitor influenced neither cytokine/chemokine production nor activation of MAPK, whereas alteration of sPLA(2) secondary structure suppressed both responses. GIA activated the phosphatidylinositol 3-kinase (PI3 K)/Akt system and a specific inhibitor of PI3 K (LY294002) reduced sPLA(2)-induced release of TNF-alpha and CXCL8. GIA promoted phosphorylation and degradation of IkappaB and inhibition of NF-kappaB by MG-132 and 6-amino-4-phenoxyphenylethylamino-quinazoline suppressed the production of TNF-alpha and CXCL8. These results indicate that sPLA(2) induce the production of cytokines and chemokines in human macrophages by a non-enzymatic mechanism involving the PI3 K/Akt system, the MAPK p38 and ERK1/2 and NF-kappaB.
机译:分泌型磷脂酶A(2)(sPLA(2))是在炎症反应过程中释放的酶。这些分子通过与其酶活性相关或无关的机制激活免疫细胞。我们在人肺巨噬细胞中检测了由IA(GIA)组和IB(GIB)sPLA(2)组激活的信号传导事件,导致细胞因子/趋化因子的产生。 sPLA(2)诱导了细胞因子(TNF-α,IL-6和IL-10)和趋化因子(CCL2,CCL3,CCL4和CXCL8)的产生,而对IL-12,CCL1,CCL5和CCL22没有影响。 sPLA(2)诱导MAPK p38和ERK1 / 2的磷酸化,并分别由SB203580和PD98059抑制这些激酶,从而降低TNF-α和CXCL8的释放。定点抑制剂抑制sPLA(2)的酶活性既不影响细胞因子/趋化因子的产生,也不影响MAPK的激活,而sPLA(2)二级结构的改变抑制了这两种反应。 GIA激活了磷脂酰肌醇3激酶(PI3 K)/ Akt系统,PI3 K的特异性抑制剂(LY294002)减少了sPLA(2)诱导的TNF-α和CXCL8释放。 GIA促进MG-132和6-氨基-4-苯氧基苯基乙基氨基-喹唑啉对IkappaB的磷酸化和降解以及对NF-kappaB的抑制,从而抑制了TNF-α和CXCL8的产生。这些结果表明,sPLA(2)通过涉及PI3 K / Akt系统,MAPK p38和ERK1 / 2以及NF-κB的非酶机制诱导人巨噬细胞中细胞因子和趋化因子的产生。

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