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Rac1通过激活磷脂酰肌醇3激酶/蛋白激酶B通路来调节肽聚糖诱导的RAW 264.7巨噬细胞核因子-κB的激活以及环氧化酶-2的表达。

Rac1 regulates peptidoglycan-induced nuclear factor-kappaB activation and cyclooxygenase-2 expression in RAW 264.7 macrophages by activating the phosphatidylinositol 3-kinase/Akt pathway.

作者信息

Chen Bing-Chang, Kang Ju-Chiun, Lu Yen-Ta, Hsu Ming-Jen, Liao Chiao-Chun, Chiu Wen-Ta, Yeh Fu-Lung, Lin Chien-Huang

机构信息

School of Respiratory Therapy, College of Medicine, Taipei Medical University, Taipei, Taiwan.

出版信息

Mol Immunol. 2009 Mar;46(6):1179-88. doi: 10.1016/j.molimm.2008.11.006. Epub 2008 Dec 31.

Abstract

Previously, we found that peptidoglycan (PGN), a cell wall component of the gram-positive bacterium Staphylococcus aureus, may activate the Ras/Raf-1/extracellular signal-regulated kinase (ERK) pathway, which in turn initiates IkappaB kinases alpha/beta (IKKalpha/beta) and nuclear factor-kappaB (NF-kappaB) activation, and ultimately induces cyclooxygenase-2 (COX-2) expression in RAW 264.7 macrophages. In this study, we further investigated the roles of Rac1, phosphatidylinositol 3-kinase (PI3K), and Akt in PGN-induced NF-kappaB activation and COX-2 expression in RAW 264.7 macrophages. PGN-induced COX-2 expression was attenuated by a Rac1 dominant negative mutant (RacN17), PI3K inhibitors (wortmannin and LY 294002), and an Akt inhibitor (1L-6-hydroxymethyl-chiro-inositol2-[(R)-2-O-methyl-3-O-octadecylcarbonate]). PGN-induced PGE(2) release was also inhibited by RacN17. Treatment of RAW 264.7 macrophages with PGN caused the activation of Rac and Akt. PGN-induced Akt activation was inhibited by RacN17, LY 294002, and the Akt inhibitor. Stimulation of RAW 264.7 macrophages with PGN resulted in an increase in IKKalpha/beta phosphorylation and p65 Ser536 phosphorylation; these effects were inhibited by RacN17, LY 294002, an Akt inhibitor, and an Akt dominant negative mutant (AktDN). The PGN-induced increases in kappaB-luciferase activity were also inhibited by RacN17, wortmannin, LY 294002, an Akt inhibitor, and AktDN. Treatment of macrophages with PGN induced the recruitment of p85alpha and Rac1 to Toll-like receptor 2 (TLR2) in a time-dependent manner. These results indicate that PGN may activate the Rac1/PI3K/Akt pathway through the recruitment of p85alpha and Rac1 to TLR2 to mediate IKKalpha/beta activation and p65 phosphorylation, which in turn induces NF-kappaB transactivation, and ultimately causes COX-2 expression in RAW 264.7 macrophages.

摘要

此前,我们发现肽聚糖(PGN)是革兰氏阳性菌金黄色葡萄球菌的细胞壁成分,它可能激活Ras/Raf-1/细胞外信号调节激酶(ERK)通路,进而引发IκB激酶α/β(IKKα/β)和核因子κB(NF-κB)的激活,并最终诱导RAW 264.7巨噬细胞中环氧合酶-2(COX-2)的表达。在本研究中,我们进一步探究了Rac1、磷脂酰肌醇3激酶(PI3K)和Akt在PGN诱导的RAW 264.7巨噬细胞NF-κB激活及COX-2表达中的作用。PGN诱导的COX-2表达受到Rac1显性负性突变体(RacN17)、PI3K抑制剂(渥曼青霉素和LY 294002)以及Akt抑制剂(1L-6-羟甲基-手性-肌醇2-[(R)-2-O-甲基-3-O-十八烷基碳酸酯])的减弱。RacN17也抑制了PGN诱导的前列腺素E2(PGE2)释放。用PGN处理RAW 264.7巨噬细胞会导致Rac和Akt的激活。PGN诱导的Akt激活受到RacN17、LY 294002和Akt抑制剂的抑制。用PGN刺激RAW 264.7巨噬细胞会导致IKKα/β磷酸化和p65丝氨酸536磷酸化增加;这些效应受到RacN17、LY 294002、Akt抑制剂和Akt显性负性突变体(AktDN)的抑制。PGN诱导的κB-荧光素酶活性增加也受到RacN17、渥曼青霉素、LY 294002、Akt抑制剂和AktDN的抑制。用PGN处理巨噬细胞会以时间依赖性方式诱导p85α和Rac1募集到Toll样受体2(TLR2)。这些结果表明,PGN可能通过将p85α和Rac1募集到TLR2来激活Rac1/PI3K/Akt通路,从而介导IKKα/β激活和p65磷酸化,进而诱导NF-κB反式激活,并最终导致RAW 264.7巨噬细胞中COX-2的表达。

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