Suppr超能文献

马来酸伊索拉定对白细胞介素-8的调节作用参与消除伴放线放线杆菌诱导的缝隙连接细胞间通讯减少。

Regulation of IL-8 by Irsogladine maleate is involved in abolishment of Actinobacillus actinomycetemcomitans-induced reduction of gap-junctional intercellular communication.

作者信息

Fujita Tsuyoshi, Ashikaga Arata, Shiba Hideki, Uchida Yuushi, Hirono Chikara, Iwata Tomoyuki, Takeda Katsuhiro, Kishimoto Akiyoshi, Hirata Reika, Kawaguchi Hiroyuki, Shiba Yoshiki, Kurihara Hidemi

机构信息

Department of Periodontal Medicine, Division of Frontier Medical Science, Hiroshima University Graduate School of Biomedical Science, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.

出版信息

Cytokine. 2006 Jun;34(5-6):271-7. doi: 10.1016/j.cyto.2006.06.002. Epub 2006 Jul 25.

Abstract

Our previous report has shown that Irsogladine maleate (IM) counters and obviates the reduction in gap junction intercellular communication (GJIC) and the increase in IL-8 levels, respectively, induced by outer membrane protein 29 from Actinobacillus actinomycetemcomitans (A. actinomycetemcomitans) in cultured human gingival epithelial cells (HGEC). In addition, IM suppresses the increase in the secretion of IL-8 caused by whole live A. actinomycetemcomitans. These findings implicate the modulation of IL-8 levels by IM in abolishment of the reduction of GJIC in HGEC. Tight junctions are also responsible for cell-cell communication. Zonula occludens protein-1 (ZO-1) is a major tight junction protein. To investigate the regulatory mechanism of intercellular communication mediated by IM, in the present study, we focused on the involvement of IL-8 in A. actinomycetemcomitans-induced change in GJIC and ZO-1 expression in HGEC. IM countered the A. actinomycetemcomitans-induced reduction in levels of Connexin (CX) 43, suggesting that it could abolish the A. actinomycetemcomitans-induced reduction in GJIC in HGEC. CXCR-1 is a receptor of IL-8. The simultaneous addition of A. actinomycetemcomitans and anti-CXCR-1 antibody also abrogated the repression of GJIC and CX43 expression by A. actinomycetemcomitans in HGEC, although the anti-CXCR-1 antibody was less effective than IM. IM inhibited the IL-8-induced reduction in CX43 levels and GJIC in HGEC. IM countered the A. actinomycetemcomitans-induced reduction in the expression of ZO-1, although anti-CXCR-1 antibody did not influence the decrease in ZO-1 mRNA levels caused by A. actinomycetemcomitans. Furthermore, IL-8 had little effect on the mRNA levels of ZO-1. These findings suggest that IL-8 mediates the A. actinomycetemcomitans-induced reduction of GJIC and CX43 expression in HGEC. The regulation of IL-8 levels by IM in HGEC is partially involved in abrogation of the reduction of GJIC and CX43 expression by A. actinomycetemcomitans. Furthermore, the regulatory effect of IM on the expression of CX43 and ZO-1 is different.

摘要

我们之前的报告显示,马来酸伊索格拉定(IM)可对抗并消除伴放线放线杆菌(A. actinomycetemcomitans)外膜蛋白29在培养的人牙龈上皮细胞(HGEC)中诱导的间隙连接细胞间通讯(GJIC)减少和白细胞介素-8(IL-8)水平升高。此外,IM可抑制活的完整伴放线放线杆菌引起的IL-8分泌增加。这些发现表明,IM对IL-8水平的调节在消除HGEC中GJIC减少方面发挥作用。紧密连接也负责细胞间通讯。闭合蛋白-1(ZO-1)是一种主要的紧密连接蛋白。为了研究IM介导的细胞间通讯的调节机制,在本研究中,我们重点关注IL-8在伴放线放线杆菌诱导的HGEC中GJIC变化和ZO-1表达中的作用。IM对抗了伴放线放线杆菌诱导的连接蛋白(CX)43水平降低,表明它可以消除伴放线放线杆菌诱导的HGEC中GJIC减少。CXCR-1是IL-8的受体。同时添加伴放线放线杆菌和抗CXCR-1抗体也消除了伴放线放线杆菌对HGEC中GJIC和CX43表达的抑制作用,尽管抗CXCR-1抗体的效果不如IM。IM抑制了IL-8诱导的HGEC中CX43水平和GJIC降低。IM对抗了伴放线放线杆菌诱导的ZO-1表达减少,尽管抗CXCR-1抗体对伴放线放线杆菌引起的ZO-1 mRNA水平降低没有影响。此外,IL-8对ZO- mRNA水平影响很小。这些发现表明,IL-8介导了伴放线放线杆菌诱导的HGEC中GJIC和CX43表达减少。IM对HGEC中IL-8水平的调节部分参与了消除伴放线放线杆菌引起的GJIC和CX43表达减少。此外,IM对CX43和ZO-1表达的调节作用不同。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验