Bergin Philip James , Wen Sicheng , Pan-Hammarström Qiang , Quiding-Järbrink Marianne
{"title":"Secretion of matrix metalloproteinase-9 by macrophages, in vitro, in response to Helicobacter pylori","authors":"Bergin Philip James , Wen Sicheng , Pan-Hammarström Qiang , Quiding-Järbrink Marianne","doi":"10.1016/j.femsim.2005.03.008","DOIUrl":null,"url":null,"abstract":"<div><p><span>We have previously shown that matrix metalloproteinase-9 (MMP-9) activity is greatly enhanced within the active chronic inflammation of </span><span><span>Helicobacter pylori</span></span> infected individuals, of which a major fraction derives from macrophages in the tissue. Here, we have investigated the ability of macrophages to secrete MMPs in response to <em>H. pylori</em>. Human macrophages secrete MMP-9 in response to live and inactivated <em>H. pylori</em><span>, as well as to specific bacterial products. Protein kinase C<span><span>, phosphatiolylinositol 3-kinase and calcium uptake channels all play a role in MMP-9 secretion, whereas neither </span>tumour necrosis factor alpha, interleukin-8, nor interleukin-1β autocrine stimulation appear to contribute. We conclude that human macrophages have the ability to react directly against several </span></span><em>H. pylori</em><span> derived factors, utilising several signalling pathways.</span></p></div>","PeriodicalId":12220,"journal":{"name":"FEMS immunology and medical microbiology","volume":"45 2","pages":"Pages 159-169"},"PeriodicalIF":0.0000,"publicationDate":"2005-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.femsim.2005.03.008","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS immunology and medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928824405000921","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20
Abstract
We have previously shown that matrix metalloproteinase-9 (MMP-9) activity is greatly enhanced within the active chronic inflammation of Helicobacter pylori infected individuals, of which a major fraction derives from macrophages in the tissue. Here, we have investigated the ability of macrophages to secrete MMPs in response to H. pylori. Human macrophages secrete MMP-9 in response to live and inactivated H. pylori, as well as to specific bacterial products. Protein kinase C, phosphatiolylinositol 3-kinase and calcium uptake channels all play a role in MMP-9 secretion, whereas neither tumour necrosis factor alpha, interleukin-8, nor interleukin-1β autocrine stimulation appear to contribute. We conclude that human macrophages have the ability to react directly against several H. pylori derived factors, utilising several signalling pathways.