Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:17114467rdf:typepubmed:Citationlld:pubmed
pubmed-article:17114467lifeskim:mentionsumls-concept:C0079488lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0021760lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0024432lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0031715lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0033640lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0441471lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0030685lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C1523116lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0680255lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0205263lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0391871lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C1283071lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C1963578lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0205099lld:lifeskim
pubmed-article:17114467lifeskim:mentionsumls-concept:C0127400lld:lifeskim
pubmed-article:17114467pubmed:issue11lld:pubmed
pubmed-article:17114467pubmed:dateCreated2006-11-20lld:pubmed
pubmed-article:17114467pubmed:abstractTextHelicobacter pylori infection is associated with the local production of chemokines and cytokines, of which IL-6 is overexpressed at the margin of gastric ulcer in H. pylori-positive gastritis. Cells of the monocytic lineage are the major sources of IL-6, and mononuclear cell infiltration in the lamina propria is characteristic of H. pylori-induced chronic infection. Our study shows for the first time that a secreted peptidyl prolyl cis-, trans-isomerase, HP0175 elicits IL-6 gene expression and IL-6 release from macrophages. An isogenic strain inactivated in the HP0175 gene (knockout) was attenuated in its IL-6-inducing ability, which was restored after complementation with the HP0175 gene. The specificity of the HP0175-induced effect was confirmed by the fact that rHP0175 purified from HEK293 cells could also induce IL-6 release, ruling out the possibility that the observed effect was due to bacterial contaminants. HP0175 was capable of interacting directly with the extracellular domain of TLR4. HP0175-induced IL-6 gene expression was critically dependent on TLR4-dependent NF-kappaB and MAPK activation. TLR4/PI3K-dependent ERK1/2 and p38 MAPK signaling converged upon activation of mitogen- and stress-activated protein kinase 1 (MSK1). The central role of MSK1 was borne out by the fact that silencing of MSK1 expression abrogated HP0175-mediated NF-kappaB-dependent IL-6 gene transcription. MSK1 regulated the recruitment of p65 and phopho-Ser(10)-histone H3 to the IL-6 promoter. HP0175 therefore regulated IL-6 gene transcription through chromatin modification at the IL-6 promoter.lld:pubmed
pubmed-article:17114467pubmed:languageenglld:pubmed
pubmed-article:17114467pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:citationSubsetAIMlld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:17114467pubmed:statusMEDLINElld:pubmed
pubmed-article:17114467pubmed:monthDeclld:pubmed
pubmed-article:17114467pubmed:issn0022-1767lld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:BasuJoyotiJlld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:BanerjeeAnirb...lld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:KunduManikunt...lld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:Bhattacharyya...lld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:PathakShreshSlld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:PathakSushil...lld:pubmed
pubmed-article:17114467pubmed:authorpubmed-author:BasuSanchitaSlld:pubmed
pubmed-article:17114467pubmed:issnTypePrintlld:pubmed
pubmed-article:17114467pubmed:day1lld:pubmed
pubmed-article:17114467pubmed:volume177lld:pubmed
pubmed-article:17114467pubmed:ownerNLMlld:pubmed
pubmed-article:17114467pubmed:authorsCompleteYlld:pubmed
pubmed-article:17114467pubmed:pagination7950-8lld:pubmed
pubmed-article:17114467pubmed:dateRevised2009-11-19lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:meshHeadingpubmed-meshheading:17114467...lld:pubmed
pubmed-article:17114467pubmed:year2006lld:pubmed
pubmed-article:17114467pubmed:articleTitleTLR4-dependent NF-kappaB activation and mitogen- and stress-activated protein kinase 1-triggered phosphorylation events are central to Helicobacter pylori peptidyl prolyl cis-, trans-isomerase (HP0175)-mediated induction of IL-6 release from macrophages.lld:pubmed
pubmed-article:17114467pubmed:affiliationDepartment of Chemistry, Bose Institute, 93/1 Acharya Prafulla, Chandra Road, Kolkata 700009, India.lld:pubmed
pubmed-article:17114467pubmed:publicationTypeJournal Articlelld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17114467lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17114467lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17114467lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17114467lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:17114467lld:pubmed