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dc.contributor.author Molnár, Kriszta
dc.contributor.author Vannay, Ádám
dc.contributor.author Sziksz, Erna
dc.contributor.author Bánki, Nóra Fanni
dc.contributor.author Győrffy, Hajnalka
dc.contributor.author Arató, András
dc.contributor.author Dezsőfi, Antal
dc.contributor.author Veres, Gábor
dc.date.accessioned 2017-01-09T12:29:17Z
dc.date.available 2017-01-09T12:29:17Z
dc.date.issued 2012
dc.identifier 84859932272
dc.identifier.citation pagination=157-161; journalVolume=460; journalIssueNumber=2; journalTitle=VIRCHOWS ARCHIV;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3923
dc.identifier.uri doi:10.1007/s00428-011-1188-5
dc.description.abstract A major function of the enzyme intestinal alkaline phosphatase (iAP) is the detoxification of lipopolysaccharide (LPS), the ligand of Toll-like receptor 4 (TLR4). Hence, iAP has a role in the defence of maintaining intestinal barrier integrity. As intestinal barrier integrity is impaired in coeliac disease (CD), we tested the expression and localization of iAP in duodenal mucosa specimens from children with newly diagnosed CD (n = 10), with CD on gluten-free diet (GFD) (n = 5) and compared to those from ten healthy children. The mRNA and protein expression was determined by RT-PCR and Western blot analysis, respectively. Tissue localization of iAP and TLR4 was determined by immunofluorescence staining. iAP protein expression level was significantly lower than normal in newly diagnosed CD, while it was normalised in children on GFD. iAP and TLR4 colocalized at the epithelial surface of duodenal mucosa in each group of subjects enrolled. The finding of decreased iAP protein levels in newly diagnosed CD is consistent with its role in decreased intestinal barrier integrity. The latter may be the result of decreased LPS-detoxifying ability.
dc.relation.ispartof urn:issn:0945-6317
dc.title Decreased mucosal expression of intestinal alkaline phosphatase in children with coeliac disease
dc.type Journal Article
dc.date.updated 2016-12-09T10:41:45Z
dc.language.rfc3066 en
dc.identifier.mtmt 1824688
dc.identifier.wos 000301546700005
dc.identifier.pubmed 22262031
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/AOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport
dc.contributor.department SE/AOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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