Activation of macrophages by food antigens: enhancing effect of gluten on nitric oxide and cytokine production
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
10733090
DOI
10.1002/jlb.67.3.312
Knihovny.cz E-zdroje
- MeSH
- aktivace makrofágů imunologie MeSH
- aktivace transkripce účinky léků MeSH
- antigeny imunologie MeSH
- cytokiny biosyntéza imunologie metabolismus MeSH
- dusitany metabolismus MeSH
- gliadin chemická syntéza imunologie MeSH
- gluteny imunologie farmakologie MeSH
- interferon gama imunologie MeSH
- interleukin-10 biosyntéza metabolismus MeSH
- kultivované buňky MeSH
- messenger RNA genetika metabolismus MeSH
- myši inbrední BALB C MeSH
- myši inbrední C3H MeSH
- myši MeSH
- oxid dusnatý metabolismus MeSH
- peptidové fragmenty chemická syntéza imunologie MeSH
- peritoneální makrofágy účinky léků enzymologie imunologie metabolismus MeSH
- potraviny * MeSH
- synthasa oxidu dusnatého, typ II MeSH
- synthasa oxidu dusnatého genetika MeSH
- TNF-alfa biosyntéza metabolismus MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny MeSH
- cytokiny MeSH
- dusitany MeSH
- gliadin MeSH
- gluteny MeSH
- interferon gama MeSH
- interleukin-10 MeSH
- messenger RNA MeSH
- Nos2 protein, mouse MeSH Prohlížeč
- oxid dusnatý MeSH
- peptidové fragmenty MeSH
- synthasa oxidu dusnatého, typ II MeSH
- synthasa oxidu dusnatého MeSH
- TNF-alfa MeSH
Macrophages play an important role in effector mechanisms of various chronic inflammatory diseases. We studied the effect of gluten, the agent inducing celiac disease, and other food antigens on the activation of macrophages. Nitric oxide (NO) and cytokine production were followed as markers of activation, using cultured murine peritoneal macrophages. None of the food antigens tested caused direct inducible nitric oxide synthase (iNOS) activation in macrophages. Unlike other food antigens gluten, gliadin, and their proteolytic fragments significantly enhanced NO production when applied together with interferon-gamma (IFN-gamma), the most efficient being fragments originating from 25- to 45-min peptic digestion. The activation pathway was mediated via direct stimulation of tumor necrosis factor alpha (TNF-alpha) secretion. The NO-enhancing effect was confirmed at the level of iNOS mRNA transcription. In case of sustained local inflammatory reaction connected with increase of IFN-gamma, gluten and its proteolytic fragments may thus elevate NO production. Increased NO level could consequently participate in the development of mucosal lesions in the gut of celiac patients.
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