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  • Articles: DFG German National Licenses  (3)
  • gastric mucosal cells  (2)
  • INDUCIBLE NITRIC OXIDE SYNTHASE  (1)
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  • Articles: DFG German National Licenses  (3)
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  • 1
    ISSN: 1573-2568
    Keywords: GASTRIC EPITHELIAL CELLS ; OXIDATIVE STRESS ; NF-κB ; INDUCIBLE NITRIC OXIDE SYNTHASE
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The aim of this study was to revealoxidant-sensitive components in gastric epithelialcells, which may regulate inflammatory processes ingastric mucosa. Gel mobility shift assay showed thattreatment of cultured guinea pig gastric epithelial cellswith hydrogen peroxide or diamide produced a κBoligonucleotide-protein complex within 5 min. Thebinding proteins consisted of a p50/p65 heterodimer, which was identified by immunosupershift, UVcrosslinking, and immunoprecipitation analyses.Immunocytochemical study demonstrated that surfaceepithelial cells and parietal cells expressed p50 andp65 mainly in the cytosol, and the oxidants rapidlyinitiated the nuclear translocation of the components.The oxidants caused the up-regulation of p105 (a p50precursor) synthesis and the expression of inducible nitric oxide synthase mRNA. These resultssuggest that the oxidant-sensitive p50/p65 heterodimerin gastric epithelial cells may play an important rolein transcriptional activation of genes involved in inflammatory responses of thestomach.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 45 (2000), S. 291-297 
    ISSN: 1573-2568
    Keywords: apoptosis ; pit cell lineage ; caspase ; gastric mucosal cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The purpose of this study was to elucidate the mechanism of spontaneous and rapid cell death of cultured gastric pit cells. Gastric pit cells have a rapid cell turnover rate in vivo. We here show that guinea pig gastric pit cells in culture undergo spontaneous and rapid apoptotic DNA fragmentation, which may represent the rapid cell turnover cycle of gastric pit cells in vivo. This spontaneous apoptotic DNA fragmentation required the presence of fetal calf serum in the culture media. Furthermore, the spontaneous apoptotic DNA fragmentation was prevented by protein synthesis and caspase inhibitors.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-2568
    Keywords: geranylgeranylacetone ; gastric mucosal cells ; indomethacin ; heat-shock proteins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract One of the major side effects of nonsteroidal antiinflammatory drugs, such as indomethacin, is gastropathy. The purpose of this study was to search for a therapeutic drug to prevent this side effect in vitro. We found that geranylgeranylacetone, a unique antiulcer drug with a heat-shock protein-inducing ability, protected cultured guinea pig gastric mucosal cells from cell damage caused by indomethacin. This cytoprotective effect of geranylgeranylacetone required concentrations of more than 10−6 M and incubation periods of longer than 2 hr. Pretreatment of cells with an inhibitor of protein synthesis completely abolished the cytoprotective effect of geranylgeranylacetone, suggesting that some proteins induced by the drug are responsible for the cytoprotection. Since pretreatment of cells with low concentrations of ethanol, which also induced the heat-shock proteins, made cells resistant to indomethacin, heat-shock proteins are candidates for the proteins that are involved in the cytoprotective effect of geranylgeranylacetone against indomethacin.
    Type of Medium: Electronic Resource
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