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Helicobacter pylori gamma-glutamyl transpeptidase-induced Ca2+ release via PLC-IP3 receptors in AGS cells

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dc.contributor.authorPark, Eun-Hee-
dc.contributor.authorKim, Jung-Min-
dc.contributor.authorKim, Kyung-Mi-
dc.contributor.authorKang, Dawon-
dc.contributor.authorCho, Young-Ah-
dc.contributor.authorChoi, Jun-Young-
dc.contributor.authorSong, Jea-Young-
dc.contributor.authorKang, Hyung-Lyun-
dc.contributor.authorLee, Woo-Kon-
dc.contributor.authorCho, Myung-Je-
dc.contributor.authorRhee, Kwang-Ho-
dc.contributor.authorSeo, Ji-Hyun-
dc.contributor.authorYoun, Hee-Shang-
dc.contributor.authorBaik, Seung-Chul-
dc.date.accessioned2022-12-26T22:49:46Z-
dc.date.available2022-12-26T22:49:46Z-
dc.date.issued2014-12-
dc.identifier.issn0008-4166-
dc.identifier.issn1480-3275-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/18643-
dc.description.abstractIn our previous study, gamma-glutamyl transpeptidase (GGT) isolated from Helicobacter pylori induced apoptosis of AGS cells. Here, we investigate Ca2+ effects on GGT-induced apoptosis. The GGT transiently and significantly increased intracellular Ca2+ concentration ([Ca2+](i)) in AGS cells in a dose-dependent manner (P < 0.05). The GGT-induced Ca2+ increase resulted from Ca2+ influx and release through the phospholipase C - inositol 1,4,5-trisphosphate (PLC-IP3) pathway. The GGT-induced apoptosis was significantly reduced by treatment with U73122 (a PLC inhibitor) and xestospongin (an IP3 receptor antagonist) (P < 0.05). These results indicate that GGT could induce apoptosis of AGS cells by high levels of [Ca2+](i).-
dc.format.extent4-
dc.language영어-
dc.language.isoENG-
dc.publisherCANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS-
dc.titleHelicobacter pylori gamma-glutamyl transpeptidase-induced Ca2+ release via PLC-IP3 receptors in AGS cells-
dc.typeArticle-
dc.publisher.location캐나다-
dc.identifier.doi10.1139/cjm-2014-0464-
dc.identifier.scopusid2-s2.0-84912026921-
dc.identifier.wosid000345536300010-
dc.identifier.bibliographicCitationCANADIAN JOURNAL OF MICROBIOLOGY, v.60, no.12, pp 865 - 868-
dc.citation.titleCANADIAN JOURNAL OF MICROBIOLOGY-
dc.citation.volume60-
dc.citation.number12-
dc.citation.startPage865-
dc.citation.endPage868-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusEPITHELIAL-CELLS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusPATHOGENESIS-
dc.subject.keywordPlusMITOCHONDRIA-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthorcalcium-
dc.subject.keywordAuthorgamma-glutamyl transpeptidase-
dc.subject.keywordAuthorHelicobacter pylori-
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