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dc.contributor.authorP. Montreekachonen_US
dc.contributor.authorP. Chotjumlongen_US
dc.contributor.authorV. Reutrakulen_US
dc.contributor.authorS. Krisanaprakornkiten_US
dc.date.accessioned2018-09-10T03:16:38Z-
dc.date.available2018-09-10T03:16:38Z-
dc.date.issued2009-11-01en_US
dc.identifier.issn15440591en_US
dc.identifier.issn00220345en_US
dc.identifier.other2-s2.0-70350422757en_US
dc.identifier.other10.1177/0022034509345967en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70350422757&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/59521-
dc.description.abstractMatrix metalloproteinase-9 (MMP-9) is important in the pathogenesis of periodontitis. Cytosolic phospholipase A22α (cPLA22α) is involved in MMP-9 up-regulation in human monocytes. We tested the hypothesis that cPLA22α also regulates MMP-9 induction by Fusobacterium nucleatum and by phorbol 12-myristate-13-acetate (PMA) in gingival epithelial cells. While PMA induced MMP-9 expression considerably, F. nucleatum did so moderately. This time-course study demonstrated that MMP-9 mRNA up-regulation occurred at 3 hours, whereas MMP-9 secretion and activity in cell-free supernatants occurred at 12 hours. cPLA2α mRNA was constitutively expressed in gingival epithelial cells. Transient activation of cPLA2by Ser505 phosphorylation was observed in the nuclei upon stimulation, suggesting its role as a transcription factor, while cPLA2protein expression remained unchanged. Induction of MMP-9 expression and activity was significantly inhibited by 1 1/4M of the specific cPLA2α inhibitor (P < 0.01). These findings demonstrate the involvement of cPLA2α in MMP-9 up-regulation.en_US
dc.subjectDentistryen_US
dc.titleInvolvement of cytosolic phospholipase A2α in MMP-9 Up-regulationen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Dental Researchen_US
article.volume88en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMahidol Universityen_US
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