Publication:
Induction of toll-like receptor expression by Porphyromonas gingivalis

dc.contributor.authorNawarat Wara-Aswapatien_US
dc.contributor.authorAnek Chayasadomen_US
dc.contributor.authorRudee Surariten_US
dc.contributor.authorWaranuch Pitiphaten_US
dc.contributor.authorJason A. Bochen_US
dc.contributor.authorToshiyuki Nagasawaen_US
dc.contributor.authorIsao Ishikawaen_US
dc.contributor.authorYuichi Izumien_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherHarvard School of Dental Medicineen_US
dc.contributor.otherHealth Sciences University of Hokkaidoen_US
dc.contributor.otherTokyo Women's Medical Universityen_US
dc.contributor.otherTokyo Medical and Dental Universityen_US
dc.date.accessioned2018-10-19T04:53:08Z
dc.date.available2018-10-19T04:53:08Z
dc.date.issued2013-07-01en_US
dc.description.abstractBackground: Toll-like receptors (TLRs) play pivotal roles in host immune responses and have been suggested to be involved in the development of many infectious diseases. In this study, the mRNA expression levels of TLR2, TLR4, and TLR9 and their relationship with periodontopathic bacteria in periodon-tal tissue are examined. Furthermore, the mechanism of TLR induction by Porphyromonas gingivalis is investigated in human gingival fibroblasts (HGFs). Methods: Gingival tissue and subgingival plaque samples were collected from 19 patients with chronic periodontitis (CP) and 16 control individuals without periodontitis. Gene expression levels in the tissues and in HGFs were analyzed by reverse transcription-polymerase chain reaction (RT-PCR). The numbers of periodontopathic bacteria were determined by quantitative real-time PCR. Results: The expression levels of TLR2 and TLR9 were significantly higher in the tissues of patients with CP compared to the tissues of control individuals. The mRNA levels of TLR2 and TLR9, but not TLR4, were positively correlated with the number of P. gingivalis in subgingival plaque. P. gingivalis sonicated extract, P. gingivalis lipopolysaccharide, P. gingivalis DNA, and tumor necrosis factor-a(TNF-a) could significantly upregulate the mRNA expression of TLR2 in HGFs. Furthermore, P. gingivalis-mediated TLR2 expression was suppressed by TNF-a antibody. Conclusions: This study suggests that P. gingivalis infection induces TLR2 and TLR9 upregulation in patients with CP. P. gingivalis-induced TLR2 expression in HGFs is partially dependent on TNF-a and may lead to sensitization of HGFs to bacterial components encountered in the periodontal microenvironment.en_US
dc.identifier.citationJournal of Periodontology. Vol.84, No.7 (2013), 1010-1018en_US
dc.identifier.doi10.1902/jop.2012.120362en_US
dc.identifier.issn00223492en_US
dc.identifier.other2-s2.0-84880048088en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/31675
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880048088&origin=inwarden_US
dc.subjectDentistryen_US
dc.titleInduction of toll-like receptor expression by Porphyromonas gingivalisen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84880048088&origin=inwarden_US

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