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Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/15671
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dc.contributor.authorTrindade, Soraya Castro-
dc.contributor.authorCosta, Lilia F. Moura-
dc.contributor.authorOlczak, Teresa-
dc.contributor.authorGomes Filho, Isaac Suzart-
dc.contributor.authorVale, Vera L.-
dc.contributor.authorGaldino Neto, Milton-
dc.contributor.authorAlves, Heidiane-
dc.contributor.authorCarvalho Filho, Paulo Cirino de-
dc.creatorTrindade, Soraya Castro-
dc.creatorCosta, Lilia F. Moura-
dc.creatorOlczak, Teresa-
dc.creatorGomes Filho, Isaac Suzart-
dc.creatorVale, Vera L.-
dc.creatorGaldino Neto, Milton-
dc.creatorAlves, Heidiane-
dc.creatorCarvalho Filho, Paulo Cirino de-
dc.date.accessioned2014-08-21T19:40:35Z-
dc.date.issued2012-
dc.identifier.issn0003-9969-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/15671-
dc.descriptionTexto completo: acesso restrito. p. 314–320pt_BR
dc.description.abstractObjective Modulation of cell-mediated immunity by microorganisms in periodontal diseases has been widely studied; however, the proliferative activity and/or programmed death of mononuclear cells under periodontopathogenic stimuli are not yet well understood. The aim of this study was to investigate in vitro proliferation and death of peripheral blood mononuclear cells (PBMC) upon stimulation with Porphyromonas gingivalis (Pg) antigens. Design In 19 patients with chronic periodontitis (CP) and 16 controls without periodontitis (NP) the following clinical parameters were evaluated: bleeding on probing, probing depth, and clinical attachment level. PBMC were cultured under Pg stimuli and apoptosis/necrosis and proliferation assays were carried out for 18 and 48 h, respectively. Fluorescence of labelled cells was determined using flow cytometry. Results PBMC of CP and NP subjects exhibited a lower proliferative response to Pg LPS (p < 0.05) and HmuY protein (p < 0.001) compared with non-stimulated cells. Early apoptosis was induced by Pg LPS (p < 0.01) and Pg extract (p < 0.05), whilst all antigens induced late apoptosis (Pg LPS: p < 0.001; Pg extract: p < 0.001; HmuY: p < 0.01) and necrosis (Pg LPS: p < 0.01; Pg extract: p < 0.001; HmuY: p < 0.001). Pg LPS induced higher late apoptosis than HmuY (p < 0.05). Only Pg LPS-induced necrosis tended to be higher in CP compared with NP. Conclusions The inhibitory effect of cell proliferation caused by Pg LPS and HmuY protein is not observed when these antigens comprise Pg extract. Despite induced apoptosis, some still unknown mechanism determines the inflammatory outcome in cell death stimulated by HmuY.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org/ 10.1016/j.archoralbio.2011.09.003pt_BR
dc.subjectPeriodontitispt_BR
dc.subjectApoptosispt_BR
dc.subjectCell proliferationpt_BR
dc.subjectPorphyromonas gingivalispt_BR
dc.titlePorphyromonas gingivalis antigens differently participate in the proliferation and cell death of human PBMCpt_BR
dc.title.alternativeArchives of Oral Biologypt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 57, n. 3pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (ICS)

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