Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis

Detalhes bibliográficos
Autor(a) principal: Chen, Ying
Data de Publicação: 2024
Outros Autores: Jiang, Zheqing, Keohane, Ana, Yang, Hu
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of applied oral science (Online)
Texto Completo: https://www.revistas.usp.br/jaos/article/view/221880
Resumo: The purpose of this study is to investigate the pathogenic role of PPARα in periodontal antigen treated gingival cells in vitro and in experimental periodontitis in vivo . Methodology: Gingival fibroblasts, gingival epithelial cells and splenocytes were isolated from C57BL/6J wild type (WT) mice and treated with fixed P. gingivalis at for 48 hours. The mRNA levels of PPARs, TNFα, IL-1β and IL-10 were detected by Real-time quantitative PCR. Silk ligatures after being soaked in the P.gingivalis suspension were tied around both maxillary second molars of WT mice or PPARα knock-out (KO) mice for two weeks. PPARα agonist fenofibrate and vehicle control were injected into the different side of the palatal gingiva on days 3, 6, and 9. At day 14, bone resorption and gingival mRNA expression levels of PPARs, TNFα, IL-1β and IL-10 were measured by micro-computed tomography and RT-qPCR respectively. Results: P. gingivalis treatment downregulated the expression of PPARα, but not PPARβ or PPARγ, and increased the expression of TNF-α and IL-1β in Gingival fibroblasts, gingival epithelial cells and splenocytes from WT mice. Gingival mRNA levels of PPARα were significantly decreased in experimental periodontitis in WT mice. The bone loss of PPARα KO mice in experimental periodontitis was significantly higher than WT mice and was not reduced by fenofibrate treatment. Gingival TNFα protein expressions were significantly increased by P. gingivalis associated ligation and decreased by fenofibrate treatment in WT mice but not in PPARα KO mice. Conclusion: This study suggests that PPARα plays an essential role in periodontitis.
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spelling Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitisPeriodontitsPeroxisome proliferator-activated receptor alphaPorphyromonas gingivalisThe purpose of this study is to investigate the pathogenic role of PPARα in periodontal antigen treated gingival cells in vitro and in experimental periodontitis in vivo . Methodology: Gingival fibroblasts, gingival epithelial cells and splenocytes were isolated from C57BL/6J wild type (WT) mice and treated with fixed P. gingivalis at for 48 hours. The mRNA levels of PPARs, TNFα, IL-1β and IL-10 were detected by Real-time quantitative PCR. Silk ligatures after being soaked in the P.gingivalis suspension were tied around both maxillary second molars of WT mice or PPARα knock-out (KO) mice for two weeks. PPARα agonist fenofibrate and vehicle control were injected into the different side of the palatal gingiva on days 3, 6, and 9. At day 14, bone resorption and gingival mRNA expression levels of PPARs, TNFα, IL-1β and IL-10 were measured by micro-computed tomography and RT-qPCR respectively. Results: P. gingivalis treatment downregulated the expression of PPARα, but not PPARβ or PPARγ, and increased the expression of TNF-α and IL-1β in Gingival fibroblasts, gingival epithelial cells and splenocytes from WT mice. Gingival mRNA levels of PPARα were significantly decreased in experimental periodontitis in WT mice. The bone loss of PPARα KO mice in experimental periodontitis was significantly higher than WT mice and was not reduced by fenofibrate treatment. Gingival TNFα protein expressions were significantly increased by P. gingivalis associated ligation and decreased by fenofibrate treatment in WT mice but not in PPARα KO mice. Conclusion: This study suggests that PPARα plays an essential role in periodontitis.Universidade de São Paulo. Faculdade de Odontologia de Bauru2024-02-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/jaos/article/view/22188010.1590/1678-7757-2023er003 Journal of Applied Oral Science; Vol. 31 (2023); 2023er003Journal of Applied Oral Science; v. 31 (2023); 2023er003Journal of Applied Oral Science; Vol. 31 (2023); 2023er0031678-77651678-7757reponame:Journal of applied oral science (Online)instname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/jaos/article/view/221880/202752Copyright (c) 2024 Journal of Applied Oral Sciencehttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessChen, Ying Jiang, ZheqingKeohane, AnaYang, Hu2024-02-08T12:05:28Zoai:revistas.usp.br:article/221880Revistahttp://www.scielo.br/jaosPUBhttps://www.revistas.usp.br/jaos/oai||jaos@usp.br1678-77651678-7757opendoar:2024-02-08T12:05:28Journal of applied oral science (Online) - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
title Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
spellingShingle Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
Chen, Ying
Periodontits
Peroxisome proliferator-activated receptor alpha
Porphyromonas gingivalis
title_short Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
title_full Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
title_fullStr Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
title_full_unstemmed Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
title_sort Erratum: In vitro and in vivo study of the pathogenic role of PPARα in experimental periodontitis
author Chen, Ying
author_facet Chen, Ying
Jiang, Zheqing
Keohane, Ana
Yang, Hu
author_role author
author2 Jiang, Zheqing
Keohane, Ana
Yang, Hu
author2_role author
author
author
dc.contributor.author.fl_str_mv Chen, Ying
Jiang, Zheqing
Keohane, Ana
Yang, Hu
dc.subject.por.fl_str_mv Periodontits
Peroxisome proliferator-activated receptor alpha
Porphyromonas gingivalis
topic Periodontits
Peroxisome proliferator-activated receptor alpha
Porphyromonas gingivalis
description The purpose of this study is to investigate the pathogenic role of PPARα in periodontal antigen treated gingival cells in vitro and in experimental periodontitis in vivo . Methodology: Gingival fibroblasts, gingival epithelial cells and splenocytes were isolated from C57BL/6J wild type (WT) mice and treated with fixed P. gingivalis at for 48 hours. The mRNA levels of PPARs, TNFα, IL-1β and IL-10 were detected by Real-time quantitative PCR. Silk ligatures after being soaked in the P.gingivalis suspension were tied around both maxillary second molars of WT mice or PPARα knock-out (KO) mice for two weeks. PPARα agonist fenofibrate and vehicle control were injected into the different side of the palatal gingiva on days 3, 6, and 9. At day 14, bone resorption and gingival mRNA expression levels of PPARs, TNFα, IL-1β and IL-10 were measured by micro-computed tomography and RT-qPCR respectively. Results: P. gingivalis treatment downregulated the expression of PPARα, but not PPARβ or PPARγ, and increased the expression of TNF-α and IL-1β in Gingival fibroblasts, gingival epithelial cells and splenocytes from WT mice. Gingival mRNA levels of PPARα were significantly decreased in experimental periodontitis in WT mice. The bone loss of PPARα KO mice in experimental periodontitis was significantly higher than WT mice and was not reduced by fenofibrate treatment. Gingival TNFα protein expressions were significantly increased by P. gingivalis associated ligation and decreased by fenofibrate treatment in WT mice but not in PPARα KO mice. Conclusion: This study suggests that PPARα plays an essential role in periodontitis.
publishDate 2024
dc.date.none.fl_str_mv 2024-02-08
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/jaos/article/view/221880
10.1590/1678-7757-2023er003
url https://www.revistas.usp.br/jaos/article/view/221880
identifier_str_mv 10.1590/1678-7757-2023er003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/jaos/article/view/221880/202752
dc.rights.driver.fl_str_mv Copyright (c) 2024 Journal of Applied Oral Science
http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2024 Journal of Applied Oral Science
http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Odontologia de Bauru
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Odontologia de Bauru
dc.source.none.fl_str_mv Journal of Applied Oral Science; Vol. 31 (2023); 2023er003
Journal of Applied Oral Science; v. 31 (2023); 2023er003
Journal of Applied Oral Science; Vol. 31 (2023); 2023er003
1678-7765
1678-7757
reponame:Journal of applied oral science (Online)
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Journal of applied oral science (Online)
collection Journal of applied oral science (Online)
repository.name.fl_str_mv Journal of applied oral science (Online) - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||jaos@usp.br
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