Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure

Detalhes bibliográficos
Autor(a) principal: Estrela, Carlos
Data de Publicação: 2016
Outros Autores: Decurcio, Daniel de Almeida, Silva, Julio Almeida, Batista, Aline Carvalho, Souza Lima, Nathalia Caroline de, Freitas Silva, Brunno Santos de, Chaves de Souza, Joao Antonio [UNESP], Souza Costa, Carlos Alberto [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.joen.2015.11.012
http://hdl.handle.net/11449/161341
Resumo: Introduction: This study assessed the immune inflammatory profile and the expression of bone resorption activators receptor activator of nuclear factor kappa B ligand (RANKL) and inhibitor osteoprotegerin (OPG) in apical periodontitis (n = 20) that persisted after root canal retreatment. Methods: Immunohistochemistry was used to characterize lymphocyte populations (CD3(+), CD45R0(+), CD8(+), and FoxP3(+) cells), macrophages (CD68(+)), RANKL(+) and OPG(+) cells in persistent apical periodontitis (PAP) and primary periapical lesions (PPLs). By using quantitative real-time polymerase chain reaction, the mRNA expression of RANKL and OPG in PAP and periodontal ligament from healthy teeth was comparatively analyzed. The data were analyzed by Mann-Whitney, Pearson chi(2), and Wilcoxon tests (5% level). Results: PAP showed an elevated number of FoxP3(+) cells compared with PPL (P < .001). The number of CD68(+) cells was reduced in the PAP samples compared with the PPLs (P < .001). Similar number of other lymphocyte populations was observed in PAP and PPLs (P > .05 for all comparisons). No differences in the RANKL, OPG, and immune-inflammatory cells were demonstrated when comparing PAP microscopically classified as cyst with those classified as granulomas (P > .05 for all comparisons). The assessment of mRNA expression revealed higher levels of RANKL. and OPG in PAP compared with the periodontal ligament from healthy teeth (contiol) samples (P < .001). Also, a greater expression of RANKL in comparison with OPG was observed in PAP (P < .001). Conclusions: These findings indicate that PAP consists of biologically active lesions that demonstrate potential of bone resorption (higher expression of RANKL) and is characterized by an immune-inflammatory cell profile that suggests a suppressive and regulatory environment (higher number of FoxP3(+) cells and lower number of macrophages) favorable to more chronic clinical behavior.
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spelling Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment FailureApical periodontitisbone resorptionimmunological cellsosteoprotegerinRANK ligandIntroduction: This study assessed the immune inflammatory profile and the expression of bone resorption activators receptor activator of nuclear factor kappa B ligand (RANKL) and inhibitor osteoprotegerin (OPG) in apical periodontitis (n = 20) that persisted after root canal retreatment. Methods: Immunohistochemistry was used to characterize lymphocyte populations (CD3(+), CD45R0(+), CD8(+), and FoxP3(+) cells), macrophages (CD68(+)), RANKL(+) and OPG(+) cells in persistent apical periodontitis (PAP) and primary periapical lesions (PPLs). By using quantitative real-time polymerase chain reaction, the mRNA expression of RANKL and OPG in PAP and periodontal ligament from healthy teeth was comparatively analyzed. The data were analyzed by Mann-Whitney, Pearson chi(2), and Wilcoxon tests (5% level). Results: PAP showed an elevated number of FoxP3(+) cells compared with PPL (P < .001). The number of CD68(+) cells was reduced in the PAP samples compared with the PPLs (P < .001). Similar number of other lymphocyte populations was observed in PAP and PPLs (P > .05 for all comparisons). No differences in the RANKL, OPG, and immune-inflammatory cells were demonstrated when comparing PAP microscopically classified as cyst with those classified as granulomas (P > .05 for all comparisons). The assessment of mRNA expression revealed higher levels of RANKL. and OPG in PAP compared with the periodontal ligament from healthy teeth (contiol) samples (P < .001). Also, a greater expression of RANKL in comparison with OPG was observed in PAP (P < .001). Conclusions: These findings indicate that PAP consists of biologically active lesions that demonstrate potential of bone resorption (higher expression of RANKL) and is characterized by an immune-inflammatory cell profile that suggests a suppressive and regulatory environment (higher number of FoxP3(+) cells and lower number of macrophages) favorable to more chronic clinical behavior.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Fed Goias, Dept Stomatol Sci, BR-74605220 Goiania, Go, BrazilUniv Estadual Campinas, Sao Paulo, BrazilSao Paulo State Univ, Araraquara Sch Dent, Dept Physiol & Pathol, Sao Paulo, BrazilSao Paulo State Univ, Araraquara Sch Dent, Dept Physiol & Pathol, Sao Paulo, BrazilCNPq: 474642/2009-7CNPq: 306394/2011-1Elsevier B.V.Universidade Federal de Goiás (UFG)Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Estrela, CarlosDecurcio, Daniel de AlmeidaSilva, Julio AlmeidaBatista, Aline CarvalhoSouza Lima, Nathalia Caroline deFreitas Silva, Brunno Santos deChaves de Souza, Joao Antonio [UNESP]Souza Costa, Carlos Alberto [UNESP]2018-11-26T16:28:07Z2018-11-26T16:28:07Z2016-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article439-446application/pdfhttp://dx.doi.org/10.1016/j.joen.2015.11.012Journal Of Endodontics. New York: Elsevier Science Inc, v. 42, n. 3, p. 439-446, 2016.0099-2399http://hdl.handle.net/11449/16134110.1016/j.joen.2015.11.012WOS:000372559700015WOS000372559700015.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Endodontics1,585info:eu-repo/semantics/openAccess2024-09-27T14:04:57Zoai:repositorio.unesp.br:11449/161341Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:04:57Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
title Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
spellingShingle Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
Estrela, Carlos
Apical periodontitis
bone resorption
immunological cells
osteoprotegerin
RANK ligand
title_short Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
title_full Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
title_fullStr Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
title_full_unstemmed Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
title_sort Immune-Inflammatory Cell Profile and Receptor Activator of Nuclear Factor Kappa B Ligand/Osteoprotegerin Expression in Persistent Apical Periodontitis after Root Canal Retreatment Failure
author Estrela, Carlos
author_facet Estrela, Carlos
Decurcio, Daniel de Almeida
Silva, Julio Almeida
Batista, Aline Carvalho
Souza Lima, Nathalia Caroline de
Freitas Silva, Brunno Santos de
Chaves de Souza, Joao Antonio [UNESP]
Souza Costa, Carlos Alberto [UNESP]
author_role author
author2 Decurcio, Daniel de Almeida
Silva, Julio Almeida
Batista, Aline Carvalho
Souza Lima, Nathalia Caroline de
Freitas Silva, Brunno Santos de
Chaves de Souza, Joao Antonio [UNESP]
Souza Costa, Carlos Alberto [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Goiás (UFG)
Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Estrela, Carlos
Decurcio, Daniel de Almeida
Silva, Julio Almeida
Batista, Aline Carvalho
Souza Lima, Nathalia Caroline de
Freitas Silva, Brunno Santos de
Chaves de Souza, Joao Antonio [UNESP]
Souza Costa, Carlos Alberto [UNESP]
dc.subject.por.fl_str_mv Apical periodontitis
bone resorption
immunological cells
osteoprotegerin
RANK ligand
topic Apical periodontitis
bone resorption
immunological cells
osteoprotegerin
RANK ligand
description Introduction: This study assessed the immune inflammatory profile and the expression of bone resorption activators receptor activator of nuclear factor kappa B ligand (RANKL) and inhibitor osteoprotegerin (OPG) in apical periodontitis (n = 20) that persisted after root canal retreatment. Methods: Immunohistochemistry was used to characterize lymphocyte populations (CD3(+), CD45R0(+), CD8(+), and FoxP3(+) cells), macrophages (CD68(+)), RANKL(+) and OPG(+) cells in persistent apical periodontitis (PAP) and primary periapical lesions (PPLs). By using quantitative real-time polymerase chain reaction, the mRNA expression of RANKL and OPG in PAP and periodontal ligament from healthy teeth was comparatively analyzed. The data were analyzed by Mann-Whitney, Pearson chi(2), and Wilcoxon tests (5% level). Results: PAP showed an elevated number of FoxP3(+) cells compared with PPL (P < .001). The number of CD68(+) cells was reduced in the PAP samples compared with the PPLs (P < .001). Similar number of other lymphocyte populations was observed in PAP and PPLs (P > .05 for all comparisons). No differences in the RANKL, OPG, and immune-inflammatory cells were demonstrated when comparing PAP microscopically classified as cyst with those classified as granulomas (P > .05 for all comparisons). The assessment of mRNA expression revealed higher levels of RANKL. and OPG in PAP compared with the periodontal ligament from healthy teeth (contiol) samples (P < .001). Also, a greater expression of RANKL in comparison with OPG was observed in PAP (P < .001). Conclusions: These findings indicate that PAP consists of biologically active lesions that demonstrate potential of bone resorption (higher expression of RANKL) and is characterized by an immune-inflammatory cell profile that suggests a suppressive and regulatory environment (higher number of FoxP3(+) cells and lower number of macrophages) favorable to more chronic clinical behavior.
publishDate 2016
dc.date.none.fl_str_mv 2016-03-01
2018-11-26T16:28:07Z
2018-11-26T16:28:07Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.joen.2015.11.012
Journal Of Endodontics. New York: Elsevier Science Inc, v. 42, n. 3, p. 439-446, 2016.
0099-2399
http://hdl.handle.net/11449/161341
10.1016/j.joen.2015.11.012
WOS:000372559700015
WOS000372559700015.pdf
url http://dx.doi.org/10.1016/j.joen.2015.11.012
http://hdl.handle.net/11449/161341
identifier_str_mv Journal Of Endodontics. New York: Elsevier Science Inc, v. 42, n. 3, p. 439-446, 2016.
0099-2399
10.1016/j.joen.2015.11.012
WOS:000372559700015
WOS000372559700015.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Endodontics
1,585
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 439-446
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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