Acquired pellicle protein-based engineering protects against erosive demineralization
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.jdent.2020.103478 http://hdl.handle.net/11449/206608 |
Resumo: | Objectives: To evaluate, in vivo: 1) proteomic alterations in the acquired enamel pellicle (AEP) after treatment with sugarcane-derived cystatin (CaneCPI-5), hemoglobin (HB), statherin-derived peptide (StN15) or their combination before the formation of the AEP and subsequent erosive challenge; 2) the protection of these treatments against erosive demnineralization. Materials and methods: In 5 crossover phases, after prophylaxis, 10 volunteers rinsed (10 mL, 1 min) with: deionized water-1, 0.1 mg/mL CaneCPI-5-2, 1.0 mg/mL HB-3, 1.88 × 10-5 M StN15-4 or their combination-5. AEP was formed (2 h) and enamel biopsy (10 μL, 1%citric acid, pH 2.5, 10 s) was performed on one incisor for calcium analysis. The same acid was applied on the vestibular surfaces of the remaining teeth. The acid-resistant proteins within the remaining AEP were collected. Samples were quantitatively analyzed by label-free proteomics. Results: Treatment with the proteins/peptide, isolated or combined, increased several acid-resistant proteins in the AEP, compared with control. The highest increases were seen for PRPs (32-fold, StN15), profilin (15-fold, combination), alpha-amylase (9-fold; StN15), keratins (8-fold, CaneCPI-5 and HB), Histatin-1 (7-fold, StN15), immunoglobulins (6.5-fold, StN15), lactotransferrin (4-fold, CaneCPI-5), cystatins, lysozyme, protein S-100-A9 and actins (3.5-fold, StN15), serum albumin (3.5-fold, CaneCPI-5 and HB) and hemoglobin (3-fold, StN15). Annexin, calmodulin, keratin, tubulin and cystatins were identified exclusively upon treatment with the proteins/peptide, alone or combined. Groups 2, 3 and 4 had significantly lower Ca released from enamel compared to group 1 (Kruskal-Wallis/Dunn's, p < 0.05). Conclusions: Treatment with CaneCPI-5, HB or StN15 remarkably increases acid-resistant proteins in the AEP, protecting against erosion. Clinical significance: Our results show, for the first time, that treatment with proteins/peptide remarkably increases acid-resistant proteins in the AEP, protecting against erosive demineralization. These findings open an avenue for a new preventive approach for erosive demineralization, employing acquired pellicle engineering procedures that may in the future be incorporated into dental products. |
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Acquired pellicle protein-based engineering protects against erosive demineralizationAcquired enamel pellicleCystatinDental erosionHemoglobinProteomicsStatherinObjectives: To evaluate, in vivo: 1) proteomic alterations in the acquired enamel pellicle (AEP) after treatment with sugarcane-derived cystatin (CaneCPI-5), hemoglobin (HB), statherin-derived peptide (StN15) or their combination before the formation of the AEP and subsequent erosive challenge; 2) the protection of these treatments against erosive demnineralization. Materials and methods: In 5 crossover phases, after prophylaxis, 10 volunteers rinsed (10 mL, 1 min) with: deionized water-1, 0.1 mg/mL CaneCPI-5-2, 1.0 mg/mL HB-3, 1.88 × 10-5 M StN15-4 or their combination-5. AEP was formed (2 h) and enamel biopsy (10 μL, 1%citric acid, pH 2.5, 10 s) was performed on one incisor for calcium analysis. The same acid was applied on the vestibular surfaces of the remaining teeth. The acid-resistant proteins within the remaining AEP were collected. Samples were quantitatively analyzed by label-free proteomics. Results: Treatment with the proteins/peptide, isolated or combined, increased several acid-resistant proteins in the AEP, compared with control. The highest increases were seen for PRPs (32-fold, StN15), profilin (15-fold, combination), alpha-amylase (9-fold; StN15), keratins (8-fold, CaneCPI-5 and HB), Histatin-1 (7-fold, StN15), immunoglobulins (6.5-fold, StN15), lactotransferrin (4-fold, CaneCPI-5), cystatins, lysozyme, protein S-100-A9 and actins (3.5-fold, StN15), serum albumin (3.5-fold, CaneCPI-5 and HB) and hemoglobin (3-fold, StN15). Annexin, calmodulin, keratin, tubulin and cystatins were identified exclusively upon treatment with the proteins/peptide, alone or combined. Groups 2, 3 and 4 had significantly lower Ca released from enamel compared to group 1 (Kruskal-Wallis/Dunn's, p < 0.05). Conclusions: Treatment with CaneCPI-5, HB or StN15 remarkably increases acid-resistant proteins in the AEP, protecting against erosion. Clinical significance: Our results show, for the first time, that treatment with proteins/peptide remarkably increases acid-resistant proteins in the AEP, protecting against erosive demineralization. These findings open an avenue for a new preventive approach for erosive demineralization, employing acquired pellicle engineering procedures that may in the future be incorporated into dental products.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Department of Biological Sciences Bauru School of Dentistry University of São PauloDepartment of Biochemistry and Technology Institute of Chemistry São Paulo State University (UNESP)Department of Genetics and Evolution São Carlos Federal UniversityDepartment of Preventive and Restorative Dentistry School of Dentistry Araçatuba São Paulo State University (UNESP)Department of Biochemistry and Technology Institute of Chemistry São Paulo State University (UNESP)Department of Preventive and Restorative Dentistry School of Dentistry Araçatuba São Paulo State University (UNESP)FAPESP: 2018/12041-7FAPESP: 2019/16254-8CNPq: 407853/2018-9Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)São Carlos Federal UniversityCarvalho, Thamyris SouzaAraújo, Tamara TeodoroVentura, Talita Mendes OliveiraDionizio, AlineCâmara, João Victor FrazãoMoraes, Samanta MascarenhasPelá, Vinicius TaioquiMartini, TatianaLeme, Julia ChaparroDerbotolli, Ana Luiza BogazGrizzo, Larissa TerciliaCrusca, Edson [UNESP]Shibao, Priscila Yumi TanakaMarchetto, Reinaldo [UNESP]Henrique-Silva, FlavioPessan, Juliano Pelim [UNESP]Buzalaf, Marília Afonso Rabelo2021-06-25T10:35:09Z2021-06-25T10:35:09Z2020-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.jdent.2020.103478Journal of Dentistry, v. 102.0300-5712http://hdl.handle.net/11449/20660810.1016/j.jdent.2020.1034782-s2.0-85092044048Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Dentistryinfo:eu-repo/semantics/openAccess2024-09-19T18:31:44Zoai:repositorio.unesp.br:11449/206608Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T18:31:44Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Acquired pellicle protein-based engineering protects against erosive demineralization |
title |
Acquired pellicle protein-based engineering protects against erosive demineralization |
spellingShingle |
Acquired pellicle protein-based engineering protects against erosive demineralization Carvalho, Thamyris Souza Acquired enamel pellicle Cystatin Dental erosion Hemoglobin Proteomics Statherin |
title_short |
Acquired pellicle protein-based engineering protects against erosive demineralization |
title_full |
Acquired pellicle protein-based engineering protects against erosive demineralization |
title_fullStr |
Acquired pellicle protein-based engineering protects against erosive demineralization |
title_full_unstemmed |
Acquired pellicle protein-based engineering protects against erosive demineralization |
title_sort |
Acquired pellicle protein-based engineering protects against erosive demineralization |
author |
Carvalho, Thamyris Souza |
author_facet |
Carvalho, Thamyris Souza Araújo, Tamara Teodoro Ventura, Talita Mendes Oliveira Dionizio, Aline Câmara, João Victor Frazão Moraes, Samanta Mascarenhas Pelá, Vinicius Taioqui Martini, Tatiana Leme, Julia Chaparro Derbotolli, Ana Luiza Bogaz Grizzo, Larissa Tercilia Crusca, Edson [UNESP] Shibao, Priscila Yumi Tanaka Marchetto, Reinaldo [UNESP] Henrique-Silva, Flavio Pessan, Juliano Pelim [UNESP] Buzalaf, Marília Afonso Rabelo |
author_role |
author |
author2 |
Araújo, Tamara Teodoro Ventura, Talita Mendes Oliveira Dionizio, Aline Câmara, João Victor Frazão Moraes, Samanta Mascarenhas Pelá, Vinicius Taioqui Martini, Tatiana Leme, Julia Chaparro Derbotolli, Ana Luiza Bogaz Grizzo, Larissa Tercilia Crusca, Edson [UNESP] Shibao, Priscila Yumi Tanaka Marchetto, Reinaldo [UNESP] Henrique-Silva, Flavio Pessan, Juliano Pelim [UNESP] Buzalaf, Marília Afonso Rabelo |
author2_role |
author author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) São Carlos Federal University |
dc.contributor.author.fl_str_mv |
Carvalho, Thamyris Souza Araújo, Tamara Teodoro Ventura, Talita Mendes Oliveira Dionizio, Aline Câmara, João Victor Frazão Moraes, Samanta Mascarenhas Pelá, Vinicius Taioqui Martini, Tatiana Leme, Julia Chaparro Derbotolli, Ana Luiza Bogaz Grizzo, Larissa Tercilia Crusca, Edson [UNESP] Shibao, Priscila Yumi Tanaka Marchetto, Reinaldo [UNESP] Henrique-Silva, Flavio Pessan, Juliano Pelim [UNESP] Buzalaf, Marília Afonso Rabelo |
dc.subject.por.fl_str_mv |
Acquired enamel pellicle Cystatin Dental erosion Hemoglobin Proteomics Statherin |
topic |
Acquired enamel pellicle Cystatin Dental erosion Hemoglobin Proteomics Statherin |
description |
Objectives: To evaluate, in vivo: 1) proteomic alterations in the acquired enamel pellicle (AEP) after treatment with sugarcane-derived cystatin (CaneCPI-5), hemoglobin (HB), statherin-derived peptide (StN15) or their combination before the formation of the AEP and subsequent erosive challenge; 2) the protection of these treatments against erosive demnineralization. Materials and methods: In 5 crossover phases, after prophylaxis, 10 volunteers rinsed (10 mL, 1 min) with: deionized water-1, 0.1 mg/mL CaneCPI-5-2, 1.0 mg/mL HB-3, 1.88 × 10-5 M StN15-4 or their combination-5. AEP was formed (2 h) and enamel biopsy (10 μL, 1%citric acid, pH 2.5, 10 s) was performed on one incisor for calcium analysis. The same acid was applied on the vestibular surfaces of the remaining teeth. The acid-resistant proteins within the remaining AEP were collected. Samples were quantitatively analyzed by label-free proteomics. Results: Treatment with the proteins/peptide, isolated or combined, increased several acid-resistant proteins in the AEP, compared with control. The highest increases were seen for PRPs (32-fold, StN15), profilin (15-fold, combination), alpha-amylase (9-fold; StN15), keratins (8-fold, CaneCPI-5 and HB), Histatin-1 (7-fold, StN15), immunoglobulins (6.5-fold, StN15), lactotransferrin (4-fold, CaneCPI-5), cystatins, lysozyme, protein S-100-A9 and actins (3.5-fold, StN15), serum albumin (3.5-fold, CaneCPI-5 and HB) and hemoglobin (3-fold, StN15). Annexin, calmodulin, keratin, tubulin and cystatins were identified exclusively upon treatment with the proteins/peptide, alone or combined. Groups 2, 3 and 4 had significantly lower Ca released from enamel compared to group 1 (Kruskal-Wallis/Dunn's, p < 0.05). Conclusions: Treatment with CaneCPI-5, HB or StN15 remarkably increases acid-resistant proteins in the AEP, protecting against erosion. Clinical significance: Our results show, for the first time, that treatment with proteins/peptide remarkably increases acid-resistant proteins in the AEP, protecting against erosive demineralization. These findings open an avenue for a new preventive approach for erosive demineralization, employing acquired pellicle engineering procedures that may in the future be incorporated into dental products. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-11-01 2021-06-25T10:35:09Z 2021-06-25T10:35:09Z |
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.jdent.2020.103478 Journal of Dentistry, v. 102. 0300-5712 http://hdl.handle.net/11449/206608 10.1016/j.jdent.2020.103478 2-s2.0-85092044048 |
url |
http://dx.doi.org/10.1016/j.jdent.2020.103478 http://hdl.handle.net/11449/206608 |
identifier_str_mv |
Journal of Dentistry, v. 102. 0300-5712 10.1016/j.jdent.2020.103478 2-s2.0-85092044048 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Dentistry |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus 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 |
_version_ |
1813546468042080256 |