The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.joen.2017.08.010 http://hdl.handle.net/11449/179275 |
Resumo: | Introduction This study evaluated the biocompatibility of 5 and 10 μg/mL LL-37 in vitro and its effect on the differentiation of human dental pulp stem cells (DPSCs) into odontoblast-like cells. Methods Cell viability, genotoxicity, nitric oxide production, cell cycle, dentine sialophosphoprotein (DSPP) production, and DSPP gene expression. Results Concentrations of 5 and 10 μg/mL of LL-37 were not cytotoxic and generally increased cell viability, especially on the third day (P <.05). The tested concentrations did not induce genotoxicity (P <.05). LL-37 did not significantly alter nitrite production at either concentration. Cell cycle analysis revealed that 10 μg/mL of LL-37 arrested cells in G0/G1 (P <.05). The control group exhibited higher numbers of cells in other phases of the cell cycle (P <.05). The expression of the DSPP protein and gene was also higher in the 10 μg/mL of LL-37 group (P <.05). Conclusions These results demonstrated that LL-37 was biocompatible at these concentrations and increased the number of viable cells, especially during the initial period. The 10 μg/mL concentration arrested the cell cycle and increased expression of the DSPP protein and gene, which indicates that this peptide contributes to odontoblastic differentiation. |
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The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem CellsAntimicrobial peptidebiocompatibilitydental pulpdifferentiationLL-37stem cellsIntroduction This study evaluated the biocompatibility of 5 and 10 μg/mL LL-37 in vitro and its effect on the differentiation of human dental pulp stem cells (DPSCs) into odontoblast-like cells. Methods Cell viability, genotoxicity, nitric oxide production, cell cycle, dentine sialophosphoprotein (DSPP) production, and DSPP gene expression. Results Concentrations of 5 and 10 μg/mL of LL-37 were not cytotoxic and generally increased cell viability, especially on the third day (P <.05). The tested concentrations did not induce genotoxicity (P <.05). LL-37 did not significantly alter nitrite production at either concentration. Cell cycle analysis revealed that 10 μg/mL of LL-37 arrested cells in G0/G1 (P <.05). The control group exhibited higher numbers of cells in other phases of the cell cycle (P <.05). The expression of the DSPP protein and gene was also higher in the 10 μg/mL of LL-37 group (P <.05). Conclusions These results demonstrated that LL-37 was biocompatible at these concentrations and increased the number of viable cells, especially during the initial period. The 10 μg/mL concentration arrested the cell cycle and increased expression of the DSPP protein and gene, which indicates that this peptide contributes to odontoblastic differentiation.Department of Biosciences and Oral Diagnosis São Paulo State University (UNESP) Institute of Science and TechnologyDepartment of Restorative Dentistry São Paulo State University (UNESP) Institute of Science and TechnologyDepartment of Biosciences and Oral Diagnosis São Paulo State University (UNESP) Institute of Science and TechnologyDepartment of Restorative Dentistry São Paulo State University (UNESP) Institute of Science and TechnologyUniversidade Estadual Paulista (Unesp)Milhan, Noala Vicensoto Moreira [UNESP]de Barros, Patricia Pimentel [UNESP]de Lima Zutin, Elis Andrade [UNESP]de Oliveira, Felipe Eduardo [UNESP]Camargo, Carlos Henrique Ribeiro [UNESP]Camargo, Samira Esteves Afonso [UNESP]2018-12-11T17:34:29Z2018-12-11T17:34:29Z2017-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2048-2053application/pdfhttp://dx.doi.org/10.1016/j.joen.2017.08.010Journal of Endodontics, v. 43, n. 12, p. 2048-2053, 2017.0099-2399http://hdl.handle.net/11449/17927510.1016/j.joen.2017.08.0102-s2.0-850311030182-s2.0-85031103018.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Endodontics1,585info:eu-repo/semantics/openAccess2024-01-11T06:30:33Zoai:repositorio.unesp.br:11449/179275Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:42:53.990163Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
title |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
spellingShingle |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells Milhan, Noala Vicensoto Moreira [UNESP] Antimicrobial peptide biocompatibility dental pulp differentiation LL-37 stem cells |
title_short |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
title_full |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
title_fullStr |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
title_full_unstemmed |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
title_sort |
The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells |
author |
Milhan, Noala Vicensoto Moreira [UNESP] |
author_facet |
Milhan, Noala Vicensoto Moreira [UNESP] de Barros, Patricia Pimentel [UNESP] de Lima Zutin, Elis Andrade [UNESP] de Oliveira, Felipe Eduardo [UNESP] Camargo, Carlos Henrique Ribeiro [UNESP] Camargo, Samira Esteves Afonso [UNESP] |
author_role |
author |
author2 |
de Barros, Patricia Pimentel [UNESP] de Lima Zutin, Elis Andrade [UNESP] de Oliveira, Felipe Eduardo [UNESP] Camargo, Carlos Henrique Ribeiro [UNESP] Camargo, Samira Esteves Afonso [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Milhan, Noala Vicensoto Moreira [UNESP] de Barros, Patricia Pimentel [UNESP] de Lima Zutin, Elis Andrade [UNESP] de Oliveira, Felipe Eduardo [UNESP] Camargo, Carlos Henrique Ribeiro [UNESP] Camargo, Samira Esteves Afonso [UNESP] |
dc.subject.por.fl_str_mv |
Antimicrobial peptide biocompatibility dental pulp differentiation LL-37 stem cells |
topic |
Antimicrobial peptide biocompatibility dental pulp differentiation LL-37 stem cells |
description |
Introduction This study evaluated the biocompatibility of 5 and 10 μg/mL LL-37 in vitro and its effect on the differentiation of human dental pulp stem cells (DPSCs) into odontoblast-like cells. Methods Cell viability, genotoxicity, nitric oxide production, cell cycle, dentine sialophosphoprotein (DSPP) production, and DSPP gene expression. Results Concentrations of 5 and 10 μg/mL of LL-37 were not cytotoxic and generally increased cell viability, especially on the third day (P <.05). The tested concentrations did not induce genotoxicity (P <.05). LL-37 did not significantly alter nitrite production at either concentration. Cell cycle analysis revealed that 10 μg/mL of LL-37 arrested cells in G0/G1 (P <.05). The control group exhibited higher numbers of cells in other phases of the cell cycle (P <.05). The expression of the DSPP protein and gene was also higher in the 10 μg/mL of LL-37 group (P <.05). Conclusions These results demonstrated that LL-37 was biocompatible at these concentrations and increased the number of viable cells, especially during the initial period. The 10 μg/mL concentration arrested the cell cycle and increased expression of the DSPP protein and gene, which indicates that this peptide contributes to odontoblastic differentiation. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-12-01 2018-12-11T17:34:29Z 2018-12-11T17:34:29Z |
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.2017.08.010 Journal of Endodontics, v. 43, n. 12, p. 2048-2053, 2017. 0099-2399 http://hdl.handle.net/11449/179275 10.1016/j.joen.2017.08.010 2-s2.0-85031103018 2-s2.0-85031103018.pdf |
url |
http://dx.doi.org/10.1016/j.joen.2017.08.010 http://hdl.handle.net/11449/179275 |
identifier_str_mv |
Journal of Endodontics, v. 43, n. 12, p. 2048-2053, 2017. 0099-2399 10.1016/j.joen.2017.08.010 2-s2.0-85031103018 2-s2.0-85031103018.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 |
2048-2053 application/pdf |
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 |
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1808129453822312448 |