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The Antimicrobial Peptide LL-37 as a Possible Adjunct for the Proliferation and Differentiation of Dental Pulp Stem Cells.
Milhan, Noala Vicensoto Moreira; de Barros, Patricia Pimentel; de Lima Zutin, Elis Andrade; de Oliveira, Felipe Eduardo; Camargo, Carlos Henrique Ribeiro; Camargo, Samira Esteves Afonso.
Afiliación
  • Milhan NVM; Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil.
  • de Barros PP; Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil.
  • de Lima Zutin EA; Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil.
  • de Oliveira FE; Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil.
  • Camargo CHR; Department of Restorative Dentistry, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil.
  • Camargo SEA; Department of Biosciences and Oral Diagnosis, São Paulo State University (UNESP), Institute of Science and Technology, São José dos Campos, São Paulo, Brazil. Electronic address: samira@ict.unesp.br.
J Endod ; 43(12): 2048-2053, 2017 Dec.
Article en En | MEDLINE | ID: mdl-29033090
ABSTRACT

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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre / Diferenciación Celular / Pulpa Dental / Proliferación Celular / Catelicidinas Límite: Humans Idioma: En Revista: J Endod Año: 2017 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre / Diferenciación Celular / Pulpa Dental / Proliferación Celular / Catelicidinas Límite: Humans Idioma: En Revista: J Endod Año: 2017 Tipo del documento: Article País de afiliación: Brasil