Association between host defence peptide IDR‐1002 and ciprofloxacin: Effects on human dental pulp cells

Author:

Martins Danilo César Mota12ORCID,da Costa Sousa Maurício Gonçalves34ORCID,Silva Poliana Amanda Oliveira1ORCID,Aguiar Lana Ribeiro3ORCID,de Andrade Rosângela Vieira3ORCID,Silva‐Carvalho Amandda Évellin5ORCID,Saldanha‐Araújo Felipe5ORCID,Franco Octávio Luiz36ORCID,Rezende Taia Maria Berto1378ORCID

Affiliation:

1. Programa de Pós‐graduação em Ciências da Saúde Universidade de Brasília Brasília Distrito Federal Brazil

2. Curso de Odontologia Universidade Católica de Brasília Brasília Distrito Federal Brazil

3. Programa de Pós‐graduação em Ciências Genômicas e Biotecnologia Universidade Católica de Brasília Brasília Distrito Federal Brazil

4. Division of Biomaterials and Biomechanics, Department of Restorative Dentistry OHSU School of Dentistry Portland Oregon USA

5. Programa de Pós‐graduação em Patologia Molecular Universidade de Brasília Brasília Distrito Federal Brazil

6. S‐Inova Biotech, Pós‐graduação em Biotecnologia Universidade Católica Dom Bosco Mato Grosso Brazil

7. Departamento de Odontologia Universidade de Brasília Brasília Distrito Federal Brazil

8. Programa de Pós‐graduação em Odontologia Universidade de Brasília Brasília Distrito Federal Brazil

Abstract

AbstractTo evaluate the effects of the association of host defence peptide IDR‐1002 and ciprofloxacin on human dental pulp cells (hDPSCs). hDPSCs were stimulated with ciprofloxacin and IDR‐1002. Cell viability (by MTT assay), migration capacity (by scratch assay), production of inflammatory and anti‐inflammatory mediators by hDPSCs (RT‐PCR) and osteogenic differentiation (alizarin red staining) were evaluated. Phenotypic profile of hDPSCs demonstrated 97% for positive marked mesenchymal stem cell. Increased pulp cell migration and proliferation were observed after 24 and 48 h of exposure to IDR‐1002 with ciprofloxacin. Mineral matrix formation by hDPSCs was observed of the association while its reduction was observed in the presence of peptide. After 24 h, the association between ciprofloxacin and IDR‐1002 significantly downregulated TNFRSF‐1, IL‐1β, IL‐8, IL‐6 and IL‐10 gene expression (p ≤ 0.0001). The association between the IDR‐1002 and ciprofloxacin showed favourable immunomodulatory potential, emerging as a promising option for pulp revascularisation processes.

Funder

Fundação de Apoio ao Desenvolvimento do Ensino, Ciência e Tecnologia do Estado de Mato Grosso do Sul

Fundação de Apoio à Pesquisa do Distrito Federal

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Wiley

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