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What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?

BACKGROUND: Oral fibroblast immunological responses to bacterial stimuli are well known. However, there are few studies about pulp fibroblasts from deciduous teeth (HDPF) responses, which are important for the treatment of pulp infections in children. The aim of this study was to evaluate expression...

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Autores principales: Colombini-Ishikiriama, Bella Luna, Dionisio, Thiago Jose, Garbieri, Thais Francini, da Silva, Rafaela Alves, Machado, Maria Aparecida Andrade Moreira, de Oliveira, Sandra Helena Penha, Lara, Vanessa Soares, Greene, Andrew Seth, Santos, Carlos Ferreira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310245/
https://www.ncbi.nlm.nih.gov/pubmed/32571213
http://dx.doi.org/10.1186/s12865-020-00367-8
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author Colombini-Ishikiriama, Bella Luna
Dionisio, Thiago Jose
Garbieri, Thais Francini
da Silva, Rafaela Alves
Machado, Maria Aparecida Andrade Moreira
de Oliveira, Sandra Helena Penha
Lara, Vanessa Soares
Greene, Andrew Seth
Santos, Carlos Ferreira
author_facet Colombini-Ishikiriama, Bella Luna
Dionisio, Thiago Jose
Garbieri, Thais Francini
da Silva, Rafaela Alves
Machado, Maria Aparecida Andrade Moreira
de Oliveira, Sandra Helena Penha
Lara, Vanessa Soares
Greene, Andrew Seth
Santos, Carlos Ferreira
author_sort Colombini-Ishikiriama, Bella Luna
collection PubMed
description BACKGROUND: Oral fibroblast immunological responses to bacterial stimuli are well known. However, there are few studies about pulp fibroblasts from deciduous teeth (HDPF) responses, which are important for the treatment of pulp infections in children. The aim of this study was to evaluate expression and production of inflammatory cytokines and chemokines by HDPF when challenged with bacterial antigens normally present in advanced caries lesions. METHODS: Triplicate HDPF from 4 children (n = 4; 2 boys and 2 girls) were cultured by explant technique and challenged or not with Escherichia coli lipopolysaccharide/1 μg/mL (EcLPS) or Enterococcus faecalis lipoteichoic acid/1 μg/mL (EfLTA) for 6 and 24 h. Most of published studies employed immortalized cells, i.e., without checking possible gender and genetic variables. mRNA expression and protein production were evaluated by RT-qPCR and ELISA MILLIPLEX®, respectively, for Interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12, IL-17, Chemokine C-C motif ligand 2/monocyte chemoattractant protein 1 (CCL2/MCP-1), Chemokine C-C motif ligand 3/macrophage inflammatory protein 1-alpha (CCL3/MIP1-α), Chemokine C-C motif ligand 5/ regulated on activation, normal T cell expressed and secreted (CCL5/RANTES), C-X-C motif chemokine 12/ stromal cell-derived factor 1 (CXCL12/SDF-1), Tumor Necrosis Factor-alpha (TNF-α), Interferon-gamma (IFN γ), Vascular Endothelial Growth Factor (VEGF), Colony stimulating factor 1 (CSF-1) and Macrophage colony-stimulating factor (M-CSF). RESULTS: EcLPS increased IL-1α, IL-1β, IL-8, CCL2, CCL5, TNF-α and CSF-1 mRNA and protein levels while EfLTA was only able to positively regulate gene expression and protein production of IL-8. CONCLUSION: The results of the present study confirmed our hypothesis, since pulp fibroblasts from deciduous teeth are capable of increasing gene expression and protein production after being stimulated with EcLPS and EfLTA.
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spelling pubmed-73102452020-06-23 What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA? Colombini-Ishikiriama, Bella Luna Dionisio, Thiago Jose Garbieri, Thais Francini da Silva, Rafaela Alves Machado, Maria Aparecida Andrade Moreira de Oliveira, Sandra Helena Penha Lara, Vanessa Soares Greene, Andrew Seth Santos, Carlos Ferreira BMC Immunol Research Article BACKGROUND: Oral fibroblast immunological responses to bacterial stimuli are well known. However, there are few studies about pulp fibroblasts from deciduous teeth (HDPF) responses, which are important for the treatment of pulp infections in children. The aim of this study was to evaluate expression and production of inflammatory cytokines and chemokines by HDPF when challenged with bacterial antigens normally present in advanced caries lesions. METHODS: Triplicate HDPF from 4 children (n = 4; 2 boys and 2 girls) were cultured by explant technique and challenged or not with Escherichia coli lipopolysaccharide/1 μg/mL (EcLPS) or Enterococcus faecalis lipoteichoic acid/1 μg/mL (EfLTA) for 6 and 24 h. Most of published studies employed immortalized cells, i.e., without checking possible gender and genetic variables. mRNA expression and protein production were evaluated by RT-qPCR and ELISA MILLIPLEX®, respectively, for Interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12, IL-17, Chemokine C-C motif ligand 2/monocyte chemoattractant protein 1 (CCL2/MCP-1), Chemokine C-C motif ligand 3/macrophage inflammatory protein 1-alpha (CCL3/MIP1-α), Chemokine C-C motif ligand 5/ regulated on activation, normal T cell expressed and secreted (CCL5/RANTES), C-X-C motif chemokine 12/ stromal cell-derived factor 1 (CXCL12/SDF-1), Tumor Necrosis Factor-alpha (TNF-α), Interferon-gamma (IFN γ), Vascular Endothelial Growth Factor (VEGF), Colony stimulating factor 1 (CSF-1) and Macrophage colony-stimulating factor (M-CSF). RESULTS: EcLPS increased IL-1α, IL-1β, IL-8, CCL2, CCL5, TNF-α and CSF-1 mRNA and protein levels while EfLTA was only able to positively regulate gene expression and protein production of IL-8. CONCLUSION: The results of the present study confirmed our hypothesis, since pulp fibroblasts from deciduous teeth are capable of increasing gene expression and protein production after being stimulated with EcLPS and EfLTA. BioMed Central 2020-06-22 /pmc/articles/PMC7310245/ /pubmed/32571213 http://dx.doi.org/10.1186/s12865-020-00367-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Colombini-Ishikiriama, Bella Luna
Dionisio, Thiago Jose
Garbieri, Thais Francini
da Silva, Rafaela Alves
Machado, Maria Aparecida Andrade Moreira
de Oliveira, Sandra Helena Penha
Lara, Vanessa Soares
Greene, Andrew Seth
Santos, Carlos Ferreira
What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title_full What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title_fullStr What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title_full_unstemmed What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title_short What is the response profile of deciduous pulp fibroblasts stimulated with E. coli LPS and E. faecalis LTA?
title_sort what is the response profile of deciduous pulp fibroblasts stimulated with e. coli lps and e. faecalis lta?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310245/
https://www.ncbi.nlm.nih.gov/pubmed/32571213
http://dx.doi.org/10.1186/s12865-020-00367-8
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