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Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation

Cariogenic Streptococcus mutans (S. mutans) is implicated in the dental pulp necrosis but also in cardiovascular tissue infections. Herein, the purpose was to elucidate how human dental pulp derived stromal cells (DPSCs) react toward a direct interaction with S. mutans. DPSCs were challenged with S....

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Autores principales: Maisonneuve, Elodie, Chevrier, Julie, Dubus, Marie, Varin, Jennifer, Sergheraert, Johan, Gangloff, Sophie C., Reffuveille, Fany, Mauprivez, Cédric, Kerdjoudj, Halima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487799/
https://www.ncbi.nlm.nih.gov/pubmed/32984312
http://dx.doi.org/10.3389/fcell.2020.00785
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author Maisonneuve, Elodie
Chevrier, Julie
Dubus, Marie
Varin, Jennifer
Sergheraert, Johan
Gangloff, Sophie C.
Reffuveille, Fany
Mauprivez, Cédric
Kerdjoudj, Halima
author_facet Maisonneuve, Elodie
Chevrier, Julie
Dubus, Marie
Varin, Jennifer
Sergheraert, Johan
Gangloff, Sophie C.
Reffuveille, Fany
Mauprivez, Cédric
Kerdjoudj, Halima
author_sort Maisonneuve, Elodie
collection PubMed
description Cariogenic Streptococcus mutans (S. mutans) is implicated in the dental pulp necrosis but also in cardiovascular tissue infections. Herein, the purpose was to elucidate how human dental pulp derived stromal cells (DPSCs) react toward a direct interaction with S. mutans. DPSCs were challenged with S. mutans. Following 3 h of interaction, DPSCs were able to internalize S. mutans (rate < 1%), and F-actin fibers played a significant role in this process. S. mutans persisted in the DPSCs for 48 h without causing a cytotoxic effect. S. mutans was, however, able to get out of the DPSCs cytoplasm and to proliferate in the extracellular environment. Yet, we noticed several adaptive responses of bacteria to the extracellular environment such as a modification of the kinetic growth, the increase in biofilm formation on type I collagen and polyester fabrics, as well as a tolerance toward amoxicillin. In response to infection, DPSCs adopted a proinflammatory profile by increasing the secretion of IL-8, lL-1β, and TNF-α, strengthening the establishment of the dental pulp inflammation. Overall, these findings showed a direct impact of S. mutans on DPSCs, providing new insights into the potential role of S. mutans in infective diseases.
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spelling pubmed-74877992020-09-25 Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation Maisonneuve, Elodie Chevrier, Julie Dubus, Marie Varin, Jennifer Sergheraert, Johan Gangloff, Sophie C. Reffuveille, Fany Mauprivez, Cédric Kerdjoudj, Halima Front Cell Dev Biol Cell and Developmental Biology Cariogenic Streptococcus mutans (S. mutans) is implicated in the dental pulp necrosis but also in cardiovascular tissue infections. Herein, the purpose was to elucidate how human dental pulp derived stromal cells (DPSCs) react toward a direct interaction with S. mutans. DPSCs were challenged with S. mutans. Following 3 h of interaction, DPSCs were able to internalize S. mutans (rate < 1%), and F-actin fibers played a significant role in this process. S. mutans persisted in the DPSCs for 48 h without causing a cytotoxic effect. S. mutans was, however, able to get out of the DPSCs cytoplasm and to proliferate in the extracellular environment. Yet, we noticed several adaptive responses of bacteria to the extracellular environment such as a modification of the kinetic growth, the increase in biofilm formation on type I collagen and polyester fabrics, as well as a tolerance toward amoxicillin. In response to infection, DPSCs adopted a proinflammatory profile by increasing the secretion of IL-8, lL-1β, and TNF-α, strengthening the establishment of the dental pulp inflammation. Overall, these findings showed a direct impact of S. mutans on DPSCs, providing new insights into the potential role of S. mutans in infective diseases. Frontiers Media S.A. 2020-08-31 /pmc/articles/PMC7487799/ /pubmed/32984312 http://dx.doi.org/10.3389/fcell.2020.00785 Text en Copyright © 2020 Maisonneuve, Chevrier, Dubus, Varin, Sergheraert, Gangloff, Reffuveille, Mauprivez and Kerdjoudj. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Maisonneuve, Elodie
Chevrier, Julie
Dubus, Marie
Varin, Jennifer
Sergheraert, Johan
Gangloff, Sophie C.
Reffuveille, Fany
Mauprivez, Cédric
Kerdjoudj, Halima
Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title_full Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title_fullStr Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title_full_unstemmed Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title_short Infection of Human Dental Pulp Stromal Cells by Streptococcus mutans: Shedding Light on Bacteria Pathogenicity and Pulp Inflammation
title_sort infection of human dental pulp stromal cells by streptococcus mutans: shedding light on bacteria pathogenicity and pulp inflammation
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487799/
https://www.ncbi.nlm.nih.gov/pubmed/32984312
http://dx.doi.org/10.3389/fcell.2020.00785
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