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Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures

The human vaginal microbiome plays a critical but poorly defined role in reproductive health. Vaginal microbiome alterations are associated with increased susceptibility to sexually-transmitted infections (STI) possibly due to related changes in innate defense responses from epithelial cells. Study...

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Detalles Bibliográficos
Autores principales: Rose, William A., McGowin, Chris L., Spagnuolo, Rae Ann, Eaves-Pyles, Tonyia D., Popov, Vsevolod L., Pyles, Richard B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296736/
https://www.ncbi.nlm.nih.gov/pubmed/22412914
http://dx.doi.org/10.1371/journal.pone.0032728
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author Rose, William A.
McGowin, Chris L.
Spagnuolo, Rae Ann
Eaves-Pyles, Tonyia D.
Popov, Vsevolod L.
Pyles, Richard B.
author_facet Rose, William A.
McGowin, Chris L.
Spagnuolo, Rae Ann
Eaves-Pyles, Tonyia D.
Popov, Vsevolod L.
Pyles, Richard B.
author_sort Rose, William A.
collection PubMed
description The human vaginal microbiome plays a critical but poorly defined role in reproductive health. Vaginal microbiome alterations are associated with increased susceptibility to sexually-transmitted infections (STI) possibly due to related changes in innate defense responses from epithelial cells. Study of the impact of commensal bacteria on the vaginal mucosal surface has been hindered by current vaginal epithelial cell (VEC) culture systems that lack an appropriate interface between the apical surface of stratified squamous epithelium and the air-filled vaginal lumen. Therefore we developed a reproducible multilayer VEC culture system with an apical (luminal) air-interface that supported colonization with selected commensal bacteria. Multilayer VEC developed tight-junctions and other hallmarks of the vaginal mucosa including predictable proinflammatory cytokine secretion following TLR stimulation. Colonization of multilayers by common vaginal commensals including Lactobacillus crispatus, L. jensenii, and L. rhamnosus led to intimate associations with the VEC exclusively on the apical surface. Vaginal commensals did not trigger cytokine secretion but Staphylococcus epidermidis, a skin commensal, was inflammatory. Lactobacilli reduced cytokine secretion in an isolate-specific fashion following TLR stimulation. This tempering of inflammation offers a potential explanation for increased susceptibility to STI in the absence of common commensals and has implications for testing of potential STI preventatives.
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spelling pubmed-32967362012-03-12 Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures Rose, William A. McGowin, Chris L. Spagnuolo, Rae Ann Eaves-Pyles, Tonyia D. Popov, Vsevolod L. Pyles, Richard B. PLoS One Research Article The human vaginal microbiome plays a critical but poorly defined role in reproductive health. Vaginal microbiome alterations are associated with increased susceptibility to sexually-transmitted infections (STI) possibly due to related changes in innate defense responses from epithelial cells. Study of the impact of commensal bacteria on the vaginal mucosal surface has been hindered by current vaginal epithelial cell (VEC) culture systems that lack an appropriate interface between the apical surface of stratified squamous epithelium and the air-filled vaginal lumen. Therefore we developed a reproducible multilayer VEC culture system with an apical (luminal) air-interface that supported colonization with selected commensal bacteria. Multilayer VEC developed tight-junctions and other hallmarks of the vaginal mucosa including predictable proinflammatory cytokine secretion following TLR stimulation. Colonization of multilayers by common vaginal commensals including Lactobacillus crispatus, L. jensenii, and L. rhamnosus led to intimate associations with the VEC exclusively on the apical surface. Vaginal commensals did not trigger cytokine secretion but Staphylococcus epidermidis, a skin commensal, was inflammatory. Lactobacilli reduced cytokine secretion in an isolate-specific fashion following TLR stimulation. This tempering of inflammation offers a potential explanation for increased susceptibility to STI in the absence of common commensals and has implications for testing of potential STI preventatives. Public Library of Science 2012-03-07 /pmc/articles/PMC3296736/ /pubmed/22412914 http://dx.doi.org/10.1371/journal.pone.0032728 Text en Rose et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rose, William A.
McGowin, Chris L.
Spagnuolo, Rae Ann
Eaves-Pyles, Tonyia D.
Popov, Vsevolod L.
Pyles, Richard B.
Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title_full Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title_fullStr Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title_full_unstemmed Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title_short Commensal Bacteria Modulate Innate Immune Responses of Vaginal Epithelial Cell Multilayer Cultures
title_sort commensal bacteria modulate innate immune responses of vaginal epithelial cell multilayer cultures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296736/
https://www.ncbi.nlm.nih.gov/pubmed/22412914
http://dx.doi.org/10.1371/journal.pone.0032728
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