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Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells

The recognition of bacterial components on the intestinal epithelial cells occurs through the toll-like receptors and is followed by the induction of an effective innate immune response. We analyzed receptor expression and signaling pathways involved in activation of human colon adenocarcinoma cells...

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Detalles Bibliográficos
Autores principales: Elena, Grimaldi, Giovanna, Donnarumma, Brunella, Perfetto, De Anna, Filippis, Alessandro, Melito, Antonietta, Tufano Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768557/
https://www.ncbi.nlm.nih.gov/pubmed/24031417
http://dx.doi.org/10.1590/S1517-838220090003000036
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author Elena, Grimaldi
Giovanna, Donnarumma
Brunella, Perfetto
De Anna, Filippis
Alessandro, Melito
Antonietta, Tufano Maria
author_facet Elena, Grimaldi
Giovanna, Donnarumma
Brunella, Perfetto
De Anna, Filippis
Alessandro, Melito
Antonietta, Tufano Maria
author_sort Elena, Grimaldi
collection PubMed
description The recognition of bacterial components on the intestinal epithelial cells occurs through the toll-like receptors and is followed by the induction of an effective innate immune response. We analyzed receptor expression and signaling pathways involved in activation of human colon adenocarcinoma cells after stimulation with porins and LPS of Shigella flexneri. We also analyzed the expression and production of some cytokines, of intercellular adhesion molecule-1, of antimicrobial peptides human β-defensins, and of the inducible form of nitric oxide synthase. Our data demonstrate that TLR2 is involved in porin recognition, whereas TLR4 with MD2, is required for LPS recognition.
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spelling pubmed-37685572013-09-12 Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells Elena, Grimaldi Giovanna, Donnarumma Brunella, Perfetto De Anna, Filippis Alessandro, Melito Antonietta, Tufano Maria Braz J Microbiol Medical Microbiology The recognition of bacterial components on the intestinal epithelial cells occurs through the toll-like receptors and is followed by the induction of an effective innate immune response. We analyzed receptor expression and signaling pathways involved in activation of human colon adenocarcinoma cells after stimulation with porins and LPS of Shigella flexneri. We also analyzed the expression and production of some cytokines, of intercellular adhesion molecule-1, of antimicrobial peptides human β-defensins, and of the inducible form of nitric oxide synthase. Our data demonstrate that TLR2 is involved in porin recognition, whereas TLR4 with MD2, is required for LPS recognition. Sociedade Brasileira de Microbiologia 2009 2009-09-01 /pmc/articles/PMC3768557/ /pubmed/24031417 http://dx.doi.org/10.1590/S1517-838220090003000036 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Medical Microbiology
Elena, Grimaldi
Giovanna, Donnarumma
Brunella, Perfetto
De Anna, Filippis
Alessandro, Melito
Antonietta, Tufano Maria
Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title_full Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title_fullStr Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title_full_unstemmed Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title_short Proinflammatory signal transduction pathway induced by Shigella flexneri porins in caco-2 cells
title_sort proinflammatory signal transduction pathway induced by shigella flexneri porins in caco-2 cells
topic Medical Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768557/
https://www.ncbi.nlm.nih.gov/pubmed/24031417
http://dx.doi.org/10.1590/S1517-838220090003000036
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