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Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis

BACKGROUND: The aim of this study is to evaluate the role of NADPH oxidase in primary intestinal epithelial cells during the active phase of UC. METHODS: The primary human colonic epithelial cells were isolated from 19 patients with mild to moderate inflammatory activity of UC and 14 controls using...

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Autores principales: Ramonaite, Rima, Skieceviciene, Jurgita, Kiudelis, Gediminas, Jonaitis, Laimas, Tamelis, Algimantas, Cizas, Paulius, Borutaite, Vilmante, Kupcinskas, Limas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834533/
https://www.ncbi.nlm.nih.gov/pubmed/24229374
http://dx.doi.org/10.1186/1471-230X-13-159
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author Ramonaite, Rima
Skieceviciene, Jurgita
Kiudelis, Gediminas
Jonaitis, Laimas
Tamelis, Algimantas
Cizas, Paulius
Borutaite, Vilmante
Kupcinskas, Limas
author_facet Ramonaite, Rima
Skieceviciene, Jurgita
Kiudelis, Gediminas
Jonaitis, Laimas
Tamelis, Algimantas
Cizas, Paulius
Borutaite, Vilmante
Kupcinskas, Limas
author_sort Ramonaite, Rima
collection PubMed
description BACKGROUND: The aim of this study is to evaluate the role of NADPH oxidase in primary intestinal epithelial cells during the active phase of UC. METHODS: The primary human colonic epithelial cells were isolated from 19 patients with mild to moderate inflammatory activity of UC and 14 controls using chelation method. The cells were cultivated under the effect of mediators. Viability of cells was assessed by fluorescent microscopy. Production of reactive oxygen species (ROS) by the cells was measured fluorimetrically using Amplex Red. Production of TNF-α cytokine by the colonic epithelial cells was analysed by ELISA. RESULTS: The results of our study showed that unstimulated cells of UC patients had a decreased viability, increased ROS production, but similar TNF-α level when compared to the controls. Stimulation with LPS increased hydrogen peroxide and TNF-α level in the UC group. Treatment of colonic epithelial cells with NADPH oxidase inhibitor increased cell viability decreased the levels of ROS and TNF-α in the LPS-treated cells isolated from UC patients. CONCLUSIONS: Our study showed that bacterial endotoxins induced NADPH oxidase activation in the colonic epithelial cells. Moreover, we revealed that treatment with NADPH oxidase inhibitors had a protective effect against pro-inflammatory action of LPS in human colonic epithelium cells during inflammation.
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spelling pubmed-38345332013-11-21 Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis Ramonaite, Rima Skieceviciene, Jurgita Kiudelis, Gediminas Jonaitis, Laimas Tamelis, Algimantas Cizas, Paulius Borutaite, Vilmante Kupcinskas, Limas BMC Gastroenterol Research Article BACKGROUND: The aim of this study is to evaluate the role of NADPH oxidase in primary intestinal epithelial cells during the active phase of UC. METHODS: The primary human colonic epithelial cells were isolated from 19 patients with mild to moderate inflammatory activity of UC and 14 controls using chelation method. The cells were cultivated under the effect of mediators. Viability of cells was assessed by fluorescent microscopy. Production of reactive oxygen species (ROS) by the cells was measured fluorimetrically using Amplex Red. Production of TNF-α cytokine by the colonic epithelial cells was analysed by ELISA. RESULTS: The results of our study showed that unstimulated cells of UC patients had a decreased viability, increased ROS production, but similar TNF-α level when compared to the controls. Stimulation with LPS increased hydrogen peroxide and TNF-α level in the UC group. Treatment of colonic epithelial cells with NADPH oxidase inhibitor increased cell viability decreased the levels of ROS and TNF-α in the LPS-treated cells isolated from UC patients. CONCLUSIONS: Our study showed that bacterial endotoxins induced NADPH oxidase activation in the colonic epithelial cells. Moreover, we revealed that treatment with NADPH oxidase inhibitors had a protective effect against pro-inflammatory action of LPS in human colonic epithelium cells during inflammation. BioMed Central 2013-11-14 /pmc/articles/PMC3834533/ /pubmed/24229374 http://dx.doi.org/10.1186/1471-230X-13-159 Text en Copyright © 2013 Ramonaite et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ramonaite, Rima
Skieceviciene, Jurgita
Kiudelis, Gediminas
Jonaitis, Laimas
Tamelis, Algimantas
Cizas, Paulius
Borutaite, Vilmante
Kupcinskas, Limas
Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title_full Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title_fullStr Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title_full_unstemmed Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title_short Influence of NADPH oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
title_sort influence of nadph oxidase on inflammatory response in primary intestinal epithelial cells in patients with ulcerative colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834533/
https://www.ncbi.nlm.nih.gov/pubmed/24229374
http://dx.doi.org/10.1186/1471-230X-13-159
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