Cargando…

Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation

BACKGROUND/AIMS: Bacteria-derived outer membrane vesicles (OMVs) are commonly associated with various biological activities and functions. Helicobacter pylori-derived OMVs are thought to contribute to pathogenesis. This study aimed to investigate the effects of H. pylori-derived OMVs. METHODS: H. py...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Mun Sun, Ze, Eun Young, Park, Jae Yong, Shin, Tae-Seop, Kim, Jae Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273812/
https://www.ncbi.nlm.nih.gov/pubmed/33242939
http://dx.doi.org/10.3904/kjim.2019.432
_version_ 1783721444570562560
author Choi, Mun Sun
Ze, Eun Young
Park, Jae Yong
Shin, Tae-Seop
Kim, Jae Gyu
author_facet Choi, Mun Sun
Ze, Eun Young
Park, Jae Yong
Shin, Tae-Seop
Kim, Jae Gyu
author_sort Choi, Mun Sun
collection PubMed
description BACKGROUND/AIMS: Bacteria-derived outer membrane vesicles (OMVs) are commonly associated with various biological activities and functions. Helicobacter pylori-derived OMVs are thought to contribute to pathogenesis. This study aimed to investigate the effects of H. pylori-derived OMVs. METHODS: H. pylori strains were isolated from patients with gastritis, gastric ulcer, or gastric cancer using endoscopic biopsy. The U-937, AGS, and MKN-45 cell lines were exposed to H. pylori and H. pylori-derived OMVs. The expression of interleukin 8 (IL-8) messenger RNA (mRNA) was assessed using reverse transcription-polymerase chain reaction (RT-PCR) and real-time RT-PCR, and IL-8 secretion was analyzed using enzyme-linked immunosorbent assay. Nuclear factor kappa B (NF-κB) activation was evaluated by Western blotting. RESULTS: H. pylori and H. pylori-derived OMVs induced the expression of IL-8 mRNA and protein. Importantly, the bacteria induced higher IL-8 mRNA and protein expression than the OMVs. IL-8 expression was induced to different levels in response to H. pylori-derived OMVs from hosts with different gastric diseases. Western blotting revealed the increased phosphorylation and reduced degradation of inhibitor of NF-κB alpha in cells exposed to OMVs. CONCLUSIONS: H. pylori-derived OMVs may aid the development of various gastric diseases by inducing IL-8 production and NF-κB activation.
format Online
Article
Text
id pubmed-8273812
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Korean Association of Internal Medicine
record_format MEDLINE/PubMed
spelling pubmed-82738122021-07-20 Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation Choi, Mun Sun Ze, Eun Young Park, Jae Yong Shin, Tae-Seop Kim, Jae Gyu Korean J Intern Med Original Article BACKGROUND/AIMS: Bacteria-derived outer membrane vesicles (OMVs) are commonly associated with various biological activities and functions. Helicobacter pylori-derived OMVs are thought to contribute to pathogenesis. This study aimed to investigate the effects of H. pylori-derived OMVs. METHODS: H. pylori strains were isolated from patients with gastritis, gastric ulcer, or gastric cancer using endoscopic biopsy. The U-937, AGS, and MKN-45 cell lines were exposed to H. pylori and H. pylori-derived OMVs. The expression of interleukin 8 (IL-8) messenger RNA (mRNA) was assessed using reverse transcription-polymerase chain reaction (RT-PCR) and real-time RT-PCR, and IL-8 secretion was analyzed using enzyme-linked immunosorbent assay. Nuclear factor kappa B (NF-κB) activation was evaluated by Western blotting. RESULTS: H. pylori and H. pylori-derived OMVs induced the expression of IL-8 mRNA and protein. Importantly, the bacteria induced higher IL-8 mRNA and protein expression than the OMVs. IL-8 expression was induced to different levels in response to H. pylori-derived OMVs from hosts with different gastric diseases. Western blotting revealed the increased phosphorylation and reduced degradation of inhibitor of NF-κB alpha in cells exposed to OMVs. CONCLUSIONS: H. pylori-derived OMVs may aid the development of various gastric diseases by inducing IL-8 production and NF-κB activation. Korean Association of Internal Medicine 2021-07 2020-12-01 /pmc/articles/PMC8273812/ /pubmed/33242939 http://dx.doi.org/10.3904/kjim.2019.432 Text en Copyright © 2021 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Mun Sun
Ze, Eun Young
Park, Jae Yong
Shin, Tae-Seop
Kim, Jae Gyu
Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title_full Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title_fullStr Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title_full_unstemmed Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title_short Helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa B activation
title_sort helicobacter pylori-derived outer membrane vesicles stimulate interleukin 8 secretion through nuclear factor kappa b activation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273812/
https://www.ncbi.nlm.nih.gov/pubmed/33242939
http://dx.doi.org/10.3904/kjim.2019.432
work_keys_str_mv AT choimunsun helicobacterpyloriderivedoutermembranevesiclesstimulateinterleukin8secretionthroughnuclearfactorkappabactivation
AT zeeunyoung helicobacterpyloriderivedoutermembranevesiclesstimulateinterleukin8secretionthroughnuclearfactorkappabactivation
AT parkjaeyong helicobacterpyloriderivedoutermembranevesiclesstimulateinterleukin8secretionthroughnuclearfactorkappabactivation
AT shintaeseop helicobacterpyloriderivedoutermembranevesiclesstimulateinterleukin8secretionthroughnuclearfactorkappabactivation
AT kimjaegyu helicobacterpyloriderivedoutermembranevesiclesstimulateinterleukin8secretionthroughnuclearfactorkappabactivation