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High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A

High Mobility Group Box1 (HMGB1), a damage-associated inflammatory factor, plays an important role in the pathogenesis of numerous chronic inflammatory and autoimmune diseases. In this study, the role of the HMGB1 in TcdA-induced ER stress was identified. Clostridium difficile toxin A is one of the...

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Detalles Bibliográficos
Autores principales: Liu, Ji, Ma, Yi, Sun, Chun-Li, Li, Shan, Wang, Ju-Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992521/
https://www.ncbi.nlm.nih.gov/pubmed/27579314
http://dx.doi.org/10.1155/2016/4130834
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author Liu, Ji
Ma, Yi
Sun, Chun-Li
Li, Shan
Wang, Ju-Fang
author_facet Liu, Ji
Ma, Yi
Sun, Chun-Li
Li, Shan
Wang, Ju-Fang
author_sort Liu, Ji
collection PubMed
description High Mobility Group Box1 (HMGB1), a damage-associated inflammatory factor, plays an important role in the pathogenesis of numerous chronic inflammatory and autoimmune diseases. In this study, the role of the HMGB1 in TcdA-induced ER stress was identified. Clostridium difficile toxin A is one of the major virulence factors of C. difficile infection (CDI) and has been proved to induce apoptotic cell death through ER stress. Our results showed that HMGB1 might play an important role in the TcdA-induced ER stress and unfolded protein response. HMGB1 activated molecular markers and induced the C/EBP homologous protein upregulation (CHOP). This study may provide the essential information for better understanding of the molecular mechanisms involved in CDI.
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spelling pubmed-49925212016-08-30 High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A Liu, Ji Ma, Yi Sun, Chun-Li Li, Shan Wang, Ju-Fang Biomed Res Int Research Article High Mobility Group Box1 (HMGB1), a damage-associated inflammatory factor, plays an important role in the pathogenesis of numerous chronic inflammatory and autoimmune diseases. In this study, the role of the HMGB1 in TcdA-induced ER stress was identified. Clostridium difficile toxin A is one of the major virulence factors of C. difficile infection (CDI) and has been proved to induce apoptotic cell death through ER stress. Our results showed that HMGB1 might play an important role in the TcdA-induced ER stress and unfolded protein response. HMGB1 activated molecular markers and induced the C/EBP homologous protein upregulation (CHOP). This study may provide the essential information for better understanding of the molecular mechanisms involved in CDI. Hindawi Publishing Corporation 2016 2016-08-07 /pmc/articles/PMC4992521/ /pubmed/27579314 http://dx.doi.org/10.1155/2016/4130834 Text en Copyright © 2016 Ji Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Ji
Ma, Yi
Sun, Chun-Li
Li, Shan
Wang, Ju-Fang
High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title_full High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title_fullStr High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title_full_unstemmed High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title_short High Mobility Group Box1 Protein Is Involved in Endoplasmic Reticulum Stress Induced by Clostridium difficile Toxin A
title_sort high mobility group box1 protein is involved in endoplasmic reticulum stress induced by clostridium difficile toxin a
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992521/
https://www.ncbi.nlm.nih.gov/pubmed/27579314
http://dx.doi.org/10.1155/2016/4130834
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