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Oxidative stress-mediated HMGB1 biology

High mobility group box 1 (HMGB1) is a widely-expressed and highly-abundant protein that acts as an extracellular signal upon active secretion by immune cells or passive release by dead, dying, and injured cells. Both intracellular and extracellular HMGB1 play pivotal roles in regulation of the cell...

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Detalles Bibliográficos
Autores principales: Yu, Yan, Tang, Daolin, Kang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387954/
https://www.ncbi.nlm.nih.gov/pubmed/25904867
http://dx.doi.org/10.3389/fphys.2015.00093
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author Yu, Yan
Tang, Daolin
Kang, Rui
author_facet Yu, Yan
Tang, Daolin
Kang, Rui
author_sort Yu, Yan
collection PubMed
description High mobility group box 1 (HMGB1) is a widely-expressed and highly-abundant protein that acts as an extracellular signal upon active secretion by immune cells or passive release by dead, dying, and injured cells. Both intracellular and extracellular HMGB1 play pivotal roles in regulation of the cellular response to stress. Targeting the translocation, release, and activity of HMGB1 can limit inflammation and reduce tissue damage during infection and sterile inflammation. Although the mechanisms contributing to HMGB1 biology are still under investigation, it appears that oxidative stress is a central regulator of HMGB1's translocation, release, and activity in inflammation and cell death (e.g., necrosis, apoptosis, autophagic cell death, pyroptosis, and NETosis). Thus, targeting HMGB1 with antioxidant compounds may be an attractive therapeutic strategy for inflammation-associated diseases such as sepsis, ischemia and reperfusion injury, arthritis, diabetes, and cancer.
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spelling pubmed-43879542015-04-22 Oxidative stress-mediated HMGB1 biology Yu, Yan Tang, Daolin Kang, Rui Front Physiol Physiology High mobility group box 1 (HMGB1) is a widely-expressed and highly-abundant protein that acts as an extracellular signal upon active secretion by immune cells or passive release by dead, dying, and injured cells. Both intracellular and extracellular HMGB1 play pivotal roles in regulation of the cellular response to stress. Targeting the translocation, release, and activity of HMGB1 can limit inflammation and reduce tissue damage during infection and sterile inflammation. Although the mechanisms contributing to HMGB1 biology are still under investigation, it appears that oxidative stress is a central regulator of HMGB1's translocation, release, and activity in inflammation and cell death (e.g., necrosis, apoptosis, autophagic cell death, pyroptosis, and NETosis). Thus, targeting HMGB1 with antioxidant compounds may be an attractive therapeutic strategy for inflammation-associated diseases such as sepsis, ischemia and reperfusion injury, arthritis, diabetes, and cancer. Frontiers Media S.A. 2015-04-07 /pmc/articles/PMC4387954/ /pubmed/25904867 http://dx.doi.org/10.3389/fphys.2015.00093 Text en Copyright © 2015 Yu, Tang and Kang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Yu, Yan
Tang, Daolin
Kang, Rui
Oxidative stress-mediated HMGB1 biology
title Oxidative stress-mediated HMGB1 biology
title_full Oxidative stress-mediated HMGB1 biology
title_fullStr Oxidative stress-mediated HMGB1 biology
title_full_unstemmed Oxidative stress-mediated HMGB1 biology
title_short Oxidative stress-mediated HMGB1 biology
title_sort oxidative stress-mediated hmgb1 biology
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387954/
https://www.ncbi.nlm.nih.gov/pubmed/25904867
http://dx.doi.org/10.3389/fphys.2015.00093
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