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Reappraisal of oxidized HMGB1 as a mediator and biomarker

HMGB1 is a dual-function protein that acts as a chromatin-binding protein and as a danger-associated molecular pattern (DAMP) when released from activated immune cells or injured tissue. In much of the HMGB1 literature, immunomodulatory effects of extracellular HMGB1 are proposed to depend on its ox...

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Autores principales: Pirnie, Ross, P Gillespie, Kevin, Mesaros, Clementina, Blair, Ian A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979160/
https://www.ncbi.nlm.nih.gov/pubmed/36874369
http://dx.doi.org/10.2144/fsoa-2022-0052
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author Pirnie, Ross
P Gillespie, Kevin
Mesaros, Clementina
Blair, Ian A
author_facet Pirnie, Ross
P Gillespie, Kevin
Mesaros, Clementina
Blair, Ian A
author_sort Pirnie, Ross
collection PubMed
description HMGB1 is a dual-function protein that acts as a chromatin-binding protein and as a danger-associated molecular pattern (DAMP) when released from activated immune cells or injured tissue. In much of the HMGB1 literature, immunomodulatory effects of extracellular HMGB1 are proposed to depend on its oxidation state. However, many of the foundational studies for this model have been retracted or flagged with expressions of concern. The literature on HMGB1 oxidation reveals a diversity of redox proteoforms of HMGB1 that are inconsistent with current models of redox modulation regulating HMGB1 secretion. A recent study of acetaminophen toxicity has identified previously unrecognized HMGB1 oxidized proteoforms. HMGB1 undergoes oxidative modifications that could serve as pathology-specific biomarkers and drug targets.
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spelling pubmed-99791602023-03-03 Reappraisal of oxidized HMGB1 as a mediator and biomarker Pirnie, Ross P Gillespie, Kevin Mesaros, Clementina Blair, Ian A Future Sci OA Review HMGB1 is a dual-function protein that acts as a chromatin-binding protein and as a danger-associated molecular pattern (DAMP) when released from activated immune cells or injured tissue. In much of the HMGB1 literature, immunomodulatory effects of extracellular HMGB1 are proposed to depend on its oxidation state. However, many of the foundational studies for this model have been retracted or flagged with expressions of concern. The literature on HMGB1 oxidation reveals a diversity of redox proteoforms of HMGB1 that are inconsistent with current models of redox modulation regulating HMGB1 secretion. A recent study of acetaminophen toxicity has identified previously unrecognized HMGB1 oxidized proteoforms. HMGB1 undergoes oxidative modifications that could serve as pathology-specific biomarkers and drug targets. Future Science Ltd 2023-02-10 /pmc/articles/PMC9979160/ /pubmed/36874369 http://dx.doi.org/10.2144/fsoa-2022-0052 Text en © 2023 Ian A. Blair https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Pirnie, Ross
P Gillespie, Kevin
Mesaros, Clementina
Blair, Ian A
Reappraisal of oxidized HMGB1 as a mediator and biomarker
title Reappraisal of oxidized HMGB1 as a mediator and biomarker
title_full Reappraisal of oxidized HMGB1 as a mediator and biomarker
title_fullStr Reappraisal of oxidized HMGB1 as a mediator and biomarker
title_full_unstemmed Reappraisal of oxidized HMGB1 as a mediator and biomarker
title_short Reappraisal of oxidized HMGB1 as a mediator and biomarker
title_sort reappraisal of oxidized hmgb1 as a mediator and biomarker
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979160/
https://www.ncbi.nlm.nih.gov/pubmed/36874369
http://dx.doi.org/10.2144/fsoa-2022-0052
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