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High-mobility group box protein 1 expression in inflammatory diseases of the middle ear

High-mobility group box 1 (HMGB1) is a nuclear non-histone protein, playing a critical role as a mediator between innate and acquired immunity; when released extracellularly, it coordinates the cellular stress response (under necrosis, bacterial lipopolysaccharide stimulation) and acts as an inflamm...

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Autores principales: Bellussi, Luisa Maria, Vindigni, Carla, Cocca, Serena, Butorano, Marie Aimee Gloria Munezero, Livi, Walter, Corallo, Giulia, Passali, Desiderio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806793/
https://www.ncbi.nlm.nih.gov/pubmed/28555513
http://dx.doi.org/10.1177/0394632017698713
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author Bellussi, Luisa Maria
Vindigni, Carla
Cocca, Serena
Butorano, Marie Aimee Gloria Munezero
Livi, Walter
Corallo, Giulia
Passali, Desiderio
author_facet Bellussi, Luisa Maria
Vindigni, Carla
Cocca, Serena
Butorano, Marie Aimee Gloria Munezero
Livi, Walter
Corallo, Giulia
Passali, Desiderio
author_sort Bellussi, Luisa Maria
collection PubMed
description High-mobility group box 1 (HMGB1) is a nuclear non-histone protein, playing a critical role as a mediator between innate and acquired immunity; when released extracellularly, it coordinates the cellular stress response (under necrosis, bacterial lipopolysaccharide stimulation) and acts as an inflammatory marker and cytokine. The aim of the study was to demonstrate whether HMGB1 is over-expressed in chronic middle-ear pathologies and whether the entity of expression and the localization are correlated with the degree of the inflammatory reaction, thus suggesting that HMGB1 may play a crucial role in chronic inflammatory disorders of the middle ear, as already demonstrated in other airway diseases. We analyzed 30 samples of middle-ear mucosa in patients affected by chronic suppurative otitis media with ear drum perforation with/without cholesteatoma and otosclerosis as control. The distribution of HMGB1 was evaluated as nuclear, cytoplasmic, and/or extracellular staining. The inflammatory cells observed in the biopsies were mostly lymphocytes and plasmacells. A statistically significant difference in inflammation score between otosclerosis and chronic otitis samples (P < 0.01; Anova test) and between otosclerosis and cholesteatoma samples (P < 0.05; Anova test) was observed; the HMGB1 positivity was in accordance with the density of the inflammatory infiltrate. HMGB1 is over-expressed in chronic middle-ear pathologies and may play a role in the progression of the inflammatory process from recurrent acute otitis media to chronic suppurative otitis media.
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spelling pubmed-58067932018-02-28 High-mobility group box protein 1 expression in inflammatory diseases of the middle ear Bellussi, Luisa Maria Vindigni, Carla Cocca, Serena Butorano, Marie Aimee Gloria Munezero Livi, Walter Corallo, Giulia Passali, Desiderio Int J Immunopathol Pharmacol Letters to the Editor High-mobility group box 1 (HMGB1) is a nuclear non-histone protein, playing a critical role as a mediator between innate and acquired immunity; when released extracellularly, it coordinates the cellular stress response (under necrosis, bacterial lipopolysaccharide stimulation) and acts as an inflammatory marker and cytokine. The aim of the study was to demonstrate whether HMGB1 is over-expressed in chronic middle-ear pathologies and whether the entity of expression and the localization are correlated with the degree of the inflammatory reaction, thus suggesting that HMGB1 may play a crucial role in chronic inflammatory disorders of the middle ear, as already demonstrated in other airway diseases. We analyzed 30 samples of middle-ear mucosa in patients affected by chronic suppurative otitis media with ear drum perforation with/without cholesteatoma and otosclerosis as control. The distribution of HMGB1 was evaluated as nuclear, cytoplasmic, and/or extracellular staining. The inflammatory cells observed in the biopsies were mostly lymphocytes and plasmacells. A statistically significant difference in inflammation score between otosclerosis and chronic otitis samples (P < 0.01; Anova test) and between otosclerosis and cholesteatoma samples (P < 0.05; Anova test) was observed; the HMGB1 positivity was in accordance with the density of the inflammatory infiltrate. HMGB1 is over-expressed in chronic middle-ear pathologies and may play a role in the progression of the inflammatory process from recurrent acute otitis media to chronic suppurative otitis media. SAGE Publications 2017-03-15 2017-06 /pmc/articles/PMC5806793/ /pubmed/28555513 http://dx.doi.org/10.1177/0394632017698713 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Letters to the Editor
Bellussi, Luisa Maria
Vindigni, Carla
Cocca, Serena
Butorano, Marie Aimee Gloria Munezero
Livi, Walter
Corallo, Giulia
Passali, Desiderio
High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title_full High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title_fullStr High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title_full_unstemmed High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title_short High-mobility group box protein 1 expression in inflammatory diseases of the middle ear
title_sort high-mobility group box protein 1 expression in inflammatory diseases of the middle ear
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806793/
https://www.ncbi.nlm.nih.gov/pubmed/28555513
http://dx.doi.org/10.1177/0394632017698713
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