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TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction
Acquired cholesteatoma is a chronic inflammatory disease characterized by both hyperkeratinized squamous epithelial overgrowth and bone destruction. Toll-like receptor (TLR) activation and subsequent inflammatory cytokine production are closely associated with inflammatory bone disease. However, the...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671024/ https://www.ncbi.nlm.nih.gov/pubmed/26639190 http://dx.doi.org/10.1038/srep16683 |
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author | Si, Yu Chen, Yu Bin Chen, Sui Jun Zheng, Yi Qing Liu, Xiang Liu, Yi Jiang, Huai Li Xu, Guo Li, Zhuo Hao Huang, Qiu Hong Xiong, Hao Zhang, Zhi Gang |
author_facet | Si, Yu Chen, Yu Bin Chen, Sui Jun Zheng, Yi Qing Liu, Xiang Liu, Yi Jiang, Huai Li Xu, Guo Li, Zhuo Hao Huang, Qiu Hong Xiong, Hao Zhang, Zhi Gang |
author_sort | Si, Yu |
collection | PubMed |
description | Acquired cholesteatoma is a chronic inflammatory disease characterized by both hyperkeratinized squamous epithelial overgrowth and bone destruction. Toll-like receptor (TLR) activation and subsequent inflammatory cytokine production are closely associated with inflammatory bone disease. However, the expression and function of TLRs in cholesteatoma remain unclear.We observed inflammatory cell infiltration of the matrix and prematrix of human acquired cholesteatoma, as well as dramatically increased expression of TLR4 and the pro-inflammatory cytokines TNF-α and IL-1β. TLR2 exhibited an up-regulation that was not statistically significant. TLR4 expression in human acquired cholesteatoma correlated with disease severity; the number of TLR4-positive cells increased with an increased degree of cholesteatoma, invasion, bone destruction, and hearing loss. Moreover, TLR4 deficiency was protective against experimental acquired cholesteatoma-driven bone destruction and hearing loss, as it reduced local TNF-α and IL-1β expression and impaired osteoclast formation by decreasing expression of the osteoclast effectors receptor activator of nuclear factor (NF)-κB ligand (RANKL) and tartrate-resistant acid phosphatase (TRAP). TLR2 deficiency did not relieve disease severity, inflammatory responses, or osteoclast formation. Moreover, neither TLR2 nor TLR4 deficiency had an effect on antimicrobial peptides, inducible iNOS,BD-2 expression or bacterial clearance. Therefore, TLR4 may promote cholesteatoma-induced bone destruction and deafness by enhancing inflammatory responses and osteoclastogenesis. |
format | Online Article Text |
id | pubmed-4671024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46710242015-12-11 TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction Si, Yu Chen, Yu Bin Chen, Sui Jun Zheng, Yi Qing Liu, Xiang Liu, Yi Jiang, Huai Li Xu, Guo Li, Zhuo Hao Huang, Qiu Hong Xiong, Hao Zhang, Zhi Gang Sci Rep Article Acquired cholesteatoma is a chronic inflammatory disease characterized by both hyperkeratinized squamous epithelial overgrowth and bone destruction. Toll-like receptor (TLR) activation and subsequent inflammatory cytokine production are closely associated with inflammatory bone disease. However, the expression and function of TLRs in cholesteatoma remain unclear.We observed inflammatory cell infiltration of the matrix and prematrix of human acquired cholesteatoma, as well as dramatically increased expression of TLR4 and the pro-inflammatory cytokines TNF-α and IL-1β. TLR2 exhibited an up-regulation that was not statistically significant. TLR4 expression in human acquired cholesteatoma correlated with disease severity; the number of TLR4-positive cells increased with an increased degree of cholesteatoma, invasion, bone destruction, and hearing loss. Moreover, TLR4 deficiency was protective against experimental acquired cholesteatoma-driven bone destruction and hearing loss, as it reduced local TNF-α and IL-1β expression and impaired osteoclast formation by decreasing expression of the osteoclast effectors receptor activator of nuclear factor (NF)-κB ligand (RANKL) and tartrate-resistant acid phosphatase (TRAP). TLR2 deficiency did not relieve disease severity, inflammatory responses, or osteoclast formation. Moreover, neither TLR2 nor TLR4 deficiency had an effect on antimicrobial peptides, inducible iNOS,BD-2 expression or bacterial clearance. Therefore, TLR4 may promote cholesteatoma-induced bone destruction and deafness by enhancing inflammatory responses and osteoclastogenesis. Nature Publishing Group 2015-12-07 /pmc/articles/PMC4671024/ /pubmed/26639190 http://dx.doi.org/10.1038/srep16683 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Si, Yu Chen, Yu Bin Chen, Sui Jun Zheng, Yi Qing Liu, Xiang Liu, Yi Jiang, Huai Li Xu, Guo Li, Zhuo Hao Huang, Qiu Hong Xiong, Hao Zhang, Zhi Gang TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title | TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title_full | TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title_fullStr | TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title_full_unstemmed | TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title_short | TLR4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
title_sort | tlr4 drives the pathogenesis of acquired cholesteatoma by promoting local inflammation and bone destruction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4671024/ https://www.ncbi.nlm.nih.gov/pubmed/26639190 http://dx.doi.org/10.1038/srep16683 |
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