Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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
_version_ 1782404346704560128
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
work_keys_str_mv AT siyu tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT chenyubin tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT chensuijun tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT zhengyiqing tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT liuxiang tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT liuyi tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT jianghuaili tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT xuguo tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT lizhuohao tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT huangqiuhong tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT xionghao tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction
AT zhangzhigang tlr4drivesthepathogenesisofacquiredcholesteatomabypromotinglocalinflammationandbonedestruction