Cargando…

MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss

Congenital cytomegalovirus (CMV) infection is the most common infectious cause of sensorineural hearing loss in children. While the importance of CMV-induced SNHL has been described, the mechanisms underlying its pathogenesis and the role of inflammatory responses remain elusive. The present study e...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhuang, Wei, Wang, Caiji, Shi, Xi, Qiu, Shiwei, Zhang, Shili, Xu, Bing, Chen, Min, Jiang, Wen, Dong, Hongyan, Qiao, Yuehua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881649/
https://www.ncbi.nlm.nih.gov/pubmed/29512778
http://dx.doi.org/10.3892/ijmm.2018.3539
_version_ 1783311354077118464
author Zhuang, Wei
Wang, Caiji
Shi, Xi
Qiu, Shiwei
Zhang, Shili
Xu, Bing
Chen, Min
Jiang, Wen
Dong, Hongyan
Qiao, Yuehua
author_facet Zhuang, Wei
Wang, Caiji
Shi, Xi
Qiu, Shiwei
Zhang, Shili
Xu, Bing
Chen, Min
Jiang, Wen
Dong, Hongyan
Qiao, Yuehua
author_sort Zhuang, Wei
collection PubMed
description Congenital cytomegalovirus (CMV) infection is the most common infectious cause of sensorineural hearing loss in children. While the importance of CMV-induced SNHL has been described, the mechanisms underlying its pathogenesis and the role of inflammatory responses remain elusive. The present study established an experimental model of hearing loss after systemic infection with murine CMV (MCMV) in newborn mice. Auditory brainstem responses were tested to evaluate hearing at 3 weeks, expression of inflammasome-associated factors was assessed by immunofluorescence, western blot analysis, reverse transcription-quantitative polymerase chain reaction and ELISA. MCMV sequentially induced inflammasome-associated factors. Furthermore, the inflammasome-associated factors were also increased in cultured spiral ganglion neurons infected with MCMV for 24 h. In addition, MCMV increased the content of reactive oxygen species (ROS). These results suggest that hearing loss caused by MCMV infection may be associated with ROS-induced inflammation.
format Online
Article
Text
id pubmed-5881649
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-58816492018-04-12 MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss Zhuang, Wei Wang, Caiji Shi, Xi Qiu, Shiwei Zhang, Shili Xu, Bing Chen, Min Jiang, Wen Dong, Hongyan Qiao, Yuehua Int J Mol Med Articles Congenital cytomegalovirus (CMV) infection is the most common infectious cause of sensorineural hearing loss in children. While the importance of CMV-induced SNHL has been described, the mechanisms underlying its pathogenesis and the role of inflammatory responses remain elusive. The present study established an experimental model of hearing loss after systemic infection with murine CMV (MCMV) in newborn mice. Auditory brainstem responses were tested to evaluate hearing at 3 weeks, expression of inflammasome-associated factors was assessed by immunofluorescence, western blot analysis, reverse transcription-quantitative polymerase chain reaction and ELISA. MCMV sequentially induced inflammasome-associated factors. Furthermore, the inflammasome-associated factors were also increased in cultured spiral ganglion neurons infected with MCMV for 24 h. In addition, MCMV increased the content of reactive oxygen species (ROS). These results suggest that hearing loss caused by MCMV infection may be associated with ROS-induced inflammation. D.A. Spandidos 2018-06 2018-03-06 /pmc/articles/PMC5881649/ /pubmed/29512778 http://dx.doi.org/10.3892/ijmm.2018.3539 Text en Copyright: © Zhuang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhuang, Wei
Wang, Caiji
Shi, Xi
Qiu, Shiwei
Zhang, Shili
Xu, Bing
Chen, Min
Jiang, Wen
Dong, Hongyan
Qiao, Yuehua
MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title_full MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title_fullStr MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title_full_unstemmed MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title_short MCMV triggers ROS/NLRP3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
title_sort mcmv triggers ros/nlrp3-associated inflammasome activation in the inner ear of mice and cultured spiral ganglion neurons, contributing to sensorineural hearing loss
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881649/
https://www.ncbi.nlm.nih.gov/pubmed/29512778
http://dx.doi.org/10.3892/ijmm.2018.3539
work_keys_str_mv AT zhuangwei mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT wangcaiji mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT shixi mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT qiushiwei mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT zhangshili mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT xubing mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT chenmin mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT jiangwen mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT donghongyan mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss
AT qiaoyuehua mcmvtriggersrosnlrp3associatedinflammasomeactivationintheinnerearofmiceandculturedspiralganglionneuronscontributingtosensorineuralhearingloss