Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways
Noise-induced hearing loss (NIHL) is characterized by damage to cochlear neurons and associated hair cells; however, a systematic evaluation of NIHL pathogenesis is still lacking. Here, we systematically evaluated differentially expressed genes of 22 cochlear samples in an NIHL mouse model. We perfo...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-08-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2020.00968/full |
id |
doaj-4a45d4248a334fe9bd5aaac6e3949895 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Quan Wang Quan Wang Yilin Shen Yilin Shen Haixia Hu Haixia Hu Cui Fan Cui Fan Andi Zhang Andi Zhang Rui Ding Rui Ding Bin Ye Bin Ye Mingliang Xiang Mingliang Xiang |
spellingShingle |
Quan Wang Quan Wang Yilin Shen Yilin Shen Haixia Hu Haixia Hu Cui Fan Cui Fan Andi Zhang Andi Zhang Rui Ding Rui Ding Bin Ye Bin Ye Mingliang Xiang Mingliang Xiang Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways Frontiers in Genetics systematically evaluation diagnostic value NIHL pathogenesis spiral ganglion neurons functional annotation |
author_facet |
Quan Wang Quan Wang Yilin Shen Yilin Shen Haixia Hu Haixia Hu Cui Fan Cui Fan Andi Zhang Andi Zhang Rui Ding Rui Ding Bin Ye Bin Ye Mingliang Xiang Mingliang Xiang |
author_sort |
Quan Wang |
title |
Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways |
title_short |
Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways |
title_full |
Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways |
title_fullStr |
Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways |
title_full_unstemmed |
Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and Pathways |
title_sort |
systematic transcriptome analysis of noise-induced hearing loss pathogenesis suggests inflammatory activities and multiple susceptible molecules and pathways |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Genetics |
issn |
1664-8021 |
publishDate |
2020-08-01 |
description |
Noise-induced hearing loss (NIHL) is characterized by damage to cochlear neurons and associated hair cells; however, a systematic evaluation of NIHL pathogenesis is still lacking. Here, we systematically evaluated differentially expressed genes of 22 cochlear samples in an NIHL mouse model. We performed Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis and weighted gene co-expression network analysis (WGCNA). Core modules were detected using protein–protein interactions and WGCNA with functional annotation, diagnostic value evaluation, and experimental validation. Pooled functional annotation suggested the involvement of multiple inflammatory pathways, including the TNF signaling pathway, IL-17 signaling pathway, NF-kappa B signaling pathway, rheumatoid arthritis, and p53 signaling pathway. The core modules suggested that responses to cytokines, heat, cAMP, ATP, mechanical stimuli, and immune responses were important in NIHL pathogenesis. These activities primarily occurred on the external side of the plasma membrane, the extracellular region, and the nucleus. Binding activities, including CCR2 receptor binding, protein binding, and transcription factor binding, may be important. Additionally, the hub molecules with diagnostic value included Relb, Hspa1b, Ccl2, Ptgs2, Ldlr, Plat, and Ccl17. An evaluation of Relb and Hspa1b protein levels showed that Relb was upregulated in spiral ganglion neurons, which might have diagnostic value. In conclusion, this study indicates that the inflammatory response is involved in auditory organ changes in NIHL pathogenesis; moreover, several molecules and activities have essential and subtle influences that have translational potential for pharmacological intervention. |
topic |
systematically evaluation diagnostic value NIHL pathogenesis spiral ganglion neurons functional annotation |
url |
https://www.frontiersin.org/article/10.3389/fgene.2020.00968/full |
work_keys_str_mv |
AT quanwang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT quanwang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT yilinshen systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT yilinshen systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT haixiahu systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT haixiahu systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT cuifan systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT cuifan systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT andizhang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT andizhang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT ruiding systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT ruiding systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT binye systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT binye systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT mingliangxiang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways AT mingliangxiang systematictranscriptomeanalysisofnoiseinducedhearinglosspathogenesissuggestsinflammatoryactivitiesandmultiplesusceptiblemoleculesandpathways |
_version_ |
1724459915621171200 |
spelling |
doaj-4a45d4248a334fe9bd5aaac6e39498952020-11-25T03:57:35ZengFrontiers Media S.A.Frontiers in Genetics1664-80212020-08-011110.3389/fgene.2020.00968563593Systematic Transcriptome Analysis of Noise-Induced Hearing Loss Pathogenesis Suggests Inflammatory Activities and Multiple Susceptible Molecules and PathwaysQuan Wang0Quan Wang1Yilin Shen2Yilin Shen3Haixia Hu4Haixia Hu5Cui Fan6Cui Fan7Andi Zhang8Andi Zhang9Rui Ding10Rui Ding11Bin Ye12Bin Ye13Mingliang Xiang14Mingliang Xiang15Department of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaDepartment of Otolaryngology & Head and Neck Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaEar Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, ChinaNoise-induced hearing loss (NIHL) is characterized by damage to cochlear neurons and associated hair cells; however, a systematic evaluation of NIHL pathogenesis is still lacking. Here, we systematically evaluated differentially expressed genes of 22 cochlear samples in an NIHL mouse model. We performed Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis and weighted gene co-expression network analysis (WGCNA). Core modules were detected using protein–protein interactions and WGCNA with functional annotation, diagnostic value evaluation, and experimental validation. Pooled functional annotation suggested the involvement of multiple inflammatory pathways, including the TNF signaling pathway, IL-17 signaling pathway, NF-kappa B signaling pathway, rheumatoid arthritis, and p53 signaling pathway. The core modules suggested that responses to cytokines, heat, cAMP, ATP, mechanical stimuli, and immune responses were important in NIHL pathogenesis. These activities primarily occurred on the external side of the plasma membrane, the extracellular region, and the nucleus. Binding activities, including CCR2 receptor binding, protein binding, and transcription factor binding, may be important. Additionally, the hub molecules with diagnostic value included Relb, Hspa1b, Ccl2, Ptgs2, Ldlr, Plat, and Ccl17. An evaluation of Relb and Hspa1b protein levels showed that Relb was upregulated in spiral ganglion neurons, which might have diagnostic value. In conclusion, this study indicates that the inflammatory response is involved in auditory organ changes in NIHL pathogenesis; moreover, several molecules and activities have essential and subtle influences that have translational potential for pharmacological intervention.https://www.frontiersin.org/article/10.3389/fgene.2020.00968/fullsystematically evaluationdiagnostic valueNIHL pathogenesisspiral ganglion neuronsfunctional annotation |