GDF15 在通过减轻氧化应激减轻噪声引起的隐性听力损失方面的作用

IF 5.3 2区 医学 Q2 CELL BIOLOGY
Yihong Jiang, Zeyu Zheng, Jing Zhu, Peng Zhang, Shaoheng Li, Yang Fu, Fei Wang, Zhuoru Zhang, Tong Chang, Min Zhang, Bai Ruan, Xiaocheng Wang
{"title":"GDF15 在通过减轻氧化应激减轻噪声引起的隐性听力损失方面的作用","authors":"Yihong Jiang, Zeyu Zheng, Jing Zhu, Peng Zhang, Shaoheng Li, Yang Fu, Fei Wang, Zhuoru Zhang, Tong Chang, Min Zhang, Bai Ruan, Xiaocheng Wang","doi":"10.1007/s10565-024-09912-2","DOIUrl":null,"url":null,"abstract":"<p>Noise-induced hidden hearing loss (HHL) is a newly uncovered form of hearing impairment that causes hidden damage to the cochlea. Patients with HHL do not have significant abnormalities in their hearing thresholds, but they experience impaired speech recognition in noisy environments. However, the mechanisms underlying HHL remain unclear. In this study, we developed single-cell transcriptome profiles of the cochlea of mice with HHL, detailing changes in individual cell types. Our study revealed a transient threshold shift, reduced auditory brainstem response wave I amplitude, and decreased number of ribbon synapses in HHL mice. Our findings suggest elevated oxidative stress and GDF15 expression in cochlear hair cells of HHL mice. Notably, the upregulation of GDF15 attenuated oxidative stress and auditory impairment in the cochlea of HHL mice. This suggests that a therapeutic strategy targeting GDF15 may be efficacious against HHL.</p><h3 data-test=\"abstract-sub-heading\">Graphical Abstract</h3><ol>\n<li>\n<span>1.</span>\n<p>HHL mice had a transient threshold shift, reduced ABR wave I amplitude, and decreased number of ribbon synapses.</p>\n</li>\n<li>\n<span>2.</span>\n<p>HHL mice's cochlear hair cells exhibited increased oxidative stress and elevated GDF15 expression.</p>\n</li>\n<li>\n<span>3.</span>\n<p>Upregulation of GDF15 attenuated oxidative stress and auditory damage in the cochlea of HHL mice, implying that GDF15-targeted treatment techniques may be useful for HHL.</p>\n</li>\n</ol>\n","PeriodicalId":9672,"journal":{"name":"Cell Biology and Toxicology","volume":"24 1","pages":""},"PeriodicalIF":5.3000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The role of GDF15 in attenuating noise-induced hidden hearing loss by alleviating oxidative stress\",\"authors\":\"Yihong Jiang, Zeyu Zheng, Jing Zhu, Peng Zhang, Shaoheng Li, Yang Fu, Fei Wang, Zhuoru Zhang, Tong Chang, Min Zhang, Bai Ruan, Xiaocheng Wang\",\"doi\":\"10.1007/s10565-024-09912-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Noise-induced hidden hearing loss (HHL) is a newly uncovered form of hearing impairment that causes hidden damage to the cochlea. Patients with HHL do not have significant abnormalities in their hearing thresholds, but they experience impaired speech recognition in noisy environments. However, the mechanisms underlying HHL remain unclear. In this study, we developed single-cell transcriptome profiles of the cochlea of mice with HHL, detailing changes in individual cell types. Our study revealed a transient threshold shift, reduced auditory brainstem response wave I amplitude, and decreased number of ribbon synapses in HHL mice. Our findings suggest elevated oxidative stress and GDF15 expression in cochlear hair cells of HHL mice. Notably, the upregulation of GDF15 attenuated oxidative stress and auditory impairment in the cochlea of HHL mice. This suggests that a therapeutic strategy targeting GDF15 may be efficacious against HHL.</p><h3 data-test=\\\"abstract-sub-heading\\\">Graphical Abstract</h3><ol>\\n<li>\\n<span>1.</span>\\n<p>HHL mice had a transient threshold shift, reduced ABR wave I amplitude, and decreased number of ribbon synapses.</p>\\n</li>\\n<li>\\n<span>2.</span>\\n<p>HHL mice's cochlear hair cells exhibited increased oxidative stress and elevated GDF15 expression.</p>\\n</li>\\n<li>\\n<span>3.</span>\\n<p>Upregulation of GDF15 attenuated oxidative stress and auditory damage in the cochlea of HHL mice, implying that GDF15-targeted treatment techniques may be useful for HHL.</p>\\n</li>\\n</ol>\\n\",\"PeriodicalId\":9672,\"journal\":{\"name\":\"Cell Biology and Toxicology\",\"volume\":\"24 1\",\"pages\":\"\"},\"PeriodicalIF\":5.3000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell Biology and Toxicology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10565-024-09912-2\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Biology and Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10565-024-09912-2","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

噪声诱发的隐性听力损失(HHL)是一种新发现的听力损伤形式,会对耳蜗造成隐性损伤。HHL 患者的听阈没有明显异常,但他们在嘈杂环境中的言语识别能力会受到损害。然而,HHL 的发病机制仍不清楚。在这项研究中,我们绘制了 HHL 小鼠耳蜗的单细胞转录组图谱,详细描述了单个细胞类型的变化。我们的研究揭示了 HHL 小鼠的瞬时阈值偏移、听觉脑干反应波 I 振幅降低以及带状突触数量减少。我们的研究结果表明,HHL 小鼠耳蜗毛细胞的氧化应激和 GDF15 表达升高。值得注意的是,GDF15的上调减轻了HHL小鼠耳蜗中的氧化应激和听觉损伤。图解摘要1.HHL小鼠有瞬时阈值偏移、ABR波I振幅降低和带状突触数量减少。3.GDF15的上调减轻了HHL小鼠耳蜗中的氧化应激和听觉损伤,这意味着GDF15靶向治疗技术可能对HHL有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The role of GDF15 in attenuating noise-induced hidden hearing loss by alleviating oxidative stress

The role of GDF15 in attenuating noise-induced hidden hearing loss by alleviating oxidative stress

Noise-induced hidden hearing loss (HHL) is a newly uncovered form of hearing impairment that causes hidden damage to the cochlea. Patients with HHL do not have significant abnormalities in their hearing thresholds, but they experience impaired speech recognition in noisy environments. However, the mechanisms underlying HHL remain unclear. In this study, we developed single-cell transcriptome profiles of the cochlea of mice with HHL, detailing changes in individual cell types. Our study revealed a transient threshold shift, reduced auditory brainstem response wave I amplitude, and decreased number of ribbon synapses in HHL mice. Our findings suggest elevated oxidative stress and GDF15 expression in cochlear hair cells of HHL mice. Notably, the upregulation of GDF15 attenuated oxidative stress and auditory impairment in the cochlea of HHL mice. This suggests that a therapeutic strategy targeting GDF15 may be efficacious against HHL.

Graphical Abstract

  1. 1.

    HHL mice had a transient threshold shift, reduced ABR wave I amplitude, and decreased number of ribbon synapses.

  2. 2.

    HHL mice's cochlear hair cells exhibited increased oxidative stress and elevated GDF15 expression.

  3. 3.

    Upregulation of GDF15 attenuated oxidative stress and auditory damage in the cochlea of HHL mice, implying that GDF15-targeted treatment techniques may be useful for HHL.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Cell Biology and Toxicology
Cell Biology and Toxicology 生物-毒理学
CiteScore
9.90
自引率
4.90%
发文量
101
审稿时长
>12 weeks
期刊介绍: Cell Biology and Toxicology (CBT) is an international journal focused on clinical and translational research with an emphasis on molecular and cell biology, genetic and epigenetic heterogeneity, drug discovery and development, and molecular pharmacology and toxicology. CBT has a disease-specific scope prioritizing publications on gene and protein-based regulation, intracellular signaling pathway dysfunction, cell type-specific function, and systems in biomedicine in drug discovery and development. CBT publishes original articles with outstanding, innovative and significant findings, important reviews on recent research advances and issues of high current interest, opinion articles of leading edge science, and rapid communication or reports, on molecular mechanisms and therapies in diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信