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听力障碍中的微小RNA:氧化应激、炎症和抗氧化剂对它们的调控

MicroRNAs in Hearing Disorders: Their Regulation by Oxidative Stress, Inflammation and Antioxidants.

作者信息

Prasad Kedar N, Bondy Stephen C

机构信息

Engage GlobalSan Rafael, CA, United States.

Center for Occupational and Environmental Health, Department of Medicine, University of California, IrvineIrvine, CA, United States.

出版信息

Front Cell Neurosci. 2017 Sep 11;11:276. doi: 10.3389/fncel.2017.00276. eCollection 2017.

Abstract

MicroRNAs (miRs) are small non-coding single-stranded RNAs that bind to their complimentary sequences in the 3'-untranslated regions (3'-UTRs) of the target mRNAs that prevent their translation into the corresponding proteins. Since miRs are strongly expressed in cells of inner ear and play a role in regulating their differentiation, survival and function, alterations in their expression may be involved in the pathogenesis of hearing disorders. Although increased oxidative stress and inflammation are involved in initiation and progression of hearing disorders, it is unknown whether the mechanisms of damage produced by these biochemical events on inner ear cells are mediated by altering the expression of miRs. In neurons and non-neuronal cells, reactive oxygen species (ROS) and pro-inflammatory cytokines mediate their damaging effects by altering the expression of miRs. Preliminary data indicate that a similar mechanism of damage on hair cells produced by oxidative stress may exist in this disease. Antioxidants protect against hearing disorders induced by ototoxic agents or adverse health conditions; however, it is unknown whether the protective effects of antioxidants in hearing disorders are mediated by changing the expression of miRs. Antioxidants protect mammalian cells against oxidative damage by changing the expression of miRs. Therefore, it is proposed that a similar mechanism of protection by antioxidants against stress may be found in hearing disorders. This review article discusses novel concepts: (a) alterations in the expression of miRs may be involved in the pathogenesis of hearing disorders; (b) presents evidence from neurons and glia cells to show that oxidative stress and pro-inflammatory cytokines mediate their damaging effects by altering the expression of miRs; and proposes that a similar mechanism of damage by these biochemical events may be found in hearing loss; and (c) present data to show that antioxidants protect mammalian cells against oxidative by altering the expression of miRs. A similar role of antioxidants in protecting against hearing disorders is put forward. New studies are proposed to fill the gaps in the areas listed above.

摘要

微小RNA(miRs)是小的非编码单链RNA,它们与靶mRNA的3'非翻译区(3'-UTR)中的互补序列结合,从而阻止其翻译成相应的蛋白质。由于miRs在内耳细胞中强烈表达并在调节其分化、存活和功能中发挥作用,其表达改变可能与听力障碍的发病机制有关。虽然氧化应激增加和炎症参与听力障碍的发生和发展,但尚不清楚这些生化事件对内耳细胞产生损伤的机制是否是通过改变miRs的表达介导的。在神经元和非神经元细胞中,活性氧(ROS)和促炎细胞因子通过改变miRs的表达介导其损伤作用。初步数据表明,这种疾病中可能存在由氧化应激对毛细胞产生损伤的类似机制。抗氧化剂可预防由耳毒性药物或不良健康状况引起的听力障碍;然而,尚不清楚抗氧化剂在听力障碍中的保护作用是否是通过改变miRs的表达介导的。抗氧化剂通过改变miRs的表达保护哺乳动物细胞免受氧化损伤。因此,有人提出在听力障碍中可能发现抗氧化剂对抗应激的类似保护机制。这篇综述文章讨论了新的概念:(a)miRs表达的改变可能参与听力障碍的发病机制;(b)提供来自神经元和神经胶质细胞的证据,表明氧化应激和促炎细胞因子通过改变miRs的表达介导其损伤作用,并提出在听力损失中可能发现这些生化事件的类似损伤机制;(c)展示数据表明抗氧化剂通过改变miRs的表达保护哺乳动物细胞免受氧化损伤。提出了抗氧化剂在预防听力障碍中类似的作用。建议进行新的研究以填补上述领域的空白。

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