与年龄相关性听力损失有关的连接蛋白 30 和 43 表达变化

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Jennifer Pineros , Xiaoxia Zhu , Bo Ding , Robert D. Frisina
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引用次数: 0

摘要

老年性听力损失(ARHL)又称老花眼,是老年人的头号交流障碍。在包括耳蜗在内的整个人体中,细胞间通信都离不开连接蛋白。附件蛋白基因突变与人类综合征和非综合征性耳聋有关;因此,我们假设,随着年龄的增长,附件蛋白基因和蛋白表达的变化与 ARHL 的病因有关。在此,我们研究了不同年龄段 CBA/CaJ 小鼠的连接蛋白基因和蛋白表达变化,并分析了表达水平变化与 ABR 和 DPOAE 等功能性听力指标之间的相关性。此外,我们还研究了 ARHL 的潜在治疗方案。结果显示,Cx30 和 Cx43 基因表达明显下调,听力损失程度与这两个基因的表达变化之间存在明显的相关性。此外,利用耳蜗细胞系进行的剂量依赖性治疗表明,醛固酮激素疗法能显著增加 Cx 的表达。用醛固酮对小鼠进行体内治疗也显示出对老化小鼠中连接蛋白表达的保护作用。基于这些与功能相关的研究结果,下一步的研究可以包括更多地研究与 ARHL 期间连接蛋白家族缝隙连接蛋白表达变化相关的机制;以及通过了解 Cx 家族和相关细胞间蛋白的哪些特定成员应作为治疗目标,扩大对临床相关治疗方案的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Connexins 30 and 43 expression changes in relation to age-related hearing loss

Age-related hearing loss (ARHL), also known as presbycusis, is the number one communication disorder for aging adults. Connexin proteins are essential for intercellular communication throughout the human body, including the cochlea. Mutations in connexin genes have been linked to human syndromic and nonsyndromic deafness; thus, we hypothesize that changes in connexin gene and protein expression with age are involved in the etiology of ARHL. Here, connexin gene and protein expression changes for CBA/CaJ mice at different ages were examined, and correlations were analyzed between the changes in expression levels and functional hearing measures, such as ABRs and DPOAEs. Moreover, we investigated potential treatment options for ARHL. Results showed significant downregulation of Cx30 and Cx43 gene expression and significant correlations between the degree of hearing loss and the changes in gene expression for both genes. Moreover, dose-dependent treatments utilizing cochlear cell lines showed that aldosterone hormone therapy significantly increased Cx expression. In vivo mouse treatments with aldosterone also showed protective effects on connexin expression in aging mice. Based on these functionally relevant findings, next steps can include more investigations of the mechanisms related to connexin family gap junction protein expression changes during ARHL; and expand knowledge of clinically-relevant treatment options by knowing what specific members of the Cx family and related inter-cellular proteins should be targeted therapeutically.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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