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miR-145b/AP2B1轴在雄性小鼠模型中导致噪声性感音神经性听力损失

miR-145b/AP2B1 Axis Contributes to Noise-induced Sensorineural Hearing Loss In a Male Mouse Model.

作者信息

Gu Xiang, Jiang Mengxian, Chen Wei

机构信息

Department of Otolaryngology, Head and Neck Surgery, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430000, China.

出版信息

Cell Biochem Biophys. 2025 Jun;83(2):2567-2575. doi: 10.1007/s12013-024-01665-3. Epub 2025 Jan 15.

Abstract

Sensorineural hearing loss (SNHL) is an increasingly prevalent sensory disorder, but the underlying mechanisms remain poorly understood. Adaptor related protein complex 2 subunit beta 1 (AP2B1) has been indicated to be detectable in mature cochleae. Nonetheless, it is unclear whether AP2B1 is implicated in the progression of SNHL. Male CBA/J mice were exposed to 2-20 kHz broadband noise at 96 or 101 dB SPL to induce temporary or permanent threshold shifts (TTS or PTS). Auditory brainstem responses were measured for hearing loss evaluation. Bioinformatics analysis was used to predict the upstream miRNAs of Ap2b1. RT-qPCR and western blotting were utilized to determine miR-145b and AP2B1 expression in mouse cochleae. Luciferase reporter assay was implemented to verify the interaction between Ap2b1 and miR-145b. Bioinformatics analysis identified miR-145b as an upstream miRNA of Ap2b1. AP2B1 expression was decreased and miR-145b expression was increased in mouse cochleae after PTS noise exposure. miR-145b targeted and negatively regulated Ap2b1 in PTS noise-exposed mice. Depletion of miR-145b alleviated auditory threshold shifts and outer hair cell loss in mice with exposure to PTS noise. In conclusion, inhibition of miR-145b ameliorates noise-induced SNHL in mice by upregulating AP2B1 expression.

摘要

感音神经性听力损失(SNHL)是一种日益普遍的感觉障碍,但其潜在机制仍知之甚少。已表明在成熟的耳蜗中可检测到衔接蛋白相关蛋白复合物2亚基β1(AP2B1)。然而,尚不清楚AP2B1是否与SNHL的进展有关。将雄性CBA/J小鼠暴露于96或101 dB SPL的2-20 kHz宽带噪声中,以诱导暂时性或永久性阈值偏移(TTS或PTS)。测量听觉脑干反应以评估听力损失。使用生物信息学分析来预测Ap2b1的上游miRNA。利用RT-qPCR和蛋白质印迹法测定小鼠耳蜗中miR-145b和AP2B1的表达。进行荧光素酶报告基因测定以验证Ap2b1与miR-145b之间的相互作用。生物信息学分析确定miR-145b为Ap2b1的上游miRNA。PTS噪声暴露后,小鼠耳蜗中AP2B1表达降低,miR-145b表达增加。在PTS噪声暴露的小鼠中,miR-145b靶向并负调控Ap2b1。miR-145b的缺失减轻了暴露于PTS噪声的小鼠的听觉阈值偏移和外毛细胞损失。总之,抑制miR-145b通过上调AP2B1表达改善小鼠噪声诱导的SNHL。

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