噪声性听力损失
赫拉
听力损失
生物
PI3K/AKT/mTOR通路
毛细胞
细胞生物学
耳蜗
噪声暴露
神经科学
医学
听力学
信号转导
遗传学
基因
突变
克拉斯
作者
Peng Chen,Chenhao Che,Lingjie Wu,Changjie Sun,Dongming Xu,Qinyang Hua,Yunzhong Zhang,Yi‐Quan Tang,Peng Shi,Shan Sun
标识
DOI:10.1002/advs.202508466
摘要
Abstract Noise‐induced hearing loss (NIHL), caused by irreversible cochlear hair cell (HC) damage, lacks effective therapies due to a limited understanding of endogenous protective mechanisms. The echolocating bats exhibit natural resistance to intense noise, and this suggested novel insights into methods to protect against NIHL. Here, through comparative transcriptomic analysis of noise‐exposed cochleae from the eastern bent‐winged bats ( Miniopterus fuliginosus ) and mice, the specific transcriptional dynamics in noise‐resistant Miniopterus fuliginosus are revealed, thus highlighting potential mechanisms for preventing cochlear damage that mouse models cannot replicate, with Hras emerging as the most significant hub upregulator. Functional validation in mice demonstrates that HC‐specific Hras overexpression significantly attenuates noise‐induced HC death, synaptic loss, and auditory threshold shifts. Mechanistically, Hras confers protection by activating the PI3K/Akt signaling pathway, a critical pro‐survival cascade. The findings further disentangle the mechanisms of cochlear resistance to intense noise in echolocating bats and suggest that targeting Hras expression may be a potential therapeutic intervention against NIHL.
科研通智能强力驱动
Strongly Powered by AbleSci AI