老年性聋
衰老
基因敲除
生物
细胞生物学
信号转导
基因
基因表达
神经科学
细胞
感觉系统
炎症
遗传学
机制(生物学)
小RNA
作者
Jingjing Wu,Xiaowen Liu,Daxue Zhu,Bo Xu,Yufen Guo
出处
期刊:Neuroscience
[Elsevier BV]
日期:2025-10-15
卷期号:588: 128-141
标识
DOI:10.1016/j.neuroscience.2025.10.018
摘要
Presbycusis, or age-related hearing loss (ARHL), is a prevalent sensory disorder in the elderly, driven by genetic factors, oxidative stress, inflammation responses, and cellular senescence. Despite its significance, the molecular mechanisms underlying ARHL remain poorly defined. In this study, we employed bioinformatic analysis of public gene expression datasets to identify differentially expressed genes in ARHL. Protein-protein interaction network analysis further nominated LCN2 as a hub gene. Experimental validation in aging C57BL/6J mice and HEI-OC1 auditory cells revealed that elevated LCN2 expression promotes cellular senescence, while its knockdown delays this phenotype. Mechanistically, LCN2 drives senescence by activating the NF-κB signaling pathway, and its inhibition alleviates senescence induced by tert-butyl hydroperoxide (TBHP). Our findings establish LCN2 as a key pro-senescence factor in ARHL and demonstrate that it regulates auditory cell senescence through the NF-κB pathway, providing new mechanistic insights and revealing potential therapeutic targets for ARHL intervention.
科研通智能强力驱动
Strongly Powered by AbleSci AI