Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models

被引:3
作者
Wang, Li [1 ,2 ]
Guan, Jing [1 ]
Wang, Hongyang [1 ]
Lan, Lan [1 ]
Zhang, Qiujing [1 ]
Zong, Liang [1 ]
Du, Wan [1 ]
Xiong, Wenping [1 ]
Li, Fengjiao [1 ]
Wu, Kaiwen [1 ]
Wang, Dayong [1 ]
Wang, Qiuju [1 ]
机构
[1] Med Sch Chinese PLA, Chinese PLA Gen Hosp, Inst Otolaryngol, Beijing 100853, Peoples R China
[2] Nankai Univ, Coll Med, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
auditory neuropathy spectrum disorder; transgenic mouse models; pathogenesis; systematic review; HEARING IMPAIRMENT; MICE; MUTATIONS; SYNAPSE; RISK; PHENOTYPE; STRAINS; LESION; NERVE; CELLS;
D O I
10.1007/s11427-015-4985-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Auditory neuropathy spectrum disorder is a unique group of hearing dysfunctions characterized by preserved outer hair cell function and abnormal neural conduction of the auditory pathway. However, the pathogenic mechanism underlying this disorder is not clear. We therefore performed a systematic review of genetic mouse models with different gene mutations to provide a valuable tool for better understanding of the process and the possible molecular mechanisms. Of the 18 articles retrieved, nine met the required criteria. All biochemical, histological, and electrophysiological results were recorded for each of the mouse models, as was the transgenic technology. This review provides a summary of different mouse models that may play an important role in the diagnosis and management of auditory neuropathy spectrum disorder in the future.
引用
收藏
页码:480 / 486
页数:7
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