AAV-mediated NT-3 overexpression protects cochleae against noise-induced synaptopathy

被引:54
作者
Chen, Hengchao [1 ]
Xing, Yazhi [1 ]
Xia, Li [1 ]
Chen, Zhengnong [1 ]
Yin, Shankai [1 ]
Wang, Jian [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Otolaryngol Res Inst, Affiliated Hosp 6, Shanghai, Peoples R China
[2] Dalhousie Univ, Sch Human Commun Disorders, Halifax, NS, Canada
关键词
HIDDEN HEARING-LOSS; SPIRAL GANGLION NEURONS; NEUROTROPHIC FACTORS; CODING DEFICITS; RIBBON SYNAPSES; AUDITORY-NERVE; NEUROPATHY; RESPONSES; EXPOSURE; NUCLEUS;
D O I
10.1038/s41434-018-0012-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synapse between inner hair cells (IHCs) and type I spiral ganglion neurons (SGNs) has been identified as a sensitive structure to noise-induced damage in the mammalian cochlea. Since this synapse provides the major information pathway from the cochlea to the auditory brain, it is important to maintain its integrity. Neurotrophin-3 (NT-3) has been known to play an important role in the development and the functional maintenance of this synapse. Application of exogenous NT-3, or overexpression of this gene in a transgenic animal model, have shown the value to protect this synapse from noise-induced damage. In the present study, NT-3 overexpression was induced by cochlear gene transfection before noise exposure via the use of an adeno-associated viral (AAV) vector. We found that such an overexpression provided a significant synaptic protection against a noise exposure that caused massive damage to the synapses, likely due to it promoting the repair of the synapse after the initial damage.
引用
收藏
页码:251 / 259
页数:9
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