Transient Receptor Potential Cation Channel Subfamily Vanilloid 4 and 3 in the Inner Ear Protect Hearing in Mice

被引:5
|
作者
Wang, Shengnan [1 ,2 ,3 ,4 ]
Geng, Qiaowei [1 ,2 ,3 ,4 ]
Huo, Lifang [2 ,3 ,5 ]
Ma, Yirui [1 ,2 ,3 ,4 ]
Gao, Yiting [1 ,2 ,3 ,4 ]
Zhang, Wei [2 ,3 ,5 ]
Zhang, Hailin [1 ,2 ,3 ,4 ]
Lv, Ping [1 ,2 ,3 ,4 ]
Jia, Zhanfeng [1 ,2 ,3 ,4 ]
机构
[1] Hebei Med Univ, Dept Pharmacol, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Ctr Innovat Drug Res & Evaluat, Inst Med Sci & Hlth, Shijiazhuang, Hebei, Peoples R China
[3] Minist Educ, Key Lab Neural & Vasc Biol, Shijiazhuang, Hebei, Peoples R China
[4] Key Lab New Drug Pharmacol & Toxicol, Shijiazhuang, Hebei, Peoples R China
[5] Hebei Med Univ, Inst Chinese Integrat Med, Dept Pharmacol, Shijiazhuang, Hebei, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
cochlear hair cell; TRPV; TRPV3; knockout; hearing; OUTER HAIR-CELLS; MECHANOTRANSDUCTION MACHINERY; TRPV3; CHANNEL; EXPRESSION; CONTRIBUTES; MUTATION; HEAT; IMPAIRMENT; KANAMYCIN; COMPONENT;
D O I
10.3389/fnmol.2019.00296
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The transient receptor potential cation channel, vanilloid type (TRPV) 3, is a member of the TRPV subfamily that is expressed predominantly in the skin, hair follicles, and gastrointestinal tract. It is also distributed in the organ of Corti of the inner ear and colocalizes with TRPV1 or TRPV4, but its role in auditory function is unknown. In the present study, we demonstrate that TRPV3 is expressed in inner hair cells (HCs) but mainly in cochlear outer HCs in mice, with expression limited to the cytoplasm and not detected in stereocilia. We compared the number of HCs as well as distortion product otoacoustic emissions (DPOAE) and auditory brainstem response (ABR) thresholds between TRPV3 knockout (V3KO) and wild-type (V3WT) mice and found that although most mutants (72.3%) had normal hearing, a significant proportion (27.7%) showed impaired hearing associated with loss of cochlear HCs. Compensatory upregulation of TRPV4 in HCs prevented HC damage and kanamycin-induced hearing loss and preserved normal auditory function in most of these mice. Thus, TRPV4 and TRPV3 in cochlear HCs protect hearing in mice; moreover, the results suggest some functional redundancy in the functions of TRPV family members. Our findings provide novel insight into the molecular basis of auditory function in mammals that can be applied to the development of strategies to mitigate hearing loss.
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页数:13
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