Role of Kir4.1 Channels in Aminoglycoside-Induced Ototoxicity of Hair Cells

被引:1
作者
Choi, Jin Sil [1 ,2 ]
Ahn, Ye Ji [1 ,2 ]
Lee, Suhoon [1 ,2 ]
Park, Dong Jun [1 ,2 ]
Park, Jeongeun [1 ,2 ]
Ha, Sun Mok [1 ,2 ]
Seo, Young Joon [1 ,2 ]
机构
[1] Yonsei Univ, Wonju Coll Med, Res Inst Hearing Enhancement, Wonju, South Korea
[2] Yonsei Univ, Wonju Coll Med, Dept Otorhinolaryngol, Wonju, South Korea
基金
新加坡国家研究基金会;
关键词
D O I
10.1155/2023/4191999
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The Kir4.1 channel, an inwardly rectifying potassium ion (K+) channel, is located in the hair cells of the organ of Corti as well as the intermediate cells of the stria vascularis. The Kir4.1 channel has a crucial role in the generation of endolymphatic potential and maintenance of the resting membrane potential. However, the role and functions of the Kir4.1 channel in the progenitor remain undescribed. To observe the role of Kir4.1 in the progenitor treated with the one-shot ototoxic drugs (kanamycin and furosemide), we set the proper condition in culturing Immortomouse-derived HEI-OC1 cells to express the potassium-related channels well. And also, that was reproduced in mice experiments to show the important role of Kir4.1 in the survival of hair cells after treating the ototoxicity drugs. In our results, when kanamycin and furosemide drugs were cotreated with HEI-OC1 cells, the Kir4.1 channel did not change, but the expression levels of the NKCC1 cotransporter and KCNQ4 channel are decreased. This shows that inward and outward channels were blocked by the two drugs (kanamycin and furosemide). However, noteworthy here is that the expression level of Kir4.1 channel increased when kanamycin was treated alone. This shows that Kir4.1, an inwardly rectifying potassium channel, acts as an outward channel in place of the corresponding channel when the KCNQ4 channel, an outward channel, is blocked. These results suggest that the Kir4.1 channel has a role in maintaining K+ homeostasis in supporting cells, with K+ concentration compensator when the NKCC1 cotransporter and Kv7.4 (KCNQ4) channels are deficient.
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页数:12
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