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

Authors :
Choi JS
Ahn YJ
Lee S
Park DJ
Park J
Ha SM
Seo YJ
Source :
BioMed research international [Biomed Res Int] 2023 Dec 16; Vol. 2023, pp. 4191999. Date of Electronic Publication: 2023 Dec 16 (Print Publication: 2023).
Publication Year :
2023

Abstract

The Kir4.1 channel, an inwardly rectifying potassium ion (K <superscript>+</superscript> ) 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 <superscript>+</superscript> homeostasis in supporting cells, with K <superscript>+</superscript> concentration compensator when the NKCC1 cotransporter and Kv7.4 (KCNQ4) channels are deficient.<br />Competing Interests: The authors declare that there is no conflict of interest regarding the publication of this article.<br /> (Copyright © 2023 Jin Sil Choi et al.)

Details

Language :
English
ISSN :
2314-6141
Volume :
2023
Database :
MEDLINE
Journal :
BioMed research international
Publication Type :
Academic Journal
Accession number :
38143588
Full Text :
https://doi.org/10.1155/2023/4191999