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Downregulated UCHL1 Accelerates Gentamicin-Induced Auditory Cell Death via Autophagy

DC Field Value Language
dc.contributor.authorKim, YJ-
dc.contributor.authorKim, K-
dc.contributor.authorLee, YY-
dc.contributor.authorChoo, OS-
dc.contributor.authorJang, JH-
dc.contributor.authorChoung, YH-
dc.date.accessioned2020-10-21T07:21:34Z-
dc.date.available2020-10-21T07:21:34Z-
dc.date.issued2019-
dc.identifier.issn0893-7648-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/18942-
dc.description.abstractThe clinical use of aminoglycoside antibiotics is partly limited by their ototoxicity. The pathogenesis of aminoglycoside-induced ototoxicity still remains unknown. Here, RNA-sequencing was conducted to identify differentially expressed genes in rat cochlear organotypic cultures treated with gentamicin (GM), and 232 and 43 genes were commonly up- and downregulated, respectively, at day 1 and 2 after exposure. Ubiquitin carboxyl-terminal hydrolase isozyme L1 (Uchl1) was one of the downregulated genes whose expression was prominent in spiral ganglion cells (SGCs), lateral walls, as well as efferent nerve terminal and nerve fibers. We further investigated if a deficit of Uchl1 in organotypic cochlea and the House Ear Institute-Organ of Corti 1 (HEI-OC1) cells accelerates ototoxicity. We found that a deficit in Uchl1 accelerated GM-induced ototoxicity by showing a decreased number of SGCs and nerve fibers in organotypic cochlear cultures and HEI-OC1 cells. Furthermore, Uchl1-depleted HEI-OC1 cells revealed an increased number of autophagosomes accompanied by decreased lysosomal fusion. These data indicate that the downregulation of Uchl1 following GM treatment is deleterious to auditory cell survival, which results from the impaired autophagic flux. Our results provide evidence that UCHL1-dependent autophagic flux may have a potential as an otoprotective target for the treatment of GM-induced auditory cell death.-
dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAutophagosomes-
dc.subject.MESHAutophagy-
dc.subject.MESHCell Line-
dc.subject.MESHDown-Regulation-
dc.subject.MESHGene Expression Profiling-
dc.subject.MESHGentamicins-
dc.subject.MESHHair Cells, Auditory-
dc.subject.MESHHumans-
dc.subject.MESHProtein Interaction Mapping-
dc.subject.MESHRats, Sprague-Dawley-
dc.subject.MESHSequestosome-1 Protein-
dc.subject.MESHUbiquitin Thiolesterase-
dc.subject.MESHUp-Regulation-
dc.subject.MESHbeta Catenin-
dc.titleDownregulated UCHL1 Accelerates Gentamicin-Induced Auditory Cell Death via Autophagy-
dc.typeArticle-
dc.identifier.pmid31041655-
dc.subject.keywordAminoglycoside-
dc.subject.keywordAutophagic flux-
dc.subject.keywordOtotoxicity-
dc.subject.keywordRNA-sequencing-
dc.subject.keywordUCHL1-
dc.contributor.affiliatedAuthor김, 연주-
dc.contributor.affiliatedAuthor이, 윤영-
dc.contributor.affiliatedAuthor추, 옥성-
dc.contributor.affiliatedAuthor장, 정훈-
dc.contributor.affiliatedAuthor정, 연훈-
dc.type.localJournal Papers-
dc.identifier.doi10.1007/s12035-019-1598-y-
dc.citation.titleMolecular neurobiology-
dc.citation.volume56-
dc.citation.number11-
dc.citation.date2019-
dc.citation.startPage7433-
dc.citation.endPage7447-
dc.identifier.bibliographicCitationMolecular neurobiology, 56(11). : 7433-7447, 2019-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn1559-1182-
dc.relation.journalidJ008937648-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Otolaryngology
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