The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.

Acoustic trauma, one of the leading causes of sensorineural hearing loss, induces sensory hair cell damage in the cochlea. Identifying the molecular mechanisms involved in regulating sensory hair cell death is critical towards developing effective treatments for preventing hair cell damage. Recently...

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Main Authors: Minal Patel, Qunfeng Cai, Dalian Ding, Richard Salvi, Zihua Hu, Bo Hua Hu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3589350?pdf=render
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spelling doaj-cab3598853054cab84e1694db4aca6ab2020-11-25T01:05:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5847110.1371/journal.pone.0058471The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.Minal PatelQunfeng CaiDalian DingRichard SalviZihua HuBo Hua HuAcoustic trauma, one of the leading causes of sensorineural hearing loss, induces sensory hair cell damage in the cochlea. Identifying the molecular mechanisms involved in regulating sensory hair cell death is critical towards developing effective treatments for preventing hair cell damage. Recently, microRNAs (miRNAs) have been shown to participate in the regulatory mechanisms of inner ear development and homeostasis. However, their involvement in cochlear sensory cell degeneration following acoustic trauma is unknown. Here, we profiled the expression pattern of miRNAs in the cochlear sensory epithelium, defined miRNA responses to acoustic overstimulation, and explored potential mRNA targets of miRNAs that may be responsible for the stress responses of the cochlea. Expression analysis of miRNAs in the cochlear sensory epithelium revealed constitutive expression of 176 miRNAs, many of which have not been previously reported in cochlear tissue. Exposure to intense noise caused significant threshold shift and apoptotic activity in the cochleae. Gene expression analysis of noise-traumatized cochleae revealed time-dependent transcriptional changes in the expression of miRNAs. Target prediction analysis revealed potential target genes of the significantly downregulated miRNAs, many of which had cell death- and apoptosis-related functions. Verification of the predicted targets revealed a significant upregulation of Taok1, a target of miRNA-183. Moreover, inhibition of miR-183 with morpholino antisense oligos in cochlear organotypic cultures revealed a negative correlation between the expression levels of miR-183 and Taok1, suggesting the presence of a miR-183/Taok1 target pair. Together, miRNA profiling as well as the target analysis and validation suggest the involvement of miRNAs in the regulation of the degenerative process of the cochlea following acoustic overstimulation. The miR-183/Taok1 target pair is likely to play a role in this regulatory process.http://europepmc.org/articles/PMC3589350?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Minal Patel
Qunfeng Cai
Dalian Ding
Richard Salvi
Zihua Hu
Bo Hua Hu
spellingShingle Minal Patel
Qunfeng Cai
Dalian Ding
Richard Salvi
Zihua Hu
Bo Hua Hu
The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
PLoS ONE
author_facet Minal Patel
Qunfeng Cai
Dalian Ding
Richard Salvi
Zihua Hu
Bo Hua Hu
author_sort Minal Patel
title The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
title_short The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
title_full The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
title_fullStr The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
title_full_unstemmed The miR-183/Taok1 target pair is implicated in cochlear responses to acoustic trauma.
title_sort mir-183/taok1 target pair is implicated in cochlear responses to acoustic trauma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Acoustic trauma, one of the leading causes of sensorineural hearing loss, induces sensory hair cell damage in the cochlea. Identifying the molecular mechanisms involved in regulating sensory hair cell death is critical towards developing effective treatments for preventing hair cell damage. Recently, microRNAs (miRNAs) have been shown to participate in the regulatory mechanisms of inner ear development and homeostasis. However, their involvement in cochlear sensory cell degeneration following acoustic trauma is unknown. Here, we profiled the expression pattern of miRNAs in the cochlear sensory epithelium, defined miRNA responses to acoustic overstimulation, and explored potential mRNA targets of miRNAs that may be responsible for the stress responses of the cochlea. Expression analysis of miRNAs in the cochlear sensory epithelium revealed constitutive expression of 176 miRNAs, many of which have not been previously reported in cochlear tissue. Exposure to intense noise caused significant threshold shift and apoptotic activity in the cochleae. Gene expression analysis of noise-traumatized cochleae revealed time-dependent transcriptional changes in the expression of miRNAs. Target prediction analysis revealed potential target genes of the significantly downregulated miRNAs, many of which had cell death- and apoptosis-related functions. Verification of the predicted targets revealed a significant upregulation of Taok1, a target of miRNA-183. Moreover, inhibition of miR-183 with morpholino antisense oligos in cochlear organotypic cultures revealed a negative correlation between the expression levels of miR-183 and Taok1, suggesting the presence of a miR-183/Taok1 target pair. Together, miRNA profiling as well as the target analysis and validation suggest the involvement of miRNAs in the regulation of the degenerative process of the cochlea following acoustic overstimulation. The miR-183/Taok1 target pair is likely to play a role in this regulatory process.
url http://europepmc.org/articles/PMC3589350?pdf=render
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