C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.

Hearing depends on the transduction of sounds into neural signals by the inner hair cells of the cochlea. Cochleae also have outer hair cells with unique electromotile properties that increase auditory sensitivity, but they are particularly susceptible to damage by intense noise exposure, ototoxic d...

Full description

Bibliographic Details
Main Authors: Joyshree Biswas, Robert S Pijewski, Rohit Makol, Tania G Miramontes, Brianna L Thompson, Lyndsay C Kresic, Alice L Burghard, Douglas L Oliver, David C Martinelli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0251412
_version_ 1819100963974152192
author Joyshree Biswas
Robert S Pijewski
Rohit Makol
Tania G Miramontes
Brianna L Thompson
Lyndsay C Kresic
Alice L Burghard
Douglas L Oliver
David C Martinelli
author_facet Joyshree Biswas
Robert S Pijewski
Rohit Makol
Tania G Miramontes
Brianna L Thompson
Lyndsay C Kresic
Alice L Burghard
Douglas L Oliver
David C Martinelli
author_sort Joyshree Biswas
collection DOAJ
description Hearing depends on the transduction of sounds into neural signals by the inner hair cells of the cochlea. Cochleae also have outer hair cells with unique electromotile properties that increase auditory sensitivity, but they are particularly susceptible to damage by intense noise exposure, ototoxic drugs, and aging. Although the outer hair cells have synapses on afferent neurons that project to the brain, the function of this neuronal circuit is unclear. Here, we created a novel mouse allele that inserts a fluorescent reporter at the C1ql1 locus which revealed gene expression in the outer hair cells and allowed creation of outer hair cell-specific C1ql1 knockout mice. We found that C1ql1 expression in outer hair cells corresponds to areas with the most sensitive frequencies of the mouse audiogram, and that it has an unexpected adolescence-onset developmental timing. No expression was observed in the inner hair cells. Since C1QL1 in the brain is made by neurons, transported anterogradely in axons, and functions in the synaptic cleft, C1QL1 may serve a similar function at the outer hair cell afferent synapse. Histological analyses revealed that C1ql1 conditional knockout cochleae may have reduced outer hair cell afferent synapse maintenance. However, auditory behavioral and physiological assays did not reveal a compelling phenotype. Nonetheless, this study identifies a potentially useful gene expressed in the cochlea and opens the door for future studies aimed at elucidating the function of C1QL1 and the function of the outer hair cell and its afferent neurons.
first_indexed 2024-12-22T01:11:08Z
format Article
id doaj.art-b615781f72aa4e369175c54ab0732d98
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-22T01:11:08Z
publishDate 2021-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-b615781f72aa4e369175c54ab0732d982022-12-21T18:43:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01165e025141210.1371/journal.pone.0251412C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.Joyshree BiswasRobert S PijewskiRohit MakolTania G MiramontesBrianna L ThompsonLyndsay C KresicAlice L BurghardDouglas L OliverDavid C MartinelliHearing depends on the transduction of sounds into neural signals by the inner hair cells of the cochlea. Cochleae also have outer hair cells with unique electromotile properties that increase auditory sensitivity, but they are particularly susceptible to damage by intense noise exposure, ototoxic drugs, and aging. Although the outer hair cells have synapses on afferent neurons that project to the brain, the function of this neuronal circuit is unclear. Here, we created a novel mouse allele that inserts a fluorescent reporter at the C1ql1 locus which revealed gene expression in the outer hair cells and allowed creation of outer hair cell-specific C1ql1 knockout mice. We found that C1ql1 expression in outer hair cells corresponds to areas with the most sensitive frequencies of the mouse audiogram, and that it has an unexpected adolescence-onset developmental timing. No expression was observed in the inner hair cells. Since C1QL1 in the brain is made by neurons, transported anterogradely in axons, and functions in the synaptic cleft, C1QL1 may serve a similar function at the outer hair cell afferent synapse. Histological analyses revealed that C1ql1 conditional knockout cochleae may have reduced outer hair cell afferent synapse maintenance. However, auditory behavioral and physiological assays did not reveal a compelling phenotype. Nonetheless, this study identifies a potentially useful gene expressed in the cochlea and opens the door for future studies aimed at elucidating the function of C1QL1 and the function of the outer hair cell and its afferent neurons.https://doi.org/10.1371/journal.pone.0251412
spellingShingle Joyshree Biswas
Robert S Pijewski
Rohit Makol
Tania G Miramontes
Brianna L Thompson
Lyndsay C Kresic
Alice L Burghard
Douglas L Oliver
David C Martinelli
C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
PLoS ONE
title C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
title_full C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
title_fullStr C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
title_full_unstemmed C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
title_short C1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient.
title_sort c1ql1 is expressed in adult outer hair cells of the cochlea in a tonotopic gradient
url https://doi.org/10.1371/journal.pone.0251412
work_keys_str_mv AT joyshreebiswas c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT robertspijewski c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT rohitmakol c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT taniagmiramontes c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT briannalthompson c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT lyndsayckresic c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT alicelburghard c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT douglasloliver c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient
AT davidcmartinelli c1ql1isexpressedinadultouterhaircellsofthecochleainatonotopicgradient