Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.

A recent study revealed that Slitrk6, a transmembrane protein containing a leucine-rich repeat domain, has a critical role in the development of the inner ear neural circuit. However, it is still unknown how the absence of Slitrk6 affects auditory and vestibular functions. In addition, the role of S...

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Autores principales: Yoshifumi Matsumoto, Kei-ichi Katayama, Takehito Okamoto, Kazuyuki Yamada, Noriko Takashima, Soichi Nagao, Jun Aruga
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:e128d9fecd934c4f843fabbc2cb03f2d2021-11-18T06:59:51ZImpaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.1932-620310.1371/journal.pone.0016497https://doaj.org/article/e128d9fecd934c4f843fabbc2cb03f2d2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21298075/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203A recent study revealed that Slitrk6, a transmembrane protein containing a leucine-rich repeat domain, has a critical role in the development of the inner ear neural circuit. However, it is still unknown how the absence of Slitrk6 affects auditory and vestibular functions. In addition, the role of Slitrk6 in regions of the central nervous system, including the dorsal thalamus, has not been addressed. To understand the physiological role of Slitrk6, Slitrk6-knockout (KO) mice were subjected to systematic behavioral analyses including auditory and vestibular function tests. Compared to wild-type mice, the auditory brainstem response (ABR) of Slitrk6-KO mice indicated a mid-frequency range (8-16 kHz) hearing loss and reduction of the first ABR wave. The auditory startle response was also reduced. A vestibulo-ocular reflex (VOR) test showed decreased vertical (head movement-induced) VOR gains and normal horizontal VOR. In an open field test, locomotor activity was reduced; the tendency to be in the center region was increased, but only in the first 5 min of the test, indicating altered adaptive responses to a novel environment. Altered adaptive responses were also found in a hole-board test in which head-dip behavior was increased and advanced. Aside from these abnormalities, no clear abnormalities were noted in the mood, anxiety, learning, spatial memory, or fear memory-related behavioral tests. These results indicate that the Slitrk6-KO mouse can serve as a model of hereditary sensorineural deafness. Furthermore, the altered responses of Slitrk6-KO mice to the novel environment suggest a role of Slitrk6 in some cognitive functions.Yoshifumi MatsumotoKei-ichi KatayamaTakehito OkamotoKazuyuki YamadaNoriko TakashimaSoichi NagaoJun ArugaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 1, p e16497 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Yoshifumi Matsumoto
Kei-ichi Katayama
Takehito Okamoto
Kazuyuki Yamada
Noriko Takashima
Soichi Nagao
Jun Aruga
Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
description A recent study revealed that Slitrk6, a transmembrane protein containing a leucine-rich repeat domain, has a critical role in the development of the inner ear neural circuit. However, it is still unknown how the absence of Slitrk6 affects auditory and vestibular functions. In addition, the role of Slitrk6 in regions of the central nervous system, including the dorsal thalamus, has not been addressed. To understand the physiological role of Slitrk6, Slitrk6-knockout (KO) mice were subjected to systematic behavioral analyses including auditory and vestibular function tests. Compared to wild-type mice, the auditory brainstem response (ABR) of Slitrk6-KO mice indicated a mid-frequency range (8-16 kHz) hearing loss and reduction of the first ABR wave. The auditory startle response was also reduced. A vestibulo-ocular reflex (VOR) test showed decreased vertical (head movement-induced) VOR gains and normal horizontal VOR. In an open field test, locomotor activity was reduced; the tendency to be in the center region was increased, but only in the first 5 min of the test, indicating altered adaptive responses to a novel environment. Altered adaptive responses were also found in a hole-board test in which head-dip behavior was increased and advanced. Aside from these abnormalities, no clear abnormalities were noted in the mood, anxiety, learning, spatial memory, or fear memory-related behavioral tests. These results indicate that the Slitrk6-KO mouse can serve as a model of hereditary sensorineural deafness. Furthermore, the altered responses of Slitrk6-KO mice to the novel environment suggest a role of Slitrk6 in some cognitive functions.
format article
author Yoshifumi Matsumoto
Kei-ichi Katayama
Takehito Okamoto
Kazuyuki Yamada
Noriko Takashima
Soichi Nagao
Jun Aruga
author_facet Yoshifumi Matsumoto
Kei-ichi Katayama
Takehito Okamoto
Kazuyuki Yamada
Noriko Takashima
Soichi Nagao
Jun Aruga
author_sort Yoshifumi Matsumoto
title Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
title_short Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
title_full Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
title_fullStr Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
title_full_unstemmed Impaired auditory-vestibular functions and behavioral abnormalities of Slitrk6-deficient mice.
title_sort impaired auditory-vestibular functions and behavioral abnormalities of slitrk6-deficient mice.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/e128d9fecd934c4f843fabbc2cb03f2d
work_keys_str_mv AT yoshifumimatsumoto impairedauditoryvestibularfunctionsandbehavioralabnormalitiesofslitrk6deficientmice
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