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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2011
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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) |
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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 |
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