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  1. 050 医学部, 大学院医学系研究科
  2. 0501 学術論文

Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells

http://hdl.handle.net/10091/00021596
http://hdl.handle.net/10091/00021596
783ad1ee-a291-4af3-998c-04f3a3771fad
名前 / ファイル ライセンス アクション
26293369_05.pdf 26293369_05.pdf (1.2 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2019-09-09
タイトル
タイトル Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells
言語
言語 eng
DOI
関連識別子 https://doi.org/10.1242/bio.20147799
関連名称 10.1242/bio.20147799
キーワード
主題 Occludin, Deafness, Tight junction, Cochlea, Hair cell, Tricellulin
資源タイプ
資源 http://purl.org/coar/resource_type/c_6501
タイプ journal article
著者 Kitajiri, Shin-ichiro

× Kitajiri, Shin-ichiro

en Kitajiri, Shin-ichiro

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Katsuno, Tatsuya

× Katsuno, Tatsuya

en Katsuno, Tatsuya

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Sasaki, Hiroyuki

× Sasaki, Hiroyuki

en Sasaki, Hiroyuki

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Ito, Juichi

× Ito, Juichi

en Ito, Juichi

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Furuse, Mikio

× Furuse, Mikio

en Furuse, Mikio

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Tsukita, Shoichiro

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en Tsukita, Shoichiro

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信州大学研究者総覧へのリンク
氏名 Kitajiri, Shin-ichiro
URL http://soar-rd.shinshu-u.ac.jp/profile/ja.jUTCupyC.html
出版者
出版者 COMPANY OF BIOLOGISTS LTD
引用
内容記述 BIOLOGY OPEN.3(8):759-766(2014)
書誌情報 BIOLOGY OPEN

巻 3, 号 8, p. 759-766, 発行日 2014-08-15
抄録
内容記述 Occludin is the first identified protein in the tight junction (TJ), but its function has remained for the most part obscure. TJs have been demonstrated to play important roles in the inner ear function, and occludin is expressed in all the epithelial TJs in the inner ear. Thus, we examined the inner ears of occludin-deficient (Occ(-/-)) mice. Although inner ears initially developed normally in Occ(-/-) mice, apoptosis occurs in hair cells in the organ of Corti around day 12 after birth, and deafness develops. Since hair cell degeneration was not observed in cochlear explant cultures of Occ(-/-) mice, environmental changes were considered to be the trigger of cell death. As for the vestibular system, both the morphologies and functions are normal in Occ(-/-) mice. These phenotypes of Occ(-/-) mice are very similar with those of claudin-14 or claudin-9 deficient mice, leading us to speculate on the existence of imbalance induced by TJ abnormalities, such as localized ionic components. Moreover, the occludin deficiency led to dislocalization of tricellulin, a gene responsible for human deafness DFNB49. The deafness in Occ(-/-) mice may be due to this dislocalization of tricellulin.
資源タイプ(コンテンツの種類)
ISSN
収録物識別子タイプ PISSN
収録物識別子 2046-6390
PubMed
識別子タイプ PMID
関連識別子 https://www.ncbi.nlm.nih.gov/pubmed/25063198
関連名称 25063198
権利
権利情報 © 2014. Published by The Company of Biologists Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
WoS
URL http://gateway.isiknowledge.com/gateway/Gateway.cgi?&GWVersion=2&SrcAuth=ShinshuUniv&SrcApp=ShinshuUniv&DestLinkType=FullRecord&DestApp=WOS&KeyUT=000348069900008
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Cite as

Kitajiri, Shin-ichiro, Katsuno, Tatsuya, Sasaki, Hiroyuki, Ito, Juichi, Furuse, Mikio, Tsukita, Shoichiro, 2014, Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells: COMPANY OF BIOLOGISTS LTD, 759–766 p.

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