Literature DB >> 16703388

Distribution of pendrin in the organ of Corti of mice observed by electron immunomicroscopy.

Takahiko Yoshino1, Eisuke Sato, Tsutomu Nakashima, Masaaki Teranishi, Hiroshi Yamamoto, Hironao Otake, Terukazu Mizuno.   

Abstract

The distribution of pendrin, which is encoded by the Pendred syndrome gene, has been investigated immunohistochemically in the inner ear. In the cochlea, pendrin has been found in the spiral prominence, external sulcus cells, Hensen's cells and Claudius cells, but its expression in the organ of Corti remains unclear. We examined whether pendrin localizes in the organ of Corti by postembedding immunogold analysis. In the organ of Corti, gold particles were clearly observed in outer and inner hair cells, including the stereocilia. The density of the particles was especially high in the cuticular plates of the hair cells. Gold particles were also detected in the external sulcus, in part of the spiral ligament adjacent to the external sulcus, in supporting cells, and in the spiral ganglion of the cochlea. Our study revealed that pendrin occurs in the organ of Corti. The role of pendrin in the organ of Corti and its association with the Cl- or pH regulation of neurotransmission require further study.

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Year:  2006        PMID: 16703388     DOI: 10.1007/s00405-006-0045-7

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  25 in total

1.  Prestin is the motor protein of cochlear outer hair cells.

Authors:  J Zheng; W Shen; D Z He; K B Long; L D Madison; P Dallos
Journal:  Nature       Date:  2000-05-11       Impact factor: 49.962

Review 2.  Production of inner ear fluids.

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Journal:  Physiol Rev       Date:  1988-10       Impact factor: 37.312

3.  Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

Authors:  L A Everett; I A Belyantseva; K Noben-Trauth; R Cantos; A Chen; S I Thakkar; S L Hoogstraten-Miller; B Kachar; D K Wu; E D Green
Journal:  Hum Mol Genet       Date:  2001-01-15       Impact factor: 6.150

4.  Electrokinetic shape changes of cochlear outer hair cells.

Authors:  B Kachar; W E Brownell; R Altschuler; J Fex
Journal:  Nature       Date:  1986 Jul 24-30       Impact factor: 49.962

5.  Evoked mechanical responses of isolated cochlear outer hair cells.

Authors:  W E Brownell; C R Bader; D Bertrand; Y de Ribaupierre
Journal:  Science       Date:  1985-01-11       Impact factor: 47.728

6.  Plasmalemmal ATPase calcium pump localizes to inner and outer hair bundles.

Authors:  S Apicella; S Chen; R Bing; J T Penniston; R Llinas; D E Hillman
Journal:  Neuroscience       Date:  1997-08       Impact factor: 3.590

7.  The Pendred syndrome gene encodes a chloride-iodide transport protein.

Authors:  D A Scott; R Wang; T M Kreman; V C Sheffield; L P Karniski
Journal:  Nat Genet       Date:  1999-04       Impact factor: 38.330

8.  Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).

Authors:  L A Everett; B Glaser; J C Beck; J R Idol; A Buchs; M Heyman; F Adawi; E Hazani; E Nassir; A D Baxevanis; V C Sheffield; E D Green
Journal:  Nat Genet       Date:  1997-12       Impact factor: 38.330

9.  The immunohistochemical analysis of pendrin in the mouse inner ear.

Authors:  Takahiko Yoshino; Eisuke Sato; Tsutomu Nakashima; Wataru Nagashima; Masa-Aki Teranishi; Atsuo Nakayama; Naoyoshi Mori; Hideki Murakami; Hiroomi Funahashi; Tsuneo Imai
Journal:  Hear Res       Date:  2004-09       Impact factor: 3.208

10.  Experience-dependent changes in intracellular Cl- regulation in developing auditory neurons.

Authors:  Shumei Shibata; Yasuhiro Kakazu; Akihito Okabe; Atsuo Fukuda; Junichi Nabekura
Journal:  Neurosci Res       Date:  2004-02       Impact factor: 3.304

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  10 in total

1.  Immunohistochemical localization of megalin and cubilin in the human inner ear.

Authors:  Seiji Hosokawa; Kumiko Hosokawa; Gail Ishiyama; Akira Ishiyama; Ivan A Lopez
Journal:  Brain Res       Date:  2018-09-12       Impact factor: 3.252

2.  LMO4 functions as a negative regulator of sensory organ formation in the mammalian cochlea.

Authors:  Min Deng; Xiong-jian Luo; Ling Pan; Hua Yang; Xiaoling Xie; Guoqing Liang; Liang Huang; Fang Hu; Amy E Kiernan; Lin Gan
Journal:  J Neurosci       Date:  2014-07-23       Impact factor: 6.167

Review 3.  Function and expression pattern of nonsyndromic deafness genes.

Authors:  Nele Hilgert; Richard J H Smith; Guy Van Camp
Journal:  Curr Mol Med       Date:  2009-06       Impact factor: 2.222

4.  A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China.

Authors:  Junzhen Zhu; Qinying Cao; Ning Zhang; Jun Ge; Donglan Sun; Qingqi Feng
Journal:  Intractable Rare Dis Res       Date:  2015-08

5.  Cochlear dysfunction in patients with acute hypothyroidism.

Authors:  Vassilis Psaltakos; Dimitrios G Balatsouras; Ioannis Sengas; Eleftherios Ferekidis; Maria Riga; Stavros G Korres
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-12-25       Impact factor: 2.503

6.  Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.

Authors:  Filiz Basak Cengiz; Rasim Yilmazer; Levent Olgun; Levent Sennaroglu; Tayfun Kirazli; Hudaver Alper; Yuksel Olgun; Armagan Incesulu; Tahir Atik; Fabiola Huesca-Hernandez; Juan Domínguez-Aburto; Garly González-Rosado; Edgar Hernandez-Zamora; Maria de la Luz Arenas-Sordo; Ibis Menendez; Kadir Serkan Orhan; Hakan Avci; Nejat Mahdieh; Mortaza Bonyadi; Joseph Foster; Duygu Duman; Ferda Ozkinay; Susan H Blanton; Guney Bademci; Mustafa Tekin
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2017-08-08       Impact factor: 1.675

7.  Two common and three novel PDS mutations in Thai patients with Pendred syndrome.

Authors:  T Snabboon; W Plengpanich; S Saengpanich; S Sirisalipoch; S Keelawat; S Sunthornyothin; W Khovidhunkit; S Suwanwalaikorn; V Sridama; V Shotelersuk
Journal:  J Endocrinol Invest       Date:  2007-12       Impact factor: 4.256

Review 8.  Autosomal recessive nonsyndromic deafness genes: a review.

Authors:  Duygu Duman; Mustafa Tekin
Journal:  Front Biosci (Landmark Ed)       Date:  2012-06-01

9.  Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.

Authors:  Fatima Ammar-Khodja; Crystel Bonnet; Malika Dahmani; Sofiane Ouhab; Gaelle M Lefèvre; Hassina Ibrahim; Jean-Pierre Hardelin; Dominique Weil; Malek Louha; Christine Petit
Journal:  Mol Genet Genomic Med       Date:  2015-02-15       Impact factor: 2.183

Review 10.  The Roles of Solute Carriers in Auditory Function.

Authors:  Fuping Qian; Xiaoge Jiang; Renjie Chai; Dong Liu
Journal:  Front Genet       Date:  2022-01-26       Impact factor: 4.599

  10 in total

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