Literature DB >> 7825434

Gap junction systems in the rat vestibular labyrinth: immunohistochemical and ultrastructural analysis.

T Kikuchi1, J C Adams, D L Paul, R S Kimura.   

Abstract

The distribution of gap junctions within the vestibular labyrinth was investigated using immunohistochemistry and transmission electron microscopy. Connexin26-like immunoreactivity was observed among supporting cells in each vestibular sensory epithelium. Reaction product was also present in the transitional epithelium of each vestibular endorgan and in the planum semilunatum of crista ampullaris. No connexin26-like immunoreactivity was observed among thin wall epithelial cells or among vestibular dark cells. In addition, fibrocytes within vestibular connective tissue were positively immunostained. Reaction product was also detected in the melanocyte area just beneath dark cells. Ultrastructural observations indicated that a gap junction network of vestibular supporting cells extends to the transitional epithelium and planum semilunatum and forms an isolated epithelial cell gap junction system in each vestibular endorgan. In contrast, no gap junctions were found among wall epithelial cells or among dark cells. Fibrocytes and melanocytes were coupled by gap junctions and belong to the connective tissue cell gap junction system, which is continuous throughout the vestibular system and the cochlea. The possible functional significance of these gap junction systems is discussed.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7825434     DOI: 10.3109/00016489409126097

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  14 in total

Review 1.  Purinergic signaling in the inner ear.

Authors:  Jun Ho Lee; Daniel C Marcus
Journal:  Hear Res       Date:  2007-09-29       Impact factor: 3.208

2.  Vestibular dysfunction in DFNB1 deafness.

Authors:  Kelley M Dodson; Susan H Blanton; Katherine O Welch; Virginia W Norris; Regina L Nuzzo; Jacob A Wegelin; Ruth S Marin; Walter E Nance; Arti Pandya; Kathleen S Arnos
Journal:  Am J Med Genet A       Date:  2011-04-04       Impact factor: 2.802

3.  Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.

Authors:  Martine Cohen-Salmon; Thomas Ott; Vincent Michel; Jean Pierre Hardelin; Isabelle Perfettini; Michel Eybalin; Tao Wu; Daniel C Marcus; Philine Wangemann; Klaus Willecke; Christine Petit
Journal:  Curr Biol       Date:  2002-07-09       Impact factor: 10.834

Review 4.  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

5.  Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

Authors:  Gülistan Meşe; Eric Londin; Rickie Mui; Peter R Brink; Thomas W White
Journal:  Hum Genet       Date:  2004-07-07       Impact factor: 4.132

6.  Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear.

Authors:  Saida Ortolano; Giovanni Di Pasquale; Giulia Crispino; Fabio Anselmi; Fabio Mammano; John A Chiorini
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-01       Impact factor: 11.205

Review 7.  Cellular targeting for cochlear gene therapy.

Authors:  Allen F Ryan; Lina M Mullen; Joni K Doherty
Journal:  Adv Otorhinolaryngol       Date:  2009-06-02

8.  Analysis of connexin subunits required for the survival of vestibular hair cells.

Authors:  Yan Qu; Wenxue Tang; Ian Dahlke; Dalian Ding; Richard Salvi; Goran Söhl; Klaus Willecke; Ping Chen; Xi Lin
Journal:  J Comp Neurol       Date:  2007-10-10       Impact factor: 3.215

9.  Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.

Authors:  Ines E Royaux; Inna A Belyantseva; Tao Wu; Bechara Kachar; Lorraine A Everett; Daniel C Marcus; Eric D Green
Journal:  J Assoc Res Otolaryngol       Date:  2003-09

10.  A novel missense mutation in the connexin30 causes nonsyndromic hearing loss.

Authors:  Wen-Hung Wang; Yu-Fan Liu; Ching-Chyuan Su; Mao-Chang Su; Shuan-Yow Li; Jiann-Jou Yang
Journal:  PLoS One       Date:  2011-06-24       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.