Literature DB >> 14986102

Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.

Martine Cohen-Salmon1, Stephan Maxeiner, Olaf Krüger, Martin Theis, Klaus Willecke, Christine Petit.   

Abstract

Intercellular communication through gap junctions is crucial for proper functioning of the inner ear. Indeed, mutations in several connexin genes have been found to cause hearing loss. In the inner ear, only the cell distributions of connexin30 and connexin26 have been well documented. We took advantage of the lacZ reporter gene in Cx43 and Cx45 knock-out mice to study the expression of the connexin43 and connexin45 genes during the inner ear development. Expression of Cx43 and Cx45 in the inner ear was detected from embryonic days 15.5 and 17.5, respectively. Until the 1st week of life, Cx43 was highly expressed in the connective tissues, and weakly expressed in the immature sensory epithelium of the cochlea. From postnatal day 8, however, Cx43 was almost exclusively expressed in the bone of the otic capsule. During embryogenesis, Cx45 was expressed in epithelial and connective inner ear tissues. From birth onwards, Cx45 expression could be detected in some inner ear capillaries. Vascular expression thereafter increased and persisted in the adult. In the mature inner ear, Cx45 was expressed in the entire vasculature. These results indicate that connexin43 and connexin45 play a role in the otic capsule bone and the inner ear vascular system, respectively.

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Year:  2004        PMID: 14986102     DOI: 10.1007/s00441-004-0861-2

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  28 in total

Review 1.  Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential.

Authors:  Philine Wangemann
Journal:  J Physiol       Date:  2006-07-20       Impact factor: 5.182

2.  Compartmentalized and signal-selective gap junctional coupling in the hearing cochlea.

Authors:  Daniel J Jagger; Andrew Forge
Journal:  J Neurosci       Date:  2006-01-25       Impact factor: 6.167

Review 3.  Emerging roles of pericytes in the regulation of the neurovascular unit in health and disease.

Authors:  Jeremy Hill; Slava Rom; Servio H Ramirez; Yuri Persidsky
Journal:  J Neuroimmune Pharmacol       Date:  2014-08-14       Impact factor: 4.147

Review 4.  Gap junctions and cochlear homeostasis.

Authors:  H-B Zhao; T Kikuchi; A Ngezahayo; T W White
Journal:  J Membr Biol       Date:  2006-05-17       Impact factor: 1.843

Review 5.  Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Authors:  Emilie Hoang Dinh; Shoeb Ahmad; Qing Chang; Wenxue Tang; Benjamin Stong; Xi Lin
Journal:  Brain Res       Date:  2009-02-20       Impact factor: 3.252

6.  Connexin45 regulates endothelial-induced mesenchymal cell differentiation toward a mural cell phenotype.

Authors:  Jennifer S Fang; Cuiping Dai; David T Kurjiaka; Janis M Burt; Karen K Hirschi
Journal:  Arterioscler Thromb Vasc Biol       Date:  2012-12-06       Impact factor: 8.311

7.  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

8.  Pannexins are new molecular candidates for assembling gap junctions in the cochlea.

Authors:  Wenxue Tang; Shoeb Ahmad; Valery I Shestopalov; Xi Lin
Journal:  Neuroreport       Date:  2008-08-27       Impact factor: 1.837

9.  Connexin29 is highly expressed in cochlear Schwann cells, and it is required for the normal development and function of the auditory nerve of mice.

Authors:  Wenxue Tang; Yanping Zhang; Qing Chang; Shoab Ahmad; Ian Dahlke; Hong Yi; Ping Chen; David L Paul; Xi Lin
Journal:  J Neurosci       Date:  2006-02-15       Impact factor: 6.167

10.  Connexin26 deafness associated mutations show altered permeability to large cationic molecules.

Authors:  Gülistan Meşe; Virginijus Valiunas; Peter R Brink; Thomas W White
Journal:  Am J Physiol Cell Physiol       Date:  2008-08-06       Impact factor: 4.249

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