Literature DB >> 17567809

Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.

Nicolas Michalski1, Vincent Michel, Amel Bahloul, Gaëlle Lefèvre, Jérémie Barral, Hideshi Yagi, Sébastien Chardenoux, Dominique Weil, Pascal Martin, Jean-Pierre Hardelin, Makoto Sato, Christine Petit.   

Abstract

Several lines of evidence indicate that very large G-protein-coupled receptor 1 (Vlgr1) makes up the ankle links that connect the stereocilia of hair cells at their base. Here, we show that the transmembrane protein usherin, the putative transmembrane protein vezatin, and the PDZ (postsynaptic density-95/Discs large/zona occludens-1) domain-containing submembrane protein whirlin are colocalized with Vlgr1 at the stereocilia base in developing cochlear hair cells and are absent in Vlgr1-/- mice that lack the ankle links. Direct in vitro interactions between these four proteins further support their involvement in a molecular complex associated with the ankle links and scaffolded by whirlin. In addition, the delocalization of these proteins in myosin VIIa defective mutant mice as well as the myosin VIIa tail direct interactions with vezatin, whirlin, and, we show, Vlgr1 and usherin, suggest that myosin VIIa conveys proteins of the ankle-link complex to the stereocilia. Adenylyl cyclase 6, which was found at the base of stereocilia, was both overexpressed and mislocated in Vlgr1-/- mice. In postnatal day 7 Vlgr1-/- mice, mechanoelectrical transduction currents evoked by displacements of the hair bundle toward the tallest stereocilia (i.e., in the excitatory direction) were reduced in outer but not inner hair cells. In both cell types, stimulation of the hair bundle in the opposite direction paradoxically resulted in significant transduction currents. The absence of ankle-link-mediated cohesive forces within hair bundles lacking Vlgr1 may account for the electrophysiological results. However, because some long cadherin-23 isoforms could no longer be detected in Vlgr1-/- mice shortly after birth, the loss of some apical links could be involved too. The premature disappearance of these cadherin isoforms in the Vlgr1-/- mutant argues in favor of a signaling function of the ankle links in hair bundle differentiation.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17567809      PMCID: PMC6672440          DOI: 10.1523/JNEUROSCI.0342-07.2007

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  51 in total

1.  Expression pattern of adenylyl cyclase isoforms in the inner ear of the rat by RT-PCR and immunochemical localization of calcineurin in the organ of Corti.

Authors:  H Kumagami; E Beitz; K Wild; H P Zenner; J P Ruppersberg; J E Schultz
Journal:  Hear Res       Date:  1999-06       Impact factor: 3.208

2.  The ankle-link antigen: an epitope sensitive to calcium chelation associated with the hair-cell surface and the calycal processes of photoreceptors.

Authors:  R Goodyear; G Richardson
Journal:  J Neurosci       Date:  1999-05-15       Impact factor: 6.167

3.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

Authors:  J M Bork; L M Peters; S Riazuddin; S L Bernstein; Z M Ahmed; S L Ness; R Polomeno; A Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Z Ahmed; S N Khan; V M Kaloustian; X C Li; A Lalwani; S Riazuddin; M Bitner-Glindzicz; W E Nance; X Z Liu; G Wistow; R J Smith; A J Griffith; E R Wilcox; T B Friedman; R J Morell
Journal:  Am J Hum Genet       Date:  2000-11-21       Impact factor: 11.025

4.  Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.

Authors:  C J Kros; W Marcotti; S M van Netten; T J Self; R T Libby; S D M Brown; G P Richardson; K P Steel
Journal:  Nat Neurosci       Date:  2002-01       Impact factor: 24.884

5.  Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.

Authors:  H Bolz; B von Brederlow; A Ramírez; E C Bryda; K Kutsche; H G Nothwang; M Seeliger; M del C-Salcedó Cabrera; M C Vila; O P Molina; A Gal; C Kubisch
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

6.  Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

Authors:  Z M Ahmed; S Riazuddin; S L Bernstein; Z Ahmed; S Khan; A J Griffith; R J Morell; T B Friedman; S Riazuddin; E R Wilcox
Journal:  Am J Hum Genet       Date:  2001-06-07       Impact factor: 11.025

7.  Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

Authors:  K N Alagramam; H Yuan; M H Kuehn; C L Murcia; S Wayne; C R Srisailpathy; R B Lowry; R Knaus; L Van Laer; F P Bernier; S Schwartz; C Lee; C C Morton; R F Mullins; A Ramesh; G Van Camp; G S Hageman; R P Woychik; R J Smith; G S Hagemen
Journal:  Hum Mol Genet       Date:  2001-08-01       Impact factor: 6.150

8.  Unconventional myosin VIIA is a novel A-kinase-anchoring protein.

Authors:  P Küssel-Andermann; A El-Amraoui; S Safieddine; J P Hardelin; S Nouaille; J Camonis; C Petit
Journal:  J Biol Chem       Date:  2000-09-22       Impact factor: 5.157

9.  Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex.

Authors:  P Küssel-Andermann; A El-Amraoui; S Safieddine; S Nouaille; I Perfettini; M Lecuit; P Cossart; U Wolfrum; C Petit
Journal:  EMBO J       Date:  2000-11-15       Impact factor: 11.598

10.  Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system.

Authors:  D Randy McMillan; Kathleen M Kayes-Wandover; James A Richardson; Perrin C White
Journal:  J Biol Chem       Date:  2001-10-17       Impact factor: 5.157

View more
  104 in total

1.  Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells.

Authors:  Maryline Beurg; Nicolas Michalski; Saaid Safieddine; Yohan Bouleau; Ralf Schneggenburger; Edwin R Chapman; Christine Petit; Didier Dulon
Journal:  J Neurosci       Date:  2010-10-06       Impact factor: 6.167

2.  Development and regeneration of sensory transduction in auditory hair cells requires functional interaction between cadherin-23 and protocadherin-15.

Authors:  Andrea Lelli; Piotr Kazmierczak; Yoshiyuki Kawashima; Ulrich Müller; Jeffrey R Holt
Journal:  J Neurosci       Date:  2010-08-25       Impact factor: 6.167

Review 3.  Genetics and pathological mechanisms of Usher syndrome.

Authors:  Denise Yan; Xue Z Liu
Journal:  J Hum Genet       Date:  2010-04-09       Impact factor: 3.172

4.  Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.

Authors:  Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Riazuddin; Thomas B Friedman
Journal:  Am J Hum Genet       Date:  2010-02-18       Impact factor: 11.025

5.  Sensory transduction and adaptation in inner and outer hair cells of the mouse auditory system.

Authors:  Eric A Stauffer; Jeffrey R Holt
Journal:  J Neurophysiol       Date:  2007-10-17       Impact factor: 2.714

6.  Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.

Authors:  Marisa Zallocchi; Duane Delimont; Daniel T Meehan; Dominic Cosgrove
Journal:  J Neurosci       Date:  2012-10-03       Impact factor: 6.167

7.  CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI.

Authors:  Felipe T Salles; Leonardo R Andrade; Soichi Tanda; M'hamed Grati; Kathleen L Plona; Leona H Gagnon; Kenneth R Johnson; Bechara Kachar; Mark A Berryman
Journal:  Cytoskeleton (Hoboken)       Date:  2013-12-10

Review 8.  Inheritance patterns of progressive hearing loss in laboratory strains of mice.

Authors:  Konrad Noben-Trauth; Kenneth R Johnson
Journal:  Brain Res       Date:  2009-02-21       Impact factor: 3.252

Review 9.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

Review 10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.