Literature DB >> 22177415

Sensing sound: molecules that orchestrate mechanotransduction by hair cells.

Piotr Kazmierczak1, Ulrich Müller.   

Abstract

Animals use acoustic signals to communicate and to obtain information about their environment. The processing of acoustic signals is initiated at auditory sense organs, where mechanosensory hair cells convert sound-induced vibrations into electrical signals. Although the biophysical principles underlying the mechanotransduction process in hair cells have been characterized in much detail over the past 30 years, the molecular building-blocks of the mechanotransduction machinery have proved to be difficult to determine. We review here recent studies that have both identified some of these molecules and established the mechanisms by which they regulate the activity of the still-elusive mechanotransduction channel.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22177415      PMCID: PMC3310959          DOI: 10.1016/j.tins.2011.10.007

Source DB:  PubMed          Journal:  Trends Neurosci        ISSN: 0166-2236            Impact factor:   13.837


  116 in total

1.  High-resolution structure of hair-cell tip links.

Authors:  B Kachar; M Parakkal; M Kurc; Y Zhao; P G Gillespie
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

2.  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

3.  A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata.

Authors:  T Wada; Y Wakabayashi; S Takahashi; T Ushiki; Y Kikkawa; H Yonekawa; R Kominami
Journal:  Biochem Biophys Res Commun       Date:  2001-04-27       Impact factor: 3.575

4.  Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

Authors:  F Di Palma; R H Holme; E C Bryda; I A Belyantseva; R Pellegrino; B Kachar; K P Steel; K Noben-Trauth
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

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.  The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.

Authors:  K N Alagramam; C L Murcia; H Y Kwon; K S Pawlowski; C G Wright; R P Woychik
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

7.  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

8.  A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.

Authors:  E Verpy; M Leibovici; I Zwaenepoel; X Z Liu; A Gal; N Salem; A Mansour; S Blanchard; I Kobayashi; B J Keats; R Slim; C Petit
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

9.  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

10.  Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.

Authors:  S M Wilson; D B Householder; V Coppola; L Tessarollo; B Fritzsch; E C Lee; D Goss; G A Carlson; N G Copeland; N A Jenkins
Journal:  Genomics       Date:  2001-06-01       Impact factor: 5.736

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  32 in total

1.  Lis1 mediates planar polarity of auditory hair cells through regulation of microtubule organization.

Authors:  Conor W Sipe; Lixia Liu; Jianyi Lee; Cynthia Grimsley-Myers; Xiaowei Lu
Journal:  Development       Date:  2013-04       Impact factor: 6.868

2.  TMC1 Forms the Pore of Mechanosensory Transduction Channels in Vertebrate Inner Ear Hair Cells.

Authors:  Bifeng Pan; Nurunisa Akyuz; Xiao-Ping Liu; Yukako Asai; Carl Nist-Lund; Kiyoto Kurima; Bruce H Derfler; Bence György; Walrati Limapichat; Sanket Walujkar; Lahiru N Wimalasena; Marcos Sotomayor; David P Corey; Jeffrey R Holt
Journal:  Neuron       Date:  2018-08-22       Impact factor: 17.173

3.  Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function.

Authors:  Wei-Zheng Zeng; Nicolas Grillet; James B Dewey; Alix Trouillet; Jocelyn F Krey; Peter G Barr-Gillespie; John S Oghalai; Ulrich Müller
Journal:  J Neurosci       Date:  2016-08-31       Impact factor: 6.167

4.  Genomic architecture of Shh-dependent cochlear morphogenesis.

Authors:  Victor Muthu; Alex M Rohacek; Yao Yao; Staci M Rakowiecki; Alexander S Brown; Ying-Tao Zhao; James Meyers; Kyoung-Jae Won; Shweta Ramdas; Christopher D Brown; Kevin A Peterson; Douglas J Epstein
Journal:  Development       Date:  2019-09-19       Impact factor: 6.868

5.  Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.

Authors:  Atteeq U Rehman; Regie Lyn P Santos-Cortez; Robert J Morell; Meghan C Drummond; Taku Ito; Kwanghyuk Lee; Asma A Khan; Muhammad Asim R Basra; Naveed Wasif; Muhammad Ayub; Rana A Ali; Syed I Raza; Deborah A Nickerson; Jay Shendure; Michael Bamshad; Saima Riazuddin; Neil Billington; Shaheen N Khan; Penelope L Friedman; Andrew J Griffith; Wasim Ahmad; Sheikh Riazuddin; Suzanne M Leal; Thomas B Friedman
Journal:  Am J Hum Genet       Date:  2014-01-02       Impact factor: 11.025

6.  A molecular level prototype for mechanoelectrical transducer in mammalian hair cells.

Authors:  Jinkyoung Park; Guo-Wei Wei
Journal:  J Comput Neurosci       Date:  2013-04-28       Impact factor: 1.621

7.  Global Analysis of Protein Expression of Inner Ear Hair Cells.

Authors:  Ann E Hickox; Ann C Y Wong; Kwang Pak; Chelsee Strojny; Miguel Ramirez; John R Yates; Allen F Ryan; Jeffrey N Savas
Journal:  J Neurosci       Date:  2016-12-30       Impact factor: 6.167

8.  ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.

Authors:  Alex M Rohacek; Thomas W Bebee; Richard K Tilton; Caleb M Radens; Chris McDermott-Roe; Natoya Peart; Maninder Kaur; Michael Zaykaner; Benjamin Cieply; Kiran Musunuru; Yoseph Barash; John A Germiller; Ian D Krantz; Russ P Carstens; Douglas J Epstein
Journal:  Dev Cell       Date:  2017-10-26       Impact factor: 12.270

Review 9.  Function and Dysfunction of TMC Channels in Inner Ear Hair Cells.

Authors:  David P Corey; Nurunisa Akyuz; Jeffrey R Holt
Journal:  Cold Spring Harb Perspect Med       Date:  2019-10-01       Impact factor: 6.915

Review 10.  The elusive mechanotransduction machinery of hair cells.

Authors:  Bo Zhao; Ulrich Müller
Journal:  Curr Opin Neurobiol       Date:  2015-09-03       Impact factor: 6.627

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