Literature DB >> 30638948

Building and repairing the stereocilia cytoskeleton in mammalian auditory hair cells.

A Catalina Vélez-Ortega1, Gregory I Frolenkov2.   

Abstract

Despite all recent achievements in identification of the molecules that are essential for the structure and mechanosensory function of stereocilia bundles in the auditory hair cells of mammalian species, we still have only a rudimentary understanding of the mechanisms of stereocilia formation, maintenance, and repair. Important molecular differences distinguishing mammalian auditory hair cells from hair cells of other types and species have been recently revealed. In addition, we are beginning to solve the puzzle of the apparent life-long stability of the stereocilia bundles in these cells. New data link the stability of the cytoskeleton in the mammalian auditory stereocilia with the normal activity of mechanotransduction channels. These data suggest new ideas on how a terminally-differentiated non-regenerating hair cell in the mammalian cochlea may repair and tune its stereocilia bundle throughout the life span of the organism.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Actin; Deafness; Inner ear hair cells; Mechanotransduction; Noise

Year:  2019        PMID: 30638948      PMCID: PMC6456422          DOI: 10.1016/j.heares.2018.12.012

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  140 in total

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Review 2.  Filamins in mechanosensing and signaling.

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3.  Correlation of actin crosslinker and capper expression levels with stereocilia growth phases.

Authors:  Matthew R Avenarius; Katherine W Saylor; Megan R Lundeberg; Phillip A Wilmarth; Jung-Bum Shin; Kateri J Spinelli; James M Pagana; Leonardo Andrade; Bechara Kachar; Dongseok Choi; Larry L David; Peter G Barr-Gillespie
Journal:  Mol Cell Proteomics       Date:  2013-12-07       Impact factor: 5.911

4.  Non-muscle alpha actinins are calcium-sensitive actin-binding proteins.

Authors:  K Burridge; J R Feramisco
Journal:  Nature       Date:  1981-12-10       Impact factor: 49.962

5.  An immunogold investigation of the distribution of calmodulin in the apex of cochlear hair cells.

Authors:  D N Furness; A Karkanevatos; B West; C M Hackney
Journal:  Hear Res       Date:  2002-11       Impact factor: 3.208

6.  Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.

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Journal:  Hum Mol Genet       Date:  2003-03-01       Impact factor: 6.150

7.  Plasma membrane Ca2+-ATPase extrudes Ca2+ from hair cell stereocilia.

Authors:  E N Yamoah; E A Lumpkin; R A Dumont; P J Smith; A J Hudspeth; P G Gillespie
Journal:  J Neurosci       Date:  1998-01-15       Impact factor: 6.167

8.  Mutation analysis of the mouse myosin VIIA deafness gene.

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Journal:  Genes Funct       Date:  1997-06

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Authors:  C S Lin; W Shen; Z P Chen; Y H Tu; P Matsudaira
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10.  Heterodimeric capping protein is required for stereocilia length and width regulation.

Authors:  Matthew R Avenarius; Jocelyn F Krey; Rachel A Dumont; Clive P Morgan; Connor B Benson; Sarath Vijayakumar; Christopher L Cunningham; Deborah I Scheffer; David P Corey; Ulrich Müller; Sherri M Jones; Peter G Barr-Gillespie
Journal:  J Cell Biol       Date:  2017-09-12       Impact factor: 8.077

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  9 in total

1.  Rbm24 regulates inner-ear-specific alternative splicing and is essential for maintaining auditory and motor coordination.

Authors:  Longqing Zheng; Huijun Yuan; Mengkai Zhang; Cuicui Wang; Xuemin Cai; Jing Liu; Xiu Qin Xu
Journal:  RNA Biol       Date:  2020-09-20       Impact factor: 4.652

Review 2.  The many roles of myosins in filopodia, microvilli and stereocilia.

Authors:  Anne Houdusse; Margaret A Titus
Journal:  Curr Biol       Date:  2021-05-24       Impact factor: 10.900

Review 3.  Functional Role of Class III Myosins in Hair Cells.

Authors:  Joseph A Cirilo; Laura K Gunther; Christopher M Yengo
Journal:  Front Cell Dev Biol       Date:  2021-02-25

4.  Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells.

Authors:  Beatriz Lorente-Cánovas; Stephanie Eckrich; Morag A Lewis; Stuart L Johnson; Walter Marcotti; Karen P Steel
Journal:  PLoS One       Date:  2022-03-02       Impact factor: 3.240

5.  BAIAP2L2 Inactivation Does Not Affect Stereocilia Development or Maintenance in Vestibular Hair Cells.

Authors:  Keji Yan; Chengli Qu; Yanfei Wang; Wen Zong; Zhigang Xu
Journal:  Front Mol Neurosci       Date:  2022-02-15       Impact factor: 5.639

6.  AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafness.

Authors:  Jing-Yi Jeng; Adam J Carlton; Richard J Goodyear; Colbie Chinowsky; Federico Ceriani; Stuart L Johnson; Tsung-Chang Sung; Yelena Dayn; Guy P Richardson; Michael R Bowl; Steve D M Brown; Uri Manor; Walter Marcotti
Journal:  Mol Ther Methods Clin Dev       Date:  2022-07-31       Impact factor: 5.849

Review 7.  Growth factor and receptor malfunctions associated with human genetic deafness.

Authors:  Sadaf Naz; Thomas B Friedman
Journal:  Clin Genet       Date:  2019-10-23       Impact factor: 4.296

8.  Multiple PDZ domain protein maintains patterning of the apical cytoskeleton in sensory hair cells.

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Journal:  Development       Date:  2021-07-21       Impact factor: 6.862

9.  Loss of Baiap2l2 destabilizes the transducing stereocilia of cochlear hair cells and leads to deafness.

Authors:  Adam J Carlton; Julia Halford; Anna Underhill; Jing-Yi Jeng; Matthew R Avenarius; Merle L Gilbert; Federico Ceriani; Kimimuepigha Ebisine; Steve D M Brown; Michael R Bowl; Peter G Barr-Gillespie; Walter Marcotti
Journal:  J Physiol       Date:  2020-11-26       Impact factor: 5.182

  9 in total

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