Genetic insights into the morphogenesis of inner ear hair cells

The mammalian inner ear is a sensory organ that has specialized hair cells that detect sound, as well as orientation and movement of the head. The 'hair' bundle on the apical surface of these cells is a mechanosensitive organelle that consists of precisely organized actin-filled projections known as stereocilia. Alterations in hair-bundle morphogenesis can result in hearing loss, balance defects or both. Positional cloning of genes that underlie hereditary hearing loss, coupled with the characterization of corresponding mouse models, is revealing how hair cells have adapted the molecular mechanisms of intracellular motility and intercellular adhesion for the morphogenesis of their apical surfaces.

[1]  Ulrich Müller,et al.  The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Hackney,et al.  Cross-links between stereocilia in the guinea pig cochlea , 1985, Hearing Research.

[3]  K. Steel,et al.  Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D , 2001, Nature Genetics.

[4]  J. Rubin,et al.  Wnt signaling mediates reorientation of outer hair cell stereociliary bundles in the mammalian cochlea , 2003, Development.

[5]  S. Schwartz,et al.  Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. , 2001, Human molecular genetics.

[6]  J. Weber,et al.  A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17 , 1995, Nature Genetics.

[7]  T. N. Oliver,et al.  Tails of unconventional myosins , 1999, Cellular and Molecular Life Sciences CMLS.

[8]  D. DeRosier,et al.  The structure of the cuticular plate, an in vivo actin gel , 1989, The Journal of cell biology.

[9]  S. Tsukita,et al.  Cortical Actin Organization: Lessons from ERM (Ezrin/Radixin/Moesin) Proteins* , 1999, The Journal of Biological Chemistry.

[10]  L. Fananapazir,et al.  Mutations of MYO6 are associated with recessive deafness, DFNB37. , 2003, American journal of human genetics.

[11]  A J Hudspeth,et al.  DIRECTIONAL SENSITIVITY OF INDIVIDUAL VERTEBRATE HAIR CELLS TO CONTROLLED DEFLECTION OF THEIR HAIR BUNDLES * , 1981, Annals of the New York Academy of Sciences.

[12]  Mark E. Schneider,et al.  An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal , 2004, The Journal of cell biology.

[13]  G. Manley Cochlear mechanisms from a phylogenetic viewpoint. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[14]  J. T. Corwin,et al.  Stereociliary bundles reorient during hair cell development and regeneration in the chick cochlea , 1991, Hearing Research.

[15]  P. Sieving,et al.  PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. , 2003, Human molecular genetics.

[16]  Elaine Fuchs,et al.  Intercellular adhesion, signalling and the cytoskeleton , 2002, Nature Cell Biology.

[17]  A N Popper,et al.  Evolution of the ear and hearing: issues and questions. , 1997, Brain, behavior and evolution.

[18]  M. Charles Liberman,et al.  Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier , 2002, Nature.

[19]  N. Hirokawa,et al.  Interactions between actin filaments and between actin filaments and membranes in quick-frozen and deeply etched hair cells of the chick ear , 1982, The Journal of cell biology.

[20]  K. Steel,et al.  Role of myosin VI in the differentiation of cochlear hair cells. , 1999, Developmental biology.

[21]  E. Rubel,et al.  Mammalian vestibular hair cell regeneration , 1995, Science.

[22]  D. Drenckhahn,et al.  Sorting of actin isoforms in chicken auditory hair cells. , 1997, Journal of cell science.

[23]  D. DeRosier,et al.  Actin filaments, stereocilia, and hair cells of the bird cochlea. II. Packing of actin filaments in the stereocilia and in the cuticular plate and what happens to the organization when the stereocilia are bent , 1983, The Journal of cell biology.

[24]  Stephan C. Schuster,et al.  Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells , 2004, Nature.

[25]  J. Kaltenbach,et al.  Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles , 1994, The Journal of comparative neurology.

[26]  James A. Spudich,et al.  The Mechanism of Myosin VI Translocation and Its Load-Induced Anchoring , 2004, Cell.

[27]  M. Seeliger,et al.  Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D , 2001, Nature genetics.

[28]  J. T. Corwin,et al.  Ultrastructural evidence for hair cell regeneration in the mammalian inner ear. , 1993, Science.

[29]  J. Pickles,et al.  The development of links between stereocilia in hair cells of the chick basilar papilla , 1991, Hearing Research.

[30]  C. G. Wright,et al.  The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene , 2001, Nature Genetics.

[31]  E. Krieger,et al.  A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26) , 2003, Journal of medical genetics.

[32]  H. Ohmori,et al.  Mechano‐electrical transduction currents in isolated vestibular hair cells of the chick. , 1985, The Journal of physiology.

[33]  T. Friedman,et al.  A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25. , 2000, Genomics.

[34]  R. Romand,et al.  Fimbrin expression in the developing rat cochlea , 1995, Hearing Research.

[35]  D. DeRosier,et al.  Actin in the inner ear: the remarkable structure of the stereocilium , 1980, Nature.

[36]  Manfred Kössl,et al.  A Targeted Deletion in α-Tectorin Reveals that the Tectorial Membrane Is Required for the Gain and Timing of Cochlear Feedback , 2000, Neuron.

[37]  P. Gillespie,et al.  Developmental Assembly of Transduction Apparatus in Chick Basilar Papilla , 2003, The Journal of Neuroscience.

[38]  W. Gao,et al.  Immunocytochemical and Morphological Evidence for Intracellular Self-Repair as an Important Contributor to Mammalian Hair Cell Recovery , 1999, The Journal of Neuroscience.

[39]  E. H. Lambert,et al.  Hair cells in the inner ear of the pirouette and shaker 2 mutant mice , 2000, Journal of neurocytology.

[40]  Jing Zheng,et al.  Prestin is the motor protein of cochlear outer hair cells , 2000, Nature.

[41]  Y. Raphael,et al.  Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. , 1998, Science.

[42]  K. Steel,et al.  A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil , 2002, The European journal of neuroscience.

[43]  W. Lim,et al.  Mechanism and role of PDZ domains in signaling complex assembly. , 2001, Journal of cell science.

[44]  Daniel Safer,et al.  Myosin VI is an actin-based motor that moves backwards , 1999, Nature.

[45]  Winfried Denk,et al.  Calcium imaging of single stereocilia in hair cells: Localization of transduction channels at both ends of tip links , 1995, Neuron.

[46]  M. Kelley Cell adhesion molecules during inner ear and hair cell development, including notch and its ligands. , 2003, Current topics in developmental biology.

[47]  R. Goodyear,et al.  Distribution of the 275 kD hair cell antigen and cell surface specialisations on auditory and vestibular hair bundles in the chicken inner ear , 1992, The Journal of comparative neurology.

[48]  D. DeRosier,et al.  F-Actin Bundles Are Derivatives of Microvilli , 2000, The Journal of cell biology.

[49]  Steve D. M. Brown,et al.  Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 , 2003, Nature Genetics.

[50]  Julia Gorelik,et al.  Dynamic assembly of surface structures in living cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[51]  M. Deol The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse , 1956, Proceedings of the Royal Society of London. Series B - Biological Sciences.

[52]  A. J. Hudspeth,et al.  Ionic basis of the receptor potential in a vertebrate hair cell , 1979, Nature.

[53]  E. Mugnaini,et al.  The Deaf Jerker Mouse Has a Mutation in the Gene Encoding the Espin Actin-Bundling Proteins of Hair Cell Stereocilia and Lacks Espins , 2000, Cell.

[54]  M. King,et al.  Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. , 1997, Science.

[55]  Steve D. M. Brown,et al.  A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse , 2000, Nature Genetics.

[56]  Pierre Legrain,et al.  Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle , 2002, The EMBO journal.

[57]  Steve D. M. Brown,et al.  Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse , 2003, Current Biology.

[58]  C. Petit,et al.  Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. , 2003, Human molecular genetics.

[59]  Doris K. Wu,et al.  Revisiting cell fate specification in the inner ear , 2002, Current Opinion in Neurobiology.

[60]  M. Mlodzik,et al.  The atypical cadherin Flamingo links Frizzled and Notch signaling in planar polarity establishment in the Drosophila eye. , 2002, Developmental cell.

[61]  J. O. Pickles,et al.  Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction , 1984, Hearing Research.

[62]  H. Zoghbi,et al.  The role of Math1 in inner ear development: Uncoupling the establishment of the sensory primordium from hair cell fate determination. , 2002, Development.

[63]  Y. Raphael,et al.  Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice , 2001, Hearing Research.

[64]  John A. Assad,et al.  Tip-link integrity and mechanical transduction in vertebrate hair cells , 1991, Neuron.

[65]  T. Friedman,et al.  Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[66]  G. Richardson,et al.  Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment , 1998, Nature Genetics.

[67]  S. Ernstson,et al.  Stereo-kinociliar bonds in mammalian vestibular organs. , 1986, Acta oto-laryngologica.

[68]  R. Fay,et al.  Evolution of hearing in vertebrates: the inner ears and processing , 2000, Hearing Research.

[69]  A. Mansour,et al.  A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C , 2000, Nature Genetics.

[70]  H. Fuchs,et al.  Tailchaser (Tlc): A new mouse mutation affecting hair bundle differentiation and hair cell survival , 1999, Journal of neurocytology.

[71]  R. Nusse,et al.  Convergence of Wnt, ß-Catenin, and Cadherin Pathways , 2004, Science.

[72]  C. Morton,et al.  Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. , 1998, Science.

[73]  Sue Malcolm,et al.  A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene , 2000, Nature Genetics.

[74]  D. DeRosier,et al.  Actin filaments, stereocilia, and hair cells of the bird cochlea. IV. How the actin filaments become organized in developing stereocilia and in the cuticular plate. , 1986, Developmental biology.

[75]  C. G. Wright,et al.  A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15 , 2003, Hearing Research.

[76]  J. T. Corwin,et al.  Regenerative proliferation in inner ear sensory epithelia from adult guinea pigs and humans. , 1993, Science.

[77]  C. G. Wright,et al.  Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer , 2000, Hearing Research.

[78]  A. Griffith,et al.  Human nonsyndromic sensorineural deafness. , 2003, Annual review of genomics and human genetics.

[79]  J. Bartles Parallel actin bundles and their multiple actin-bundling proteins. , 2000, Current opinion in cell biology.

[80]  Karen P. Steel,et al.  The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells , 1995, Nature Genetics.

[81]  R. Goodyear,et al.  A Receptor-Like Inositol Lipid Phosphatase Is Required for the Maturation of Developing Cochlear Hair Bundles , 2003, The Journal of Neuroscience.

[82]  X. Estivill,et al.  MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. , 2001, American journal of human genetics.

[83]  G. Ehret Postnatal development in the acoustic system of the house mouse in the light of developing masked thresholds. , 1977, The Journal of the Acoustical Society of America.

[84]  K. Engel,et al.  Three different actin filament assemblies occur in every hair cell: each contains a specific actin crosslinking protein , 1991, The Journal of cell biology.

[85]  V. French,et al.  The long and the short of it , 1993, Nature.

[86]  D J DeRosier,et al.  Actin filaments, stereocilia, and hair cells: how cells count and measure. , 1992, Annual review of cell biology.

[87]  P. Gillespie,et al.  Regeneration of broken tip links and restoration of mechanical transduction in hair cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[88]  H. McNeill Sticking together and sorting things out: adhesion as a force in development , 2000, Nature Reviews Genetics.

[89]  Richard Goodyear,et al.  The Ankle-Link Antigen: an Epitope Sensitive to Calcium Chelation Associated with the Hair-Cell Surface and the Calycal Processes of Photoreceptors , 1999, The Journal of Neuroscience.

[90]  M. Ulfendahl,et al.  Actin-binding and microtubule-associated proteins in the organ of Corti , 1992, Hearing Research.

[91]  D. DeRosier,et al.  Actin Filaments , Stereocilia , and Hair Cells of the Bird Cochlea . V . How the Staircase Pattern of Stere iliary Lengths Is Generated , 2002 .

[92]  G. Richardson,et al.  The responses of cochlear hair cells to tonic displacements of the sensory hair bundle , 1989, Hearing Research.

[93]  A. Mitchell,et al.  Issues and questions , 2006 .

[94]  D. Corey,et al.  Unconventional Myosins in Inner-Ear Sensory Epithelia , 1997, The Journal of cell biology.

[95]  Niels Volkmann,et al.  An Atomic Model of Actin Filaments Cross-Linked by Fimbrin and Its Implications for Bundle Assembly and Function , 2001, The Journal of cell biology.

[96]  U. Wolfrum,et al.  Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex , 2000, The EMBO journal.

[97]  Peter Dallos,et al.  Prestin, a new type of motor protein , 2002, Nature Reviews Molecular Cell Biology.

[98]  S. Narumiya,et al.  Actin Polymerization-Driven Molecular Movement of mDia1 in Living Cells , 2004, Science.

[99]  Peter G. Gillespie,et al.  Cadherin 23 is a component of the tip link in hair-cell stereocilia , 2004, Nature.

[100]  A. Hudspeth Hair-bundle mechanics and a model for mechanoelectrical transduction by hair cells. , 1992, Society of General Physiologists series.

[101]  Marek Mlodzik,et al.  Planar cell polarization: do the same mechanisms regulate Drosophila tissue polarity and vertebrate gastrulation? , 2002, Trends in genetics : TIG.

[102]  A. Griffith,et al.  Stereocilia: the long and the short of it. , 2003, Trends in molecular medicine.

[103]  S. Riazuddin,et al.  Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. , 2001, American journal of human genetics.

[104]  K. Steel,et al.  Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. , 1998, Development.

[105]  M J Mulroy,et al.  The organization of actin filaments in the stereocilia of cochlear hair cells , 1980, The Journal of cell biology.

[106]  Steve D. M. Brown,et al.  Defective myosin VIIA gene responsible for Usher syndrome type IB , 1995, Nature.

[107]  D. Cotanche,et al.  Actin filaments, stereocilia and hair cells of the bird cochlea. VI. How the number and arrangement of stereocilia are determined. , 1992, Development.

[108]  G. Frolenkov,et al.  Expression and Localization of Prestin and the Sugar Transporter GLUT-5 during Development of Electromotility in Cochlear Outer Hair Cells , 2000, The Journal of Neuroscience.

[109]  A. Hudspeth,et al.  Radixin is a constituent of stereocilia in hair cells. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[110]  M. Wanger,et al.  Treadmilling of actin , 1983, Journal of Muscle Research & Cell Motility.

[111]  K. Steel,et al.  A type VII myosin encoded by the mouse deafness gene shaker-1 , 1995, Nature.

[112]  L. G. Tilney,et al.  Functional organization of the cytoskeleton , 1986, Hearing Research.

[113]  Stereociliary anomaly in the guinea pig: effects of hair bundle rotation on cochlear sensitivity , 1999, Hearing Research.

[114]  E. Mugnaini,et al.  Espin cross-links cause the elongation of microvillus-type parallel actin bundles in vivo , 2003, The Journal of cell biology.

[115]  N. Daudet,et al.  Transient expression of the t-isoform of plastins/fimbrin in the stereocilia of developing auditory hair cells. , 2002, Cell motility and the cytoskeleton.

[116]  J. R. Holt,et al.  Developmental acquisition of sensory transduction in hair cells of the mouse inner ear , 2003, Nature Neuroscience.

[117]  N. Copeland,et al.  Identification of Vangl2 and Scrb1 as planar polarity genes in mammals , 2003, Nature.

[118]  M. Tyska,et al.  MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells. , 2002, Biophysical journal.

[119]  S. Riazuddin,et al.  Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction , 2004, Journal of Medical Genetics.

[120]  Mark E. Schneider,et al.  Structural cell biology: Rapid renewal of auditory hair bundles , 2002, Nature.

[121]  Oliver Tn,et al.  Tails of unconventional myosins. , 1999 .

[122]  M. G. Evans,et al.  Fast adaptation of mechanoelectrical transducer channels in mammalian cochlear hair cells , 2003, Nature Neuroscience.

[123]  L. G. Tilney,et al.  Why Are Two Different Cross-linkers Necessary for Actin Bundle Formation In Vivo and What Does Each Cross-link Contribute? , 1998, The Journal of cell biology.

[124]  S. Leal,et al.  Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) , 2003 .

[125]  L. Fananapazir,et al.  Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6) , 2004, Journal of Medical Genetics.

[126]  R. Romand,et al.  Development of the auditory receptors of the rat: a SEM study , 1996, Brain Research.

[127]  Huawei Li,et al.  Correlation of expression of the actin filament‐bundling protein espin with stereociliary bundle formation in the developing inner ear , 2004, The Journal of comparative neurology.

[128]  E. Bearer,et al.  2E4 (kaptin): a novel actin-associated protein from human blood platelets found in lamellipodia and the tips of the stereocilia of the inner ear. , 1999, European journal of cell biology.

[129]  K. Verhoeven Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment , 1999, Nature Genetics.

[130]  C. Cepko,et al.  The chicken RaxL gene plays a role in the initiation of photoreceptor differentiation , 2002, Development.

[131]  M. Bitner-Glindzicz,et al.  Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. , 2001, American journal of human genetics.

[132]  T. Mitchison,et al.  Regulated Actin Cytoskeleton Assembly at Filopodium Tips Controls Their Extension and Retraction , 1999, The Journal of cell biology.