The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development
Open Access
- 26 February 2007
- journal article
- research article
- Published by Wiley in Cell Motility
- Vol. 64 (7) , 496-508
- https://doi.org/10.1002/cm.20199
Abstract
Stereocilia, finger-like projections forming the hair bundle on the apical surface of sensory hair cells in the cochlea, are responsible for mechanosensation and ultimately the perception of sound. The actin cytoskeleton of the stereocilia contains hundreds of tightly cross-linked parallel actin filaments in a paracrystalline array and it is vital for their function. Although several genes have been identified and associated with stereocilia development, the molecular mechanisms responsible for stereocilia growth, maintenance and organisation of the hair bundle have not been fully resolved. Here we provide further characterisation of the stereocilia of the whirler mouse mutant. We found that a lack of whirlin protein in whirler mutants results in short stereocilia with larger diameters without a corresponding increase in the number of actin filaments in inner hair cells. However, a decrease in the actin filament packing density was evident in the whirler mutant. The electron-density at the tip of each stereocilium was markedly patchy and irregular in the whirler mutants compared with a uniform band in controls. The outer hair cell stereocilia of the whirler homozygote also showed an increase in diameter and variable heights within bundles. The number of outer hair cell stereocilia was significantly reduced and the centre-to-centre spacing between the stereocilia was greater than in the wildtype. Our findings suggest that whirlin plays an important role in actin filament packing and dynamics during postnatal stereocilium elongation. Cell Motil. Cytoskeleton 2007.Keywords
This publication has 35 references indexed in Scilit:
- A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing lossHuman Genetics, 2006
- Auditory mechanotransduction in the absence of functional myosin‐XVaThe Journal of Physiology, 2006
- Whirlin complexes with p55 at the stereocilia tip during hair cell developmentProceedings of the National Academy of Sciences, 2006
- Development and properties of stereociliary link types in hair cells of the mouse cochleaJournal of Comparative Neurology, 2005
- Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereociliaNature Cell Biology, 2005
- Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directlyHuman Molecular Genetics, 2004
- Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereociliumHuman Molecular Genetics, 2004
- Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Nature Genetics, 2003
- Elongation of hair cell stereocilia is defective in the mouse mutant whirlerJournal of Comparative Neurology, 2002
- Actin filaments, stereocilia, and hair cells of the bird cochleaDevelopmental Biology, 1986