Studies in Cochlear Hair Cell Transduction

Project: Research project

Description

DESCRIPTION In mammals, outer hair cells provide local amplification in the cochlea that is responsible for the ear's remarkable sensitivity and frequency selectivity. While the reliance of the mammalian cochlea on local, outer hair cell based-based amplification is widely accepted, there is no agreement about the amplifying mechanism. One view is that, powered by the cell's receptor potential, somatic shape changes, called electromotility, provide mechanical feedback and thereby amplification. An alternative concept is that amplification arises as an adjunct to the cell's forward transducer process and thus resides in the sterocilia. We have now identified the gene that codes for the specialized motor protein (prestin) that produces electromotility. Thus, it is now possible to test these alternatives. We shall produce a mouse-model that lacks prestin (knockout mouse) and test its hearing. Normal hearing will imply that the second mechanism of amplification is operative, whereas significant hearing loss will show that due to the non-functional prestin, hearing has been degraded. In addition, extensive experiments are conducted on the molecular properties of prestin itself with aims of producing various antibodies against it, to determine its topology and its interaction with various agents that are known to influence outer hair cell motility.
StatusFinished
Effective start/end date4/1/013/31/06

Funding

  • National Institute on Deafness and Other Communication Disorders (5 R01 DC000089-35)

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Outer Auditory Hair Cells
Auditory Hair Cells
Cochlea
Hearing
Hearing Tests
Transducers
Hearing Loss
Knockout Mice
Cell Movement
Ear
Mammals
Antibodies
Genes
Proteins