The outer hair cell is a critical factor for fine tuning and for the wide dynamic range of the mammalian ear. We have demonstrated earlier that this cell has an unusual membrane motor which directly uses electrical energy available at the plasma membrane. Charges transferable across the membrane enable the motor to obtain electrical energy, and coupling between charge transfers and changes in the membrane area enables conversion into mechanical energy. Such charge transfers are observed as an excess membrane capacitance. A direct energy conversion mechanism requires that the membrane capacitance be dependent on both the membrane potential and membrane tension. That indeed is the case. We are studying electrical and mechanical properties of the outer hair cell to clarify details of this novel motile mechanism. We recently found that turgor pressure of the cell does not affect the amplitude of the voltage-dependent motility. This observation indicates that the motile mechanism is indeed based on membrane area changes as we had assumed earlier. Deformations of the cell can be explained by membrane elasticity for the time scale that corresponds to the auditory frequencies. We have been trying to incorporate the motor and the mechanical characteristics of the outer hair cell into theoretical models. Our updated model predicts force generation of 0.1 nN/mV for a single cell, agreeing with our experiment. Although we recently found that the basal part of the cell is softer than the rest of the cell, we found that such inhomogeneity does not affect our earlier force and stiffness measurements. In addition to the unique energy source, the high speed of the response, which apparently exceeds 10 kHz, characterizes this motility. We recently formulated a theory predicting that the intrinsic speed of the membrane motor can be determined by the frequency dependence of the membrane capacitance and spectral strength of membrane noise due to flipping of motor charges. We are currently examining these features experimentally. These efforts are aimed at further clarification of the mechanism of outer hair cell motility and its biological role.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Intramural Research (Z01)
Project #
1Z01DC000010-07
Application #
6104216
Study Section
Special Emphasis Panel (LCB)
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
1998
Total Cost
Indirect Cost
Name
National Institute on Deafness and Other Communication Disorders
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Sul, Bora; Iwasa, Kuni H (2009) Amplifying effect of a release mechanism for fast adaptation in the hair bundle. J Acoust Soc Am 126:4-6
Fang, Jie; Iwasa, K H (2007) Effects of chlorpromazine and trinitrophenol on the membrane motor of outer hair cells. Biophys J 93:1809-17
Fang, Jie; Iwasa, K H (2006) Effects of tarantula toxin GsMTx4 on the membrane motor of outer hair cells. Neurosci Lett 404:213-6
Ospeck, Mark; Dong, Xiao-Xia; Fang, Jie et al. (2006) Electromotility in outer hair cells: a supporting role for fast potassium conductance. ORL J Otorhinolaryngol Relat Spec 68:373-7
Dong, X-X; Iwasa, K H (2004) Tension sensitivity of prestin: comparison with the membrane motor in outer hair cells. Biophys J 86:1201-8
Ospeck, Mark; Dong, Xiao-xia; Iwasa, Kuni H (2003) Limiting frequency of the cochlear amplifier based on electromotility of outer hair cells. Biophys J 84:739-49
Iwasa, K H; Ehrenstein, G (2002) Cooperative interaction as the physical basis of the negative stiffness in hair cell stereocilia. J Acoust Soc Am 111:2208-12
Dong, Xiao-xia; Ospeck, Mark; Iwasa, Kuni H (2002) Piezoelectric reciprocal relationship of the membrane motor in the cochlear outer hair cell. Biophys J 82:1254-9
Iwasa, K H (2001) A two-state piezoelectric model for outer hair cell motility. Biophys J 81:2495-506
Kakehata, S; Dallos, P; Brownell, W E et al. (2000) Current concept of outer hair cell motility. Auris Nasus Larynx 27:349-55

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