Literature DB >> 1941076

Reversible inhibition of voltage-dependent outer hair cell motility and capacitance.

J Santos-Sacchi1.   

Abstract

Outer hair cells (OHC) from the organ of Corti are capable of fast voltage-induced length changes (Santos-Sacchi and Dilger, 1988), suggesting that an associated voltage sensor should reside in the OHC plasma membrane. Voltage-dependent mechanical responses and nonlinear charge movement of isolated OHCs from the guinea pig were analyzed using the whole-cell voltage-clamp technique. Ionic currents in the cells were blocked. Nonlinear voltage-dependent charge movement or, correspondingly, voltage-dependent capacitance was measured with step or AC analysis. OHC movements were measured either from video or using a differential photodiode technique. Maximum charge movements up to 2.5 pC were measured in OHCs from the low-frequency region of the cochlea. Both AC and step analyses indicated a peak nonlinear capacitance of 16-17 pF. The voltage dependence was fit to a Boltzmann relation with the step analysis indicating a maximum nonlinear capacitance at -23 mV step potential from a holding potential of about -120 mV, and AC analysis indicating a maximum at a holding potential near -40 mV. AC analysis probably provides a more accurate evaluation of voltage dependence. Measures of OHC motility magnitude versus voltage follow the nonlinear capacitance-voltage function obtained from AC measures. Treatment of the cells with gadolinium ions (0.5-1 mM) blocked OHC motility. This treatment also produced a shift of the nonlinear capacitance function along the voltage axis in the depolarizing direction, which can be explained by membrane surface charge screening. However, maximum capacitance was reduced as well and may correspond to the reduction or abolition of OHC motility in response to gadolinium treatment. Gadolinium effects were reversible. Nonlinear capacitance is not a function of membrane deformation due to length changes, since removal of OHC cytosol via the patch pipette abolished longitudinal movement but did not reduce nonlinear charge movement. It is interesting to note that the nonlinear capacitance will dynamically influence the time constant of the OHC during acoustically evoked receptor potential generation.

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Year:  1991        PMID: 1941076      PMCID: PMC6575435     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  185 in total

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2.  Effects of membrane potential and tension on prestin, the outer hair cell lateral membrane motor protein.

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Journal:  J Physiol       Date:  2001-03-15       Impact factor: 5.182

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Authors:  D Oliver; B Fakler
Journal:  J Physiol       Date:  1999-09-15       Impact factor: 5.182

5.  Electrically driven motor in the outer hair cell: effect of a mechanical constraint.

Authors:  M Adachi; K H Iwasa
Journal:  Proc Natl Acad Sci U S A       Date:  1999-06-22       Impact factor: 11.205

6.  A membrane bending model of outer hair cell electromotility.

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Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

7.  Fluctuation of motor charge in the lateral membrane of the cochlear outer hair cell.

Authors:  X Dong; D Ehrenstein; K H Iwasa
Journal:  Biophys J       Date:  2000-10       Impact factor: 4.033

8.  Piezoelectric reciprocal relationship of the membrane motor in the cochlear outer hair cell.

Authors:  Xiao-xia Dong; Mark Ospeck; Kuni H Iwasa
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

9.  A two-state piezoelectric model for outer hair cell motility.

Authors:  K H Iwasa
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

10.  Pivotal role of actin depolymerization in the regulation of cochlear outer hair cell motility.

Authors:  Nozomu Matsumoto; Rei Kitani; Anastasiya Maricle; Melissa Mueller; Federico Kalinec
Journal:  Biophys J       Date:  2010-10-06       Impact factor: 4.033

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