Literature DB >> 15537874

Organ of Corti potentials and the motion of the basilar membrane.

Anders Fridberger1, Jacques Boutet de Monvel, Jiefu Zheng, Ning Hu, Yuan Zou, Tianying Ren, Alfred Nuttall.   

Abstract

During sound stimulation, receptor potentials are generated within the sensory hair cells of the cochlea. Prevailing theory states that outer hair cells use the potential-sensitive motor protein prestin to convert receptor potentials into fast alterations of cellular length or stiffness that boost hearing sensitivity almost 1000-fold. However, receptor potentials are attenuated by the filter formed by the capacitance and resistance of the membrane of the cell. This attenuation would limit cellular motility at high stimulus frequencies, rendering the above scheme ineffective. Therefore, Dallos and Evans (1995a) proposed that extracellular potential changes within the organ of Corti could drive cellular motor proteins. These extracellular potentials are not filtered by the membrane. To test this theory, both electric potentials inside the organ of Corti and basilar membrane vibration were measured in response to acoustic stimulation. Vibrations were measured at sites very close to those interrogated by the recording electrode using laser interferometry. Close comparison of the measured electrical and mechanical tuning curves and time waveforms and their phase relationships revealed that those extracellular potentials indeed could drive outer hair cell motors. However, to achieve the sharp frequency tuning that characterizes the basilar membrane, additional mechanical processing must occur inside the organ of Corti.

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Year:  2004        PMID: 15537874      PMCID: PMC6730184          DOI: 10.1523/JNEUROSCI.2711-04.2004

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.709


  35 in total

1.  Somatic stiffness of cochlear outer hair cells is voltage-dependent.

Authors:  D Z He; P Dallos
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

2.  High-frequency electromotile responses in the cochlea.

Authors:  Karl Grosh; Jiefu Zheng; Yuan Zou; Egbert de Boer; Alfred L Nuttall
Journal:  J Acoust Soc Am       Date:  2004-05       Impact factor: 1.840

3.  Prestin is the motor protein of cochlear outer hair cells.

Authors:  J Zheng; W Shen; D Z He; K B Long; L D Madison; P Dallos
Journal:  Nature       Date:  2000-05-11       Impact factor: 49.962

4.  Electromotile hearing: evidence from basilar membrane motion and otoacoustic emissions.

Authors:  A L Nuttall; T Ren
Journal:  Hear Res       Date:  1995-12       Impact factor: 3.208

5.  Saturation of outer hair cell receptor currents causes two-tone suppression.

Authors:  C D Geisler; G K Yates; R B Patuzzi; B M Johnstone
Journal:  Hear Res       Date:  1990-03       Impact factor: 3.208

6.  Whole cell currents and mechanical responses of isolated outer hair cells.

Authors:  J Santos-Sacchi; J P Dilger
Journal:  Hear Res       Date:  1988-09-15       Impact factor: 3.208

7.  Transducing mechanisms in the lateral line canal organ receptors.

Authors:  A Flock
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1965

8.  Evoked mechanical responses of isolated cochlear outer hair cells.

Authors:  W E Brownell; C R Bader; D Bertrand; Y de Ribaupierre
Journal:  Science       Date:  1985-01-11       Impact factor: 47.728

9.  High-frequency motility of outer hair cells and the cochlear amplifier.

Authors:  P Dallos; B N Evans
Journal:  Science       Date:  1995-03-31       Impact factor: 47.728

10.  Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier.

Authors:  M Charles Liberman; Jiangang Gao; David Z Z He; Xudong Wu; Shuping Jia; Jian Zuo
Journal:  Nature       Date:  2002-08-28       Impact factor: 49.962

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  36 in total

1.  Outer hair cell somatic electromotility in vivo and power transfer to the organ of Corti.

Authors:  Sripriya Ramamoorthy; Alfred L Nuttall
Journal:  Biophys J       Date:  2012-02-07       Impact factor: 4.033

2.  Response to a pure tone in a nonlinear mechanical-electrical-acoustical model of the cochlea.

Authors:  Julien Meaud; Karl Grosh
Journal:  Biophys J       Date:  2012-03-20       Impact factor: 4.033

Review 3.  Electromechanical models of the outer hair cell composite membrane.

Authors:  A A Spector; N Deo; K Grosh; J T Ratnanather; R M Raphael
Journal:  J Membr Biol       Date:  2006-05-25       Impact factor: 1.843

4.  High-frequency force generation in the constrained cochlear outer hair cell: a model study.

Authors:  Zhijie Liao; Aleksander S Popel; William E Brownell; Alexander A Spector
Journal:  J Assoc Res Otolaryngol       Date:  2005-12

5.  Sound-evoked radial strain in the hearing organ.

Authors:  Igor Tomo; Jacques Boutet de Monvel; Anders Fridberger
Journal:  Biophys J       Date:  2007-06-29       Impact factor: 4.033

6.  Three-dimensional current flow in a large-scale model of the cochlea and the mechanism of amplification of sound.

Authors:  Pavel Mistrík; Chris Mullaley; Fabio Mammano; Jonathan Ashmore
Journal:  J R Soc Interface       Date:  2009-03-06       Impact factor: 4.118

7.  Non-uniform distribution of outer hair cell transmembrane potential induced by extracellular electric field.

Authors:  Sripriya Ramamoorthy; Teresa M Wilson; Tao Wu; Alfred L Nuttall
Journal:  Biophys J       Date:  2013-12-17       Impact factor: 4.033

8.  Detection of cochlear amplification and its activation.

Authors:  Wei Dong; Elizabeth S Olson
Journal:  Biophys J       Date:  2013-08-20       Impact factor: 4.033

Review 9.  Prestin and the cochlear amplifier.

Authors:  Peter Dallos; Jing Zheng; Mary Ann Cheatham
Journal:  J Physiol       Date:  2006-07-27       Impact factor: 5.182

10.  Coupling active hair bundle mechanics, fast adaptation, and somatic motility in a cochlear model.

Authors:  Julien Meaud; Karl Grosh
Journal:  Biophys J       Date:  2011-06-08       Impact factor: 4.033

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