Abstract
This chapter is centered on the proposal that evolutionary changes in prestin provide the basis for the amplifying, impedance-matching, molecular link that harnesses the outer hair cells (OHCs) of the mammalian cochlea, via specialized supporting cells of the organ of Corti, to the enormous frequency range of the mechanically tuned basilar membrane. This devolution of frequency tuning from potential, intrinsic, frequency-tuning, mechanisms of the OHCs, themselves to an extrinsic source of frequency tuning has enabled mammals to listen to sounds over an enormous range of frequencies from infrasound to frequencies way beyond the auditory ranges of other amniotes. The final section of the chapter is concerned with the evidence that forces generated by prestin are under direct, inhibitory, centrifugal efferent neural control from the central nervous system.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Albert, J. T., Winter, H., Schaechinger, T. J., Weber, T., Wang, X., He, D. Z. Z., Hendrich, O., Geisler, H-S., Zimmermann, U., Oelmann, K., Knipper, M., Göpfert, M. C., & Oliver, D. (2007). Voltage-sensitive prestin orthologue expressed in zebrafish hair cells. Journal of Physiology, 580, 451–461.
Angelborg, C., & Engstrom, H. (1973). The normal organ of Corti. In A. R. Moller (Ed.), Basic mechanisms of hearing (pp. 125–182). New York and London: Academic Press.
Arnold, W., & Anniko, M. (1989). Supporting and membrane structures of human outer hair cells: Evidence for an isometric contraction. Oto-Rhino-Laryngology, 51, 339–353.
Ashmore, J. (2008). Cochlear outer hair cell motility. Physiological Reviews, 88, 173–210.
Beurg, M., Tan, X. & Fettiplace, R. (2013). A prestin motor in chicken auditory hair cells: active force generation in a nonmammalian species. Neuron, 79, 69–81.
Bezanilla, F. (2008). How membrane proteins sense voltage. Nature Revues in Molecular and Cellular Biology, 9, 323–332.
Blanchet, C., Erostegui, C., Sugasawa, M., & Dulon, D. (1996). Acetylcholine-induced potassium current of guinea pig outer hair cells: Its dependence on a calcium influx through nicotinic-like receptors. Journal of Neuroscience, 16, 2574–2584.
Bobbin, R. P. (2001). ATP-induced movement of the stalks of isolated cochlear Deiters’ cells. NeuroReport, 12, 2923–2926.
Bobbin, R. P., Campbell, J., Lousteau, S., & Mandhare, M. (2002). Electrical and ATP induced movements of the phalangeal processes of isolated cochlear Deiters’ cells. In C. I. Berlin, L. J. Hood, & A. Ricci (Eds.), Hair cell micromechanics and otoacoustic emissions (pp. 91–106). Clifton Park, NY: Thomson Delmar Learning.
Brownell, W. E., Bader, C. R., Bertrand, D., & De, R.Y. (1985). Evoked mechanical responses of isolated cochlear outer hair cells. Science, 227, 194–196.
Bruns, V., & Schmieszek, E. (1980). Cochlear innervation in the greater horseshoe bat: Demonstration of an acoustic fovea. Hearing Research, 3, 27–43.
Bruns, V., Müller, M., Hofer, W., Heth, G. & Nevo, E. (1988). Inner ear structure and electrophysiological audiograms of the subterranean mole rat, Spalax ehrenbergi. Hearing Research, 33(1), 1–9.
Cazals, Y., Aran, J. M., Erre, J. P., Guilhaume, A., & Aurousseau, C. (1983) Vestibular acoustic reception in the guinea pig: A saccular function? Acta Oto-Laryngologica, 95(3–4), 211–217.
Chen, F., Zha, D., Fridberger, A., Zheng, J., Choudhury, N., Jacques, S. L., Wang, R. K., Shi, X., & Nuttall, A. L. (2011). A differentially amplified motion in the ear for near-threshold sound detection. Nature Neuroscience, 14, 770–774.
Cooper, N. P., & Guinan, J. J. (2003). Separate mechanical processes underlie fast and slow effects of medial olivocochlear efferent activity. Journal of Physiology (London), 548, 307–312.
Cooper, N. P., & Guinan, J. J. Jr. (2006). Efferent-mediated control of basilar membrane motion. Journal of Physiology, 576, 49–54.
Dallos, P., & Fakler, B. (2002). Prestin, a new type of motor protein. Nature Revues in Molecular and Cellular Biology, 3, 104–111.
Dallos, P., He, D. Z., Lin, X., Sziklai, I., Mehta, S., & Evans, B. N. (1997). Acetylcholine, outer hair cell electromotility, and the cochlear amplifier. Journal of Neuroscience, 17, 2212–2226.
Dallos, P., Wu, X., Cheatham, M. A., Gao, J., Zheng, J., Anderson, C. T., Jia, S., Wang, X., Cheng, W. H., Sengupta, S., He, D. Z., & Zuo, J. (2008). Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron, 58, 333–339.
Dannhof, B. J., & Bruns, V. (1991). The organ of Corti in the bat Hipposideros bicolor. Hearing Research, 53, 253–268.
Davis, H. (1982). An active process in cochlear mechanics. Hearing Research, 9, 79–90.
Deak, L., Zheng, J, Orem, A., Du, G. G., Aguinaga, S., Matsuda, K., & Dallos, P. (2005). Effects of cyclic nucleoticles on the function of prestin. Journal of Physiology (London), 563, 483–496.
Didier, A., & Cazals, Y. (1989). Acoustic responses recorded from the saccular bundle on the eighth nerve of the guinea pig. Hearing Research, 37(2),123–127.
Dulon, D., Zajic, G., & Schacht, J. (1990). Increasing intracellular free calcium induces circumferential contractions in isolated cochlear outer hair-cells. Journal of Neuroscience, 10, 1388–1397.
Dulon, D., Blanchet, C., & Laffon, E. (1994). Photo-released intracellular Ca2+ evokes reversible mechanical responses in supporting cells of the guinea-pig organ of Corti. Biochemical Biophysical Research Communications, 201, 1263–1269.
Elgoyhen, A. B., & Franchini, L. F. (2011). Prestin and the cholinergic receptor of hair cells: Positively-selected proteins in mammals. Hearing Research, 273, 100–108.
Elgoyhen, A. B., & Katz, E. (2012). The efferent medial olivocochlear-hair cell synapse. Journal of Physiology Paris, 106(1–2):47–56.
Evans, M. G. (1996). Acetylcholine activates two currents in guinea-pig outer hair cells. Journal of Physiology, 491, 563–578.
Fang, J., Izumi, C., & Iwasa, K. H. (2010). Sensitivity of prestin-based membrane motor to membrane thickness. Biophysical Journal, 98, 2831–2838.
Fay, R. R., (1988). Hearing in Vertebrates: a Psychophysics Databook. Hill-Fay Associates, Winnetka, IL.
Fettiplace, R., & Hackney, C. M. (2006). The sensory and motor roles of auditory hair cells. Nature Revue of Neuroscience, 7, 19–29.
Fex, J. (1967). Efferent inhibition in the cochlea related to hair-cell dc activity: Study of postsynaptic activity of the crossed olivocochlear fibres in the cat. Journal of the Acoustical Society of America, 41, 666–675.
Flock, A., Flock, B., Fridberger, A., Scarfone, E., & Ulfendahl, M. (1999). Supporting cells contribute to control of hearing sensitivity. Journal of Neuroscience, 19, 4498–4507.
Franchini, L. F., & Elgoyhen, A. B. (2006). Adaptive evolution in mammalian proteins involved in cochlear outer hair cell electromotility. Molecular Phylogenetics and Evolution, 41, 622–635.
Frank, G., Hemmert, W., & Gummer, A. W. (1999). Limiting dynamics of high frequency electromechanical transduction of outer hair cells. Proceedings of the National Academy of Sciences of the USA, 96, 4420–4425.
Fridberger, A., Flock, A., Ulfendahl, M., & Flock, B. (1999). Acoustic overstimulation increases outer hair cell Ca2+ concentrations and causes dynamic contractions of the hearing organ. Proceedings of the National Academy of Sciences of the USA, 95, 7127–7132.
Fridberger, A., Tomo, I., Ulfendahl, M., & Boutet de Monvel, J. (2006). Imaging hair cell transduction at the speed of sound: Dynamic behavior of mammalian stereocilia. Proceedings of the National Academy of Sciences of the USA, 103, 1918–1923.
Frolenkov, G. I., Mammano, F., Belyantseva, I. A., Coling, D., & Kachar, B. (2000). Two distinct Ca2+-dependent signaling pathways regulate the motor output of cochlear outer hair cells. Journal of Neuroscience, 20, 5940–5948.
Frolenkov, G. I., Mammano, F., & Kachar, B. (2003). Regulation of outer hair cell cytoskeletal stiffness by intracellular Ca2+: Underlying mechanism and implications for cochlear mechanics. Cell Calcium, 33, 85–195.
Fuchs, P. A. (1992). Ionic currents in cochlear hair cells. Progress in Neurobiology, 39, 493–505.
Gao, J., Wang, X., Wu, X., Aguinaga, S., Huynh, K., Jia, S., Matsuda, K., Patel, M., Zheng, J., Cheatham, M., He, D. Z., Dallos, P., & Zuo, J. (2007). Prestin-based outer hair cell electromotility in knockin mice does not appear to adjust the operating point of a cilia-based amplifier. Proceedings of the National Academy of Sciences of the USA, 104, 12542–12547.
Gavara, N., Manoussaki, D., & Chadwick, R. S. (2011). Auditory mechanics of the tectorial membrane and the cochlear spiral. Current Opinion in Otolaryngology & Head and Neck Surgery, 19, 382–387.
Geisler, C. D., & Sang, C. (1995). A cochlear model using feed-forward outer-hair-cell forces. Hearing Research, 86, 132–146.
Guinan, J. J. (1996). Physiology of olivocochlear efferents. In P. Dallos, A. N. Popper, & R. R. Fay (Eds.), The cochlea (pp. 435–502). New York: Springer-Verlag.
Gummer, A. W., Smolders, J. W., & Klinke, R. (1987). Basilar membrane motion in the pigeon measured with the Mössbauer technique. Hearing Research, 29, 63–92.
Hallworth, R. (1995). Passive compliance and active force generation in the guinea pig outer hair cell. Journal of Neurophysiology, 74, 2319–2328.
He, D. Z., & Dallos, P. (1999). Somatic stiffness of cochlear outer hair cells is voltage dependent. Proceedings of the National Academy of Sciences of the USA, 96, 8223–8228.
He, D. Z., Jia, S., & Dallos, P. (2003a). Prestin and the dynamic stiffness of cochlear outer hair cells. Journal of Neuroscience, 23, 9089–9096.
He, D. Z., Beisel, K. W., Chen, L., Ding, D. L., Jia, S., Fritzsch, B., & Salvi, R. (2003b). Chick hair cells do not exhibit voltage-dependent somatic motility. Journal of Physiology, 546, 511–520.
Heffner, R. S. (2004). Primate hearing from a mammalian perspective. Anatomical Record, 281A, 1111–1122.
Heffner, R. S., & Heffner, H. E., (1982). Hearing in the elephant: absolute thresholds, frequency discrimination, and sound localization. Journal of Comparative Physiology and Psychology, 96, 926–944.
Heffner, R. S., & Heffner, H. E. (1992). Hearing and sound localization in blind mole rats (Spalax ehrenbergi). Hearing Research, 62, 206–216.
Heffner, R. S., & Heffner, H. E. (1993). Degenerate hearing and sound localization in naked mole rats (Heterocephalus glaber), with an overview of central auditory structures. Journal of Comparative Neurology, 331, 418–433.
Henson, M. M., & Henson, O. W., Jr. (1979). Some aspects of the structural organization in the cochlea of the bat, Pteronotus parnellii. Scanning Electron Microscopy, 111, 975–979.
Henson, M. M., & Henson, O. W., Jr. (1988). Tension fibroblasts and the connective tissue matrix of the spiral ligament. Hearing Research, 35(2–3), 237–258.
Heth, G., Frankenberg, E., & Nevo, E. (1986). Adaptive optimal sound for vocal communication in tunnels of a subterranean mammal (Spalax ehrenbergi). Experientia, 42, 1287–1289.
Heth, G., Frankenberg, E., & Nevo, E. (1988). “Courtship” call of subterranean mole rats (Spalax ehrenbergi): Physical analysis. Journal of Mammalogy, 69, 121–125.
Housley, G. D., & Ashmore, J. F. (1991). Direct measurement of the action of acetylcholine on isolated outer hair cells of the guinea pig cochlea. Proceedings of the Royal Society of London B: Biological Sciences, 244, 161–167.
Iwasa, K. H. (1993). Effect of stress on the membrane capacitance of the auditory outer hair cell. Biophysical Journal, 65, 492–498.
Iwasa, K. H., & Adachi, M. (1997). Force generation in the outer hair cell of the cochlea. Biophysical Journal, 73(1), 546–555.
Izumi, C., Bird, J. E., & Iwasa, K. H. (2011). Membrane thickness sensitivity of prestin orthologs: The evolution of a piezoelectric protein. Biophysical Journal, 100, 2614–2622.
Jacob, S., Pienkowski, M., & Fridberger, A. (2011). The endocochlear potential alters cochlear micromechanics. Biophysical Journal, 100, 2586–2594.
Johnson, S. L., Beurg, M., Marcotti, W., & Fettiplace, R. (2011). Prestin-driven cochlear amplification is not limited by the outer hair cell membrane time constant. Neuron, 70(6), 1143–1154.
Jones, G. P., Lukashkina, V. A., Russell, I. J., Lukashkin, A. N. (2010). The vestibular system mediates sensation of low-frequency sounds in mice. Journal of the Association of Research in Otolaryngology, 11(4), 725–732.
Kakehata, S., & Santos-Sacchi, J. (1995). Membrane tension directly shifts voltage dependence of outer hair cell motility and associated gating charge. Biophysical Journal, 68, 2190–2197.
Köppl, C. (2011). Birds–—same thing, but different? Convergent evolution in the avian and mammalian auditory systems provides informative comparative models. Hearing Research, 273, 65–71.
Köppl, C., Forge, A., & Manley, G. A. (2004). Low density of membrane particles in auditory hair cells of lizards and birds suggests an absence of somatic motility. Journal of Comparative Neurology, 479, 149–155.
Kössl, M., & Russell, I. J. (1995). Basilar membrane resonance in the cochlea of the mustached bat. Proceedings of the National Academy of Sciences of the USA, 92, 276–279.
Lange, S., Burda, H., Wegner, R. E., Dammann, P., Begall, S., & Kawalika, M. (2007). Living in a “stethoscope”: Burrow-acoustics promote auditory specializations in subterranean rodents. Naturwissenschaften, 94, 134–138.
Legan, P. K., Lukashkina, V. A., Goodyear, R. J., Kössl, M., Russell, I. J., & Richardson, G. P. (2000). A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback. Neuron, 28, 273–285.
Leves, F. P., Tierney, M. L., & Howitt, S. M. (2008). Polar residues in a conserved motif spanning helices 1 and 2 are functionally important in the SulP transporter family. International Journal of Biochemical Cell Biology, 40, 2596–2605.
Li, G., Wang, J. H., Rossiter, S. J., Jones, G., Cotton, J. A., & Zhang, S. Y. (2008). The hearing gene Prestin reunites echolocating bats. Proceedings of the National Academy of Sciences of the USA, 105, 13959–13964.
Li, Y., Liu, Z., Shi, P., & Zhang, J. Z. (2010). The hearing gene Prestin unites echolocating bats and whales. Current Biology, 20, R55–56.
Lim, D. J. (1986). Functional structure of the organ of Corti: A review. Hearing Research, 22, 117–146.
Liu, Y., Cotton, J. A., Shen, B., Han, X. Q., Rossiter, S. J., & Zhang, S. Y. (2010a). Convergent sequence evolution between echolocating bats and dolphins. Current Biology, 20, R53–54.
Liu, Y., Rossiter, S. J., Han, X. Q., Cotton, J. A., & Zhang, S. Y. (2010b). Cetaceans on a molecular fast track to ultrasonic hearing. Current Biology, 20, 1834–1839.
Long, G., & Schnitzler, H. U., (1975). Behavioral audiograms from the bat Rhinolophus ferrumequinum. Journal of Comparative Physiology A 100, 211–220.
Lukashkin, A. N., Walling, M. N., & Russell, I. J. (2007). Power amplification in the mammalian cochlea. Current Biology, 17, 1340–1344.
Lukashkin, A. N., Richardson, G. P., & Russell, I. J. (2010). Multiple roles for the tectorial membrane in the active cochlea. Hearing Research, 266, 26–35.
Mahendrasingam , S., Beurg, M., Fettiplace, R., & Hackney, C. M. (2010). The ultrastructural distribution of prestin in outer hair cells: A post-embedding immunogold investigation of low and high frequency regions of the rat cochlea. European Journal of Neuroscience, 31(9), 1595–1605.
Manley, G. A. (2000). Cochlear mechanisms from a phylogenetic viewpoint. Proceedings of the National Academy of Sciences of the USA, 97(22), 11736–11743.
Manley, G. (2011). Lizard auditory papillae: An evolutionary kaleidoscope. Hearing Research, 273, 59–64.
Manley, G. A., & Jones, T. A. (2011). The development and evolution of a tonotopic organization in the cochlea. Hearing Research, 273, 1–6.
Markin, V. S., & Hudspeth, A. J. (1995). Modeling the active process of the cochlea: phase relations, amplification, and spontaneous oscillation. Biophysical Journal, 69, 138–147.
Matsumoto, N., Kitani, R., Maricle, A., Mueller, M., & Kalinec, F. (2010). Pivotal role of actin depolymerization in the regulation of cochlear outer hair cell motility. Biophysical Journal, 99, 2067–2076.
Mellado Lagarde, M. M., Drexl, M., Lukashkin, A. N., Zuo, J., & Russell, I. J. (2008). A role for prestin in the frequency tuning of cochlear mechanical responses and their transmission to neural excitation. Current Biology, 18, 200–202.
McCue, M. P. & Guinan, J. J. Jr. (1994). Acoustically responsive fibers in the vestibular nerve of the cat. Journal of Neuroscience, 14, 6058–6070.
McCue, M. P., & Guinan, J. J. Jr. (1995). Spontaneous activity and frequency selectivity of acoustically responsive vestibular afferents in the cat. Journal of Neurophysiology, 74, 1563–1572.
Mountain, D. C., Hubbard, A. E., & McMullen, T. A. (1983). Electromechanical processes in the cochlea. In E. de Boer & M. A. Viergever (Eds.), Mechanics of Hearing (pp. 119–126). Delft, The Netherlands: Delft University Press.
Murugasu, E., & Russell, I. J. (1996a). The effect of efferent stimulation on basilar membrane displacement in the basal turn of the guinea pig cochlea. Journal of Neuroscience, 16, 325–332.
Murugasu, E., & Russell, I. J. (1996b). The role of calcium on the effects of intracochlear acetylcholine perfusion on basilar membrane displacement in the basal turn of the guinea pig cochlea. Auditory Neuroscience, 2, 363–376.
Neely, S. T., & Kim, D. O. (1983). An active cochlear model showing sharp tuning and high sensitivity. Hearing Research, 9, 123–l 30.
Neuweiler, G. (2000). The biology of bats. New York: Oxford University Press.
Nilsen, K. E., & Russell, I. J. (1999). Timing of cochlear feedback: Spatial and temporal representation of a tone across the basilar membrane. Nature Neuroscience, 2, 642–648.
Nilsen, N., Brownell, W. E., Sun, S. X., & Spector, A. A. (2011). Effect of membrane mechanics on charge transfer by the membrane protein prestin. Biomechanical Models of Mechanobiology, DOI 10.1007/s10237-011-0296-0.
Nowotny, M., & Gummer, A. W. (2006). Nanomechanics of the subtectorial space caused by electromechanics of cochlear outer hair cells. Proceedings of the National Academy of Sciences of the USA, 103, 2120–2125.
Nowotny, M., & Gummer, A. W. (2011). Vibration responses of the organ of Corti and the tectorial membrane to electrical stimulation. Journal of the Acoustical Society of America, 130, 3852–3872.
Okoruwa, O. E., Weston, M. D., Sanjeevi, D. C., Millemon, A. R., Fritzsch, B., Hallworth, R., & Beisel, K. W. (2008). Evolutionary insights into the unique electromotility motor of mammalian outer hair cells. Evolution and Development, 10, 300–315.
Oliver, D., Klocker, N., Schuck, J., Baukrowitz, T., Ruppersberg, J. P., & Fakler, B. (2000). Gating of Ca2+-activated K+ channels controls fast inhibitory synaptic transmission at auditory outer hair cells. Neuron, 26, 595–601.
Oliver, D., He, D. Z., Klocker, N., Ludwig, J., Schulte, U., Waldegger, S., Ruppersberg, J. P., Dallos, P., & Fakler, B. (2001). Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein. Science, 292, 2340–2343.
Rabbitt, R. D., Clifford, S., Breneman, K. D., Farrell, B., & Brownell, W. E. (2009). Power efficiency of outer hair cell somatic electromotility. PLoS Computational Biology, 5, e1000444.
Raphael, Y., & Altschuler, R. A. (2003). Structure and innervation of the cochlea. Brain Research Bulletin, 60, 397–422.
Raphael, Y., Lenoir, M., Wroblewski, R., & Pujol, R. (1991). The sensory epithelium and its innervation in the mole rat cochlea. Journal of Comparative Neurology, 314, 367–382.
Richardson, G. P., Lukashkin, A. N., & Russell, I. J. (2008). The tectorial membrane: One slice of a complex cochlear sandwich. Current Opinion in Otolaryngology & Head and Neck Surgery, 16, 458–464.
Robles, L., & Ruggero, M. A. (2001). Mechanics of the mammalian cochlea. Physiological Reviews, 81, 1305–1352.
Rossiter, S. J., Zhang, S., & Liu, Y. (2011). Prestin and high frequency hearing in mammals. Communicative & Integrative Biology, 4, 236–239.
Russell, I. J., & Kössl, M. (1991). The voltage responses of hair cells in the basal turn of the guinea-pig cochlea. Journal of Physiology, 435, 493–511.
Russell, I. J., & Kössl, M. (1992). Sensory transduction and frequency-selectivity in the basal turn of the guinea-pig cochlea. Philosophical Transactions of the Royal Society of London B: Biological Sciences, 336, 317–324.
Russell, I. J., & Kössl, M. (1999). Micromechanical responses to tones in the auditory fovea of the greater mustached bat’s cochlea. Journal of Neurophysiology, 82, 676–686.
Russell, I. J., & Lukashkin, A. N. (2008). Cellular and molecular mechanisms in the efferent control of cochlear nonlinearities. In G. A. Manley, R. R. Fay, & A. N. Popper (Eds.), Active processes and otoacoustic emissions in hearing (pp. 343–379). New York: Springer.
Russell, I. J., & Nilsen, K. E. (2000). The spatial and temporal representation of a tone on the guinea pig basilar membrane. Proceedings of the National Academy of Sciences of the USA, 97, 11751–11758.
Rybalchenko, V., & Santos-Sacchi, J. (2008). Anion control of voltage sensing by the motor protein prestin in outer hair cells. Biophysical Journal, 95, 4439–4447.
Santos-Sacchi, J. (1991). Reversible inhibition of voltage-dependent outer hair cell motility and capacitance. Journal of Neuroscience, 11, 3096–3110.
Santos-Sacchi, J. (1992). On the frequency limit and phase of outer hair cell motility: Effects of the membrane filter. Journal of Neuroscience, 12, 1906–1916.
Santos-Sacchi, J. (2008). Cochlear mechanics: No shout but a twist in the absence of prestin. Current Biology, 18, R304–306.
Santos-Sacchi, J., Kakehata, S., & Takahashi, S. (1998a). Effects of membrane potential on the voltage dependence of motility-related charge in outer hair cells of the guinea-pig. Journal of Physiology, 510, 225–235.
Santos-Sacchi, J., Kakehata, S., Kikuchi, T., Katori, Y., & Takasaka, T. (1998b). Density of motility-related charge in the outer hair cell of the guinea pig is inversely related to best frequency. Neuroscience Letters, 256, 155–158.
Santos-Sacchi, J., Song, L., Zheng, J., & Nuttall, A. L. (2006). Control of mammalian cochlear amplification by chloride anions. Journal of Neuroscience, 26, 3992–3998.
Schaechinger, T. J., & Oliver, D. (2007). Nonmammalian orthologs of prestin (SLC26A5) are electrogenic divalent/chloride anion exchangers. Proceedings of the National Academy of Sciences of the USA, 104, 7693–7698.
Schaechinger, T. J., Gorbunov, D., Halaszovich, C. R., Moser, T., Kügler, S., Fakler, B., & Oliver, D. (2011). A synthetic prestin reveals protein domains and molecular operation of outer hair cell piezoelectricity. EMBO Journal, 30, 2793–2804.
Shen, B., Avila-Flores, R., Liu, Y., Rossiter, S. J., & Zhang, S. (2011). Prestin shows divergent evolution between constant frequency echolocating bats. Journal of Molecular Evolution, 73, 109–115.
Slepecky, N. B. (1996). Structure of the mammalian cochlea. In P. Dallos, A. N. Popper, R. R. Fay (Eds.), The cochlea (pp. 44–129). New York: Springer.
Sridhar, T. S., Brown, M. C., & Sewell, W. F. (1997). Unique postsynaptic signaling at the hair cell efferent synapse permits calcium to evoke changes on two time scales. Journal of Neuroscience, 17, 428–437.
Tan, X., Pecka, J. L., Tang, J., Okoruwa, O. E., Zhang, Q., Beisel, K. W., & He, D. Z. (2011). From zebrafish to mammal: Functional evolution of prestin, the motor protein of cochlear outer hair cells. Journal of Neurophysiology, 105, 36–44.
Vater, M., & Kössl, M. (1996). Further studies on the mechanics of the cochlear partition in the mustached bat. I. Ultrastructural observations on the tectorial membrane and its attachments. Hearing Research, 94, 63–78.
Vater, M., & Kössl, M. (2011). Comparative aspects of cochlear functional organization in mammals. Hearing Research, 273, 89–99.
Vater, M., & Lenoir, M. (1992). Ultrastructure of the horseshoe bat’s organ of Corti. I. Scanning electron microscopy. Journal of Comparative Neurology, 31, 83367–83379.
Vater, M. Lenoir, M., & Pujol, R. (1992). Ultrastructure of the horseshoe bat’s organ of Corti. 11. Transmission electron microscopy. The Journal of Comparative Neurology, 31, 8380–8391.
Weddell, T., Mellado Lagarde, M. M., Lukashkina, V. A., Lukashkin, A. N., Zuo, J., & Russell, I. J. (2011). Prestin links extrinsic tuning to neural excitation in the mammalian cochlea. Current Biology, 21(18), R682–683.
Xiao, Z., & Suga, N. (2002). Modulation of cochlear hair cells by the auditory cortex in the mustached bat. Nature Neuroscience, 5, 57–63.
Yoon, Y. J., Steele, C. R., & Puria, S. (2011). Feed-forward and feed-backward amplification model from cochlear cytoarchitecture: An interspecies comparison. Biophysical Journal, 100, 1–10.
Young, E. D., Fernández, C., & Goldberg, J. M. (1977). Responses of squirrel monkey vestibular neurons to audio-frequency sound and head vibration. Acta Otolaryngologica, 84, 352–360.
Yu, N., & Zhao, H. B. (2009). Modulation of outer hair cell electromotility by cochlear supporting cells and gap junctions. PLoS One, 4, e7923.
Zheng, J., Shen, W., He, D. Z., Long, K. B., Madison, L. D., & Dallos, P. (2000). Prestin is the motor protein of cochlear outer hair cells. Nature, 405, 149–155.
Acknowledgments
I thank my research collaborators, Andrei Lukashkin, Victoria, Lukashkina, Marcia Mellado, Thomas Weddell, and Jian Zou for stimulating discussion and George Burwood, Gareth Jones, and Thomas Weddell for comments on the manuscript. Research was supported by the Medical Research Council.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer Science+Business Media New York
About this chapter
Cite this chapter
Russell, I. (2013). Roles for Prestin in Harnessing the Basilar Membrane to the Organ of Corti. In: Köppl, C., Manley, G., Popper, A., Fay, R. (eds) Insights from Comparative Hearing Research. Springer Handbook of Auditory Research, vol 49. Springer, New York, NY. https://doi.org/10.1007/2506_2013_23
Download citation
DOI: https://doi.org/10.1007/2506_2013_23
Published:
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4614-9076-0
Online ISBN: 978-1-4614-9077-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)