Hair Cell Bundles: Flexoelectric Motors of the Inner Ear
نویسندگان
چکیده
Microvilli (stereocilia) projecting from the apex of hair cells in the inner ear are actively motile structures that feed energy into the vibration of the inner ear and enhance sensitivity to sound. The biophysical mechanism underlying the hair bundle motor is unknown. In this study, we examined a membrane flexoelectric origin for active movements in stereocilia and conclude that it is likely to be an important contributor to mechanical power output by hair bundles. We formulated a realistic biophysical model of stereocilia incorporating stereocilia dimensions, the known flexoelectric coefficient of lipid membranes, mechanical compliance, and fluid drag. Electrical power enters the stereocilia through displacement sensitive ion channels and, due to the small diameter of stereocilia, is converted to useful mechanical power output by flexoelectricity. This motor augments molecular motors associated with the mechanosensitive apparatus itself that have been described previously. The model reveals stereocilia to be highly efficient and fast flexoelectric motors that capture the energy in the extracellular electro-chemical potential of the inner ear to generate mechanical power output. The power analysis provides an explanation for the correlation between stereocilia height and the tonotopic organization of hearing organs. Further, results suggest that flexoelectricity may be essential to the exquisite sensitivity and frequency selectivity of non-mammalian hearing organs at high auditory frequencies, and may contribute to the "cochlear amplifier" in mammals.
منابع مشابه
Actuation of flexoelectric membranes in viscoelastic fluids with applications to outer hair cells E . E . Herrera - Valencia
Liquid crystal flexoelectric actuation uses an imposed electric field to create membrane bending, and it is used by the outer hair cells (OHCs) located in the inner ear, whose role is to amplify sound through generation of mechanical power. Oscillations in the OHC membranes create periodic viscoelastic flows in the contacting fluid media. A key objective of this work on flexoelectric actuation ...
متن کاملActuation of Flexoelectric Membranes in Viscoelastic Fluids with Application to Outer Hair Cells
Liquid crystal flexoelectric actuation uses an imposed electric field to create membrane bending and it is used by the Outer Hair Cells (OHC) located in the inner ear, whose role is to amplify sound through generation of mechanical power. Oscillations in the OHC membranes create periodic viscoelastic flows in the contacting fluid media. A key objective of this work on flexoelectric actuation re...
متن کاملActuation of flexoelectric membranes in viscoelastic fluids with applications to outer hair cells.
Liquid crystal flexoelectric actuation uses an imposed electric field to create membrane bending, and it is used by the outer hair cells (OHCs) located in the inner ear, whose role is to amplify sound through generation of mechanical power. Oscillations in the OHC membranes create periodic viscoelastic flows in the contacting fluid media. A key objective of this work on flexoelectric actuation ...
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Auditory and vestibular functions in vertebrates depend on the transduction of sound vibration or head acceleration into electrical responses in inner ear hair cells. Mechanoelectrical transduction occurs at the tip of stereocilia, which are polarized to form an orientational arrangement that determines directional sensitivity. It remains to be clarified when and how premature hair cells acquir...
متن کاملShaky hearing
Functional sensory hair cells in the inner ear have specialised microvilli — stereocilia — which are essential for hearing. The scanning electron micrograph at top shows the normal arrangement of stereocilia bundles on three outer hair cells in the inner ear of a three-day-old mouse. The stereocilia grow to form rows of graded height in a distinctive V-shaped bundle. Recent studies in mice have...
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عنوان ژورنال:
- PLoS ONE
دوره 4 شماره
صفحات -
تاریخ انتشار 2009