Journal
CELL CALCIUM
Volume 33, Issue 3, Pages 185-195Publisher
CHURCHILL LIVINGSTONE
DOI: 10.1016/S0143-4160(02)00228-2
Keywords
cochlear amplifier; prestin; olivocohlear bundle; acetylcholine; intracellular calcium stores; slow motility
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Two Ca2+-dependent mechanisms have been proposed to regulate the mechanical properties of outer hair cells (OHCs), the sensory-motor receptors of the mammalian cochlea. One involves the efferent neurotransmitter, acetylcholine, decreasing OHC axial stiffness. The other depends on elevation of intracellular free Ca2+ concentration ([Ca2+](i)) resulting in OHC elongation, a process known as Ca2+-dependent slow motility. Here we provide evidence that both these phenomena share a common mechanism. In whole-cell patch-clamp conditions, a fast increase of [Ca2+](i) by UV-photolysis of caged Ca2+ or by extracellular application of Ca2+-ionophore, ionomycin, produced relatively slow (time constant similar to20 s) cell elongation. When OHCs were partially collapsed by applying minimal negative pressure through the patch pipette, elevation of the [Ca2+](i) up to millimole levels (estimated by Fura-2) was unable to restore the cylindrical shape of the OHC. Stiffness measurements with vibrating elastic probes showed that the increase of [Ca2+], causes a decrease of OHC axial stiffness, with time course similar to that of the Ca2+-dependent elongation, without developing any measurable force. We concluded that, contrary to a previous proposal, Ca2+-induced OHC elongation is unlikely to be driven by circumferential contraction of the lateral wall, but is more likely a passive mechanical reaction of the turgid OHC to Ca2+-induced decrease of axial stiffness. This may be the key phenomenon for controlling gain and operating point of the cochlear amplifier. (C) 2003 Elsevier Science Ltd. All rights reserved.
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