Activation and adaptation of transducer currents in turtle hair cells.

1. Transducer currents were recorded in turtle cochlear hair cells during mechanical stimulation of the hair bundle. The currents were measured under whole‐cell voltage clamp in isolated cells that were firmly stuck to the floor of the recording chamber. 2. Stimuli were calibrated by projecting the image of the hair bundle onto a rapidly scanned 128 photodiode array. This technique showed that, while the cell body was immobilized, the tip of the bundle would follow faithfully the motion of an attached glass probe up to frequencies of more than 1 kHz. 3. The relationship between inward transducer current and bundle displacement was sigmoidal. Maximum currents of 200‐400 pA were observed for deflections of the tip of the bundle of 0.5 microns, equivalent to rotating the bundle by about 5 deg. 4. In response to a step deflection of the bundle, the current developed with a time constant (about 0.4 ms for small stimuli) that decreased with the size of displacement. This suggests that the onset of the current was limited by the gating kinetics of the transduction channel. The onset time course was slowed about fourfold for a 20 degrees C drop in temperature. 5. For small maintained displacements, the current relaxed to about a quarter of the peak level with a time constant of 3‐5 ms. This adaptation was associated with a shift of the current‐displacement relationship in the direction of the stimulus. The rate and extent of adaptation were decreased by lowering external Ca2+. 6. Adaptation was strongly voltage sensitive, and was abolished at holding potentials positive to the reversal potential of the transducer current of about 0 mV. It was also diminished by loading cells with 10 mM of the Ca2+ chelator BAPTA. These observations suggest that adaptation may be partly controlled by influx of Ca2+ through the transducer channels. 7. Removal of adaptation produced asymmetric responses, with fast onsets but slow decays following return of the bundle to its resting position; the offset time course depended on both the magnitude and duration of the prior displacement. 8. In some experiments, hair bundles were deflected with a flexible glass fibre whose motion was monitored using a dual photodiode arrangement. Positive holding potentials abolished adaptation of the transducer currents, but had no influence on the time course of motion of the fibre. We have no evidence therefore that adaptation is caused by a mechanical reorganization within the bundle.

[1]  C. Hackney,et al.  Cross-links between stereocilia in the guinea pig cochlea , 1985, Hearing Research.

[2]  A. Hodgkin,et al.  The electrical response of turtle cones to flashes and steps of light , 1974, The Journal of physiology.

[3]  H. Ohmori Gating properties of the mechano‐electrical transducer channel in the dissociated vestibular hair cell of the chick. , 1987, The Journal of physiology.

[4]  A. J. Hudspeth,et al.  Compliance of the hair bundle associated with gating of mechanoelectrical transduction channels in the Bullfrog's saccular hair cell , 1988, Neuron.

[5]  H R Matthews,et al.  Role of calcium in regulating the cyclic GMP cascade of phototransduction in retinal rods. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[6]  A. J. Hudspeth,et al.  Mechanical stimulation and micromanipulation with piezoelectric bimorph elements , 1980, Journal of Neuroscience Methods.

[7]  H. Ohmori,et al.  Mechano‐electrical transduction currents in isolated vestibular hair cells of the chick. , 1985, The Journal of physiology.

[8]  D P Corey,et al.  Kinetics of the receptor current in bullfrog saccular hair cells , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  E. Neher,et al.  Potassium channels in cultured bovine adrenal chromaffin cells. , 1985, The Journal of physiology.

[10]  A. J. Hudspeth,et al.  Ionic basis of the receptor potential in a vertebrate hair cell , 1979, Nature.

[11]  L. Stryer,et al.  Highly cooperative feedback control of retinal rod guanylate cyclase by calcium ions , 1988, Nature.

[12]  F. Sigworth Electronic Design of the Patch Clamp , 1983 .

[13]  S. Bosher,et al.  Very low calcium content of cochlear endolymph, an extracellular fluid , 1978, Nature.

[14]  D P Corey,et al.  Adaptation of mechanoelectrical transduction in hair cells of the bullfrog's sacculus , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  J. O. Pickles,et al.  Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction , 1984, Hearing Research.

[16]  R. Fettiplace,et al.  Non‐linearities in the responses of turtle hair cells , 1981, The Journal of physiology.

[17]  D P Corey,et al.  Analysis of the microphonic potential of the bullfrog's sacculus , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  D P Corey,et al.  Voltage dependence of adaptation and active bundle movement in bullfrog saccular hair cells. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[19]  A J Hudspeth,et al.  The transduction channel of hair cells from the bull‐frog characterized by noise analysis. , 1986, The Journal of physiology.