Tip link loss and recovery on chick short hair cells following intense exposure to sound

2003 ◽  
Vol 181 (1-2) ◽  
pp. 40-50 ◽  
Author(s):  
Rachel Kurian ◽  
Nadia L Krupp ◽  
James C Saunders
Keyword(s):  
Hair Cells ◽  
Short Hair ◽  
Tip Link ◽  
Link Loss

scholarly journals Electrical tuning and transduction in short hair cells of the chicken auditory papilla

2013 ◽  
Vol 109 (8) ◽  
pp. 2007-2020 ◽  
Author(s):  
Xiaodong Tan ◽  
Maryline Beurg ◽  
Carole Hackney ◽  
Shanthini Mahendrasingam ◽  
Robert Fettiplace
Keyword(s):  
Hair Cells ◽  
Calcium Binding ◽  
Outer Hair Cells ◽  
Basilar Papilla ◽  
Resting Potential ◽  
Auditory Nerve Fiber ◽  
Buffer Concentration ◽  
Short Hair ◽  
Open Probability ◽  
Calbindin D

The avian auditory papilla contains two classes of sensory receptor, tall hair cells (THCs) and short hair cells (SHCs), the latter analogous to mammalian outer hair cells with large efferent but sparse afferent innervation. Little is known about the tuning, transduction, or electrical properties of SHCs. To address this problem, we made patch-clamp recordings from hair cells in an isolated chicken basilar papilla preparation at 33°C. We found that SHCs are electrically tuned by a Ca2+-activated K+ current, their resonant frequency varying along the papilla in tandem with that of the THCs, which also exhibit electrical tuning. The tonotopic map for THCs was similar to maps previously described from auditory nerve fiber measurements. SHCs also possess an A-type K+ current, but electrical tuning was observed only at resting potentials positive to −45 mV, where the A current is inactivated. We predict that the resting potential in vivo is approximately −40 mV, depolarized by a standing inward current through mechanotransducer (MT) channels having a resting open probability of ∼0.26. The resting open probability stems from a low endolymphatic Ca2+ concentration (0.24 mM) and a high intracellular mobile Ca2+ buffer concentration, estimated from perforated-patch recordings as equivalent to 0.5 mM BAPTA. The high buffer concentration was confirmed by quantifying parvalbumin-3 and calbindin D-28K with calibrated postembedding immunogold labeling, demonstrating >1 mM calcium-binding sites. Both proteins displayed an apex-to-base gradient matching that in the MT current amplitude, which increased exponentially along the papilla. Stereociliary bundles also labeled heavily with antibodies against the Ca2+ pump isoform PMCA2a.

Morphological and functional aspects of two different types of hair cells in the goldfish sacculus

1989 ◽  
Vol 62 (6) ◽  
pp. 1330-1343 ◽  
Author(s):  
I. Sugihara ◽  
T. Furukawa
Keyword(s):  
Cell Body ◽  
Hair Cells ◽  
The Other ◽  
Resting Potential ◽  
K Channel ◽  
Short Hair ◽  
Current Clamp ◽  
Other Hand ◽  
Inwardly Rectifying ◽  
A Current

1. With the use of whole-cell mode of the patch-clamp method, we examined the electrical responses of hair cells enzymatically isolated from the goldfish sacculus. 2. Hair cells from the rostral saccule had a short cell body and were ovoidal or eggplantlike in shape, whereas hair cells from the caudal saccule had a variable shape. Many had a longer cell body and were cylindrical or gourd-like in shape, but some short hair cells were also present in the caudal saccule. 3. The short hair cells had a resting potential of about -75 mV. In current-clamp experiments, these hair cells elicited damped oscillatory-potential changes of a relatively small amplitude in response to a depolarizing current. A current in the opposite direction produced a slow hyperpolarization, much larger in amplitude. 4. Resonant frequency of the short, or the oscillatory, type of hair cells ranged from 40 to 200 Hz or higher. However, resonance was generally of a poor quality as compared with that noted for hair cells in the turtle cochlea or frog sacculus. 5. The long hair cells had a resting potential of -90 to -100 mV. In current-clamp experiments, these hair cells elicited an all-or-none spike approximately 50 mV in amplitude in response to a depolarizing current. The spike was usually followed by a plateau, which was maintained for the duration of the depolarizing pulse. In some hair cells, damped slow oscillatory waves were evoked at a rate of 5-15 Hz. On the other hand, a hyperpolarizing current produced potential changes much smaller in amplitude. 6. Voltage-clamp experiments showed that Ca2+-activated K+ channel and A-current, especially its high-threshold subclass, were involved in the generation of outward rectification in the oscillatory-type hair cells. On the other hand, Na+, in addition to Ca2+, was involved in the generation of spike in the spike-type hair cells. Spike potentials were elicited even in the presence of tetrodotoxin (TTX), but the rate of rise was slower as compared with the intact spikes. 7. The spike-type hair cells had an inwardly rectifying K+ channel similar to that noted in the tunicate egg and chick vestibular hair cell. However, the oscillatory-type hair cells had an inwardly rectifying channel similar to the hyperpolarization-activated current, Ih, of the rod inner segment, or sinoatrial nodal cell, or lacked the inwardly rectifying channel. Differences in the resting membrane potential between the oscillatory- and spike-type hair cells are probably related to differences in the inwardly rectifying channels. 8. Effects of sound stimulation were simulated by injecting a half-wave rectified sinusoidal current of various frequencies.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals The development of cooperative channels explains the maturation of hair cell’s mechanotransduction

2019 ◽  
Author(s):  
Francesco Gianoli ◽  
Thomas Risler ◽  
Andrei S. Kozlov
Keyword(s):  
Ion Channels ◽  
Hair Cell ◽  
Inner Ear ◽  
Hair Cells ◽  
Hair Bundle ◽  
Mechanical Stimuli ◽  
Biophysical Properties ◽  
Tip Link ◽  
Fast Adaptation ◽  
Kinetics Of

ABSTRACTHearing relies on the conversion of mechanical stimuli into electrical signals. In vertebrates, this process of mechano-electrical transduction (MET) is performed by specialized receptors of the inner ear, the hair cells. Each hair cell is crowned by a hair bundle, a cluster of microvilli that pivot in response to sound vibrations, causing the opening and closing of mechanosensitive ion channels. Mechanical forces are projected onto the channels by molecular springs called tip links. Each tip link is thought to connect to a small number of MET channels that gate cooperatively and operate as a single transduction unit. Pushing the hair bundle in the excitatory direction opens the channels, after which they rapidly reclose in a process called fast adaptation. It has been experimentally observed that the hair cell’s biophysical properties mature gradually during postnatal development: the maximal transduction current increases, sensitivity sharpens, transduction occurs at smaller hair-bundle displacements, and adaptation becomes faster. Similar observations have been reported during tip-link regeneration after acoustic damage. Moreover, when measured at intermediate developmental stages, the kinetics of fast adaptation varies in a given cell depending on the magnitude of the imposed displacement. The mechanisms underlying these seemingly disparate observations have so far remained elusive. Here, we show that these phenomena can all be explained by the progressive addition of MET channels of constant properties, which populate the hair bundle first as isolated entities, then progressively as clusters of more sensitive, cooperative MET channels. As the proposed mechanism relies on the difference in biophysical properties between isolated and clustered channels, this work highlights the importance of cooperative interactions between mechanosensitive ion channels for hearing.SIGNIFICANCEHair cells are the sensory receptors of the inner ear that convert mechanical stimuli into electrical signals transmitted to the brain. Sensitivity to mechanical stimuli and the kinetics of mechanotransduction currents change during hair-cell development. The same trend, albeit on a shorter timescale, is also observed during hair-cell recovery from acoustic trauma. Furthermore, the current kinetics in a given hair cell depends on the stimulus magnitude, and the degree of that dependence varies with development. These phenomena have so far remained unexplained. Here, we show that they can all be reproduced using a single unifying mechanism: the progressive formation of channel pairs, in which individual channels interact through the lipid bilayer and gate cooperatively.

Mechanotransduction in vertebrate hair cells: structure and function of the stereociliary bundle

1995 ◽  
Vol 268 (1) ◽  
pp. C1-C13 ◽  
Author(s):  
C. M. Hackney ◽  
D. N. Furness
Keyword(s):  
Hair Cell ◽  
Hair Cells ◽  
Cell Function ◽  
Structure And Function ◽  
Na Channel ◽  
Tip Link ◽  
And Function ◽  
Epithelial Na Channel ◽  
Ultrastructural Findings

The mechanosensitive hair cells of the vertebrate acousticolateralis system have an apical bundle of stereocilia, deflections of which control the opening of mechano-electrical transduction channels and thus generate receptor potentials in the cell below. This review describes current theories of hair cell function in the light of recent immunocytochemical and ultrastructural findings; in particular, the location and operation of the transduction channels are considered. The most widely accepted hypothesis of mechanotransduction by hair cells is that fine extracellular links that run between the tips of shorter stereocilia and the sides of taller ones operate the transduction channels. However, the fact that the transduction channels are amiloride sensitive has led to labeling experiments using antibodies to the amiloride-sensitive epithelial Na+ channel from kidney which suggest that the mechanotransduction channels may not be directly associated with the tip links. Instead, they appear to be located near a junctionlike structure at the point of contact between the shorter and taller stereocilia. The implications of these findings for the tip link hypothesis are discussed.

Tip-link integrity and mechanical transduction in vertebrate hair cells

Neuron ◽  
1991 ◽  
Vol 7 (6) ◽  
pp. 985-994 ◽  
Author(s):  
John A. Assad ◽  
Gordon M.G. Shepherd ◽  
David P. Corey
Keyword(s):  
Hair Cells ◽  
Tip Link ◽  
Mechanical Transduction

scholarly journals Conductance and block of hair-cell mechanotransducer channels in transmembrane channel–like protein mutants

2014 ◽  
Vol 144 (1) ◽  
pp. 55-69 ◽  
Author(s):  
Maryline Beurg ◽  
Kyunghee X. Kim ◽  
Robert Fettiplace
Keyword(s):  
Hair Cells ◽  
Outer Hair Cells ◽  
Incomplete Block ◽  
Wild Type ◽  
Pharmacological Profile ◽  
Cochlear Hair Cells ◽  
Transmembrane Channel ◽  
Protein Mutants ◽  
Tip Link ◽  
Peptide Toxin

Transmembrane channel–like (TMC) proteins TMC1 and TMC2 are crucial to the function of the mechanotransducer (MT) channel of inner ear hair cells, but their precise function has been controversial. To provide more insight, we characterized single MT channels in cochlear hair cells from wild-type mice and mice with mutations in Tmc1, Tmc2, or both. Channels were recorded in whole-cell mode after tip link destruction with BAPTA or after attenuating the MT current with GsMTx-4, a peptide toxin we found to block the channels with high affinity. In both cases, the MT channels in outer hair cells (OHCs) of wild-type mice displayed a tonotopic gradient in conductance, with channels from the cochlear base having a conductance (110 pS) nearly twice that of those at the apex (62 pS). This gradient was absent, with channels at both cochlear locations having similar small conductances, with two different Tmc1 mutations. The conductance of MT channels in inner hair cells was invariant with cochlear location but, as in OHCs, was reduced in either Tmc1 mutant. The gradient of OHC conductance also disappeared in Tmc1/Tmc2 double mutants, in which a mechanically sensitive current could be activated by anomalous negative displacements of the hair bundle. This “reversed stimulus–polarity” current was seen with two different Tmc1/Tmc2 double mutants, and with Tmc1/Tmc2/Tmc3 triple mutants, and had a pharmacological sensitivity comparable to that of native MT currents for most antagonists, except dihydrostreptomycin, for which the affinity was less, and for curare, which exhibited incomplete block. The existence in the Tmc1/Tmc2 double mutants of MT channels with most properties resembling those of wild-type channels indicates that proteins other than TMCs must be part of the channel pore. We suggest that an external vestibule of the MT channel may partly account for the channel’s large unitary conductance, high Ca2+ permeability, and pharmacological profile, and that this vestibule is disrupted in Tmc mutants.

scholarly journals Tmc Reliance Is Biased by the Hair Cell Subtype and Position Within the Ear

2021 ◽  
Vol 8 ◽  
Author(s):  
Shaoyuan Zhu ◽  
Zongwei Chen ◽  
Haoming Wang ◽  
Brian M. McDermott
Keyword(s):  
Hair Cell ◽  
Hair Cells ◽  
Cell Types ◽  
Genetic Mutations ◽  
Mechanical Stimuli ◽  
Vestibular Organ ◽  
Short Hair ◽  
Transmembrane Channel ◽  
Quantitative Measurements ◽  
Cell Position

Hair cells are heterogenous, enabling varied roles in sensory systems. An emerging hypothesis is that the transmembrane channel-like (Tmc) proteins of the hair cell’s mechanotransduction apparatus vary within and between organs to permit encoding of different mechanical stimuli. Five anatomical variables that may coincide with different Tmc use by a hair cell within the ear are the containing organ, cell morphology, cell position within an organ, axis of best sensitivity for the cell, and the hair bundle’s orientation within this axis. Here, we test this hypothesis in the organs of the zebrafish ear using a suite of genetic mutations. Transgenesis and quantitative measurements demonstrate two morphologically distinct hair cell types in the central thickness of a vestibular organ, the lateral crista: short and tall. In contrast to what has been observed, we find that tall hair cells that lack Tmc1 generally have substantial reductions in mechanosensitivity. In short hair cells that lack Tmc2 isoforms, mechanotransduction is largely abated. However, hair cell Tmc dependencies are not absolute, and an exceptional class of short hair cell that depends on Tmc1 is present, termed a short hair cell erratic. To further test anatomical variables that may influence Tmc use, we map Tmc1 function in the saccule of mutant larvae that depend just on this Tmc protein to hear. We demonstrate that hair cells that use Tmc1 are found in the posterior region of the saccule, within a single axis of best sensitivity, and hair bundles with opposite orientations retain function. Overall, we determine that Tmc reliance in the ear is dependent on the organ, subtype of hair cell, position within the ear, and axis of best sensitivity.

Sign in / Sign up

Export Citation Format

Share Document