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Dive into the research topics where Andrei S. Kozlov is active.

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Featured researches published by Andrei S. Kozlov.


The Journal of Neuroscience | 2004

Glutamate Released from Glial Cells Synchronizes Neuronal Activity in the Hippocampus

María Cecilia Angulo; Andrei S. Kozlov; Serge Charpak; Etienne Audinat

Glial cells of the nervous system directly influence neuronal and synaptic activities by releasing transmitters. However, the physiological consequences of this glial transmitter release on brain information processing remain poorly understood. We demonstrate here in hippocampal slices of 2- to 5-week-old rats that glutamate released from glial cells generates slow transient currents (STCs) mediated by the activation of NMDA receptors in pyramidal cells. STCs persist in the absence of neuronal and synaptic activity, indicating a nonsynaptic origin of the source of glutamate. Indeed, STCs occur spontaneously but can also be induced by pharmacological tools known to activate astrocytes and by the selective mechanical stimulation of single nearby glial cells. Bath application of the inhibitor of the glutamate uptake dl-threo-β-benzyloxyaspartate increases both the frequency of STCs and the amplitude of a tonic conductance mediated by NMDA receptors and probably also originated from glial glutamate release. By using dual recordings, we observed synchronized STCs in pyramidal cells having their soma distant by <100 μm. The degree of precision (<100 msec) of this synchronization rules out the involvement of calcium waves spreading through the glial network. It also indicates that single glial cells release glutamate onto adjacent neuronal processes, thereby controlling simultaneously the excitability of several neighboring pyramidal cells. In conclusion, our results show that the glial glutamate release occurs spontaneously and synchronizes the neuronal activity in the hippocampus.


European Journal of Neuroscience | 1999

Distinct kinetics of cloned T-type Ca2 + channels lead to differential Ca2 + entry and frequency-dependence during mock action potentials.

Andrei S. Kozlov; Frank McKenna; Jung-Ha Lee; Leanne L. Cribbs; Edward Perez-Reyes; Anne Feltz; Régis C. Lambert

Voltage‐dependent activity around the resting potential is determinant in neuronal physiology and participates in the definition of the firing pattern. Low‐voltage‐activated T‐type Ca2 +  channels directly affect the membrane potential and control a number of secondary Ca2 + ‐dependent permeabilities. We have studied the ability of the cloned T‐type channels (α1G,H,I) to carry Ca2 +  currents in response to mock action potentials. The relationship between the spike duration and the current amplitude is specific for each of the T‐type channels, reflecting their individual kinetic properties. Typically the charge transfer increases with spike broadening, but the total Ca2 +  entry saturates at different spike durations according to the channel type: 4 ms for α1G; 7 ms for α1H; and >  10 ms for α1I channels. During bursts, currents are inhibited and/or transiently potentiated according to the α1 channel type, with larger effects at higher frequency. The inhibition may be induced by voltage‐independent transitions toward inactivated states and/or channel inactivation through intermediate closed states. The potentiation is explained by an acceleration in the channel activation kinetics. Relatively fast inactivation and slow recovery limit the ability of α1G and α1H channels to respond to high frequency stimulation ( >  20 Hz). In contrast, the slow inactivation of α1I subunits allows these channels to continue participating in high frequency bursts (100 Hz). The biophysical properties of α1G, H and I channels will therefore dramatically modulate the effect of neuronal activities on Ca2 +  signalling.


Nature Neuroscience | 2007

Coherent motion of stereocilia assures the concerted gating of hair-cell transduction channels

Andrei S. Kozlov; Thomas Risler; A. J. Hudspeth

The hair cells mechanoreceptive organelle, the hair bundle, is highly sensitive because its transduction channels open over a very narrow range of displacements. The synchronous gating of transduction channels also underlies the active hair-bundle motility that amplifies and tunes responsiveness. The extent to which the gating of independent transduction channels is coordinated depends on how tightly individual stereocilia are constrained to move as a unit. Using dual-beam interferometry in the bullfrogs sacculus, we found that thermal movements of stereocilia located as far apart as a hair bundles opposite edges showed high coherence and negligible phase lag. Because the mechanical degrees of freedom of stereocilia are strongly constrained, a force applied anywhere in the hair bundle deflects the structure as a unit. This feature assures the concerted gating of transduction channels that maximizes the sensitivity of mechanoelectrical transduction and enhances the hair bundles capacity to amplify its inputs.


Nature | 2011

Forces between clustered stereocilia minimize friction in the ear on a subnanometre scale

Andrei S. Kozlov; Johannes Baumgart; Thomas Risler; Corstiaen P. C. Versteegh; A. J. Hudspeth

The detection of sound begins when energy derived from an acoustic stimulus deflects the hair bundles on top of hair cells. As hair bundles move, the viscous friction between stereocilia and the surrounding liquid poses a fundamental physical challenge to the ear’s high sensitivity and sharp frequency selectivity. Part of the solution to this problem lies in the active process that uses energy for frequency-selective sound amplification. Here we demonstrate that a complementary part of the solution involves the fluid–structure interaction between the liquid within the hair bundle and the stereocilia. Using force measurement on a dynamically scaled model, finite-element analysis, analytical estimation of hydrodynamic forces, stochastic simulation and high-resolution interferometric measurement of hair bundles, we characterize the origin and magnitude of the forces between individual stereocilia during small hair-bundle deflections. We find that the close apposition of stereocilia effectively immobilizes the liquid between them, which reduces the drag and suppresses the relative squeezing but not the sliding mode of stereociliary motion. The obliquely oriented tip links couple the mechanotransduction channels to this least dissipative coherent mode, whereas the elastic horizontal top connectors that stabilize the structure further reduce the drag. As measured from the distortion products associated with channel gating at physiological stimulation amplitudes of tens of nanometres, the balance of viscous and elastic forces in a hair bundle permits a relative mode of motion between adjacent stereocilia that encompasses only a fraction of a nanometre. A combination of high-resolution experiments and detailed numerical modelling of fluid–structure interactions reveals the physical principles behind the basic structural features of hair bundles and shows quantitatively how these organelles are adapted to the needs of sensitive mechanotransduction.


Molecular and Cellular Biology | 2010

Highly Specific Alternative Splicing of Transcripts Encoding BK Channels in the Chicken's Cochlea Is a Minor Determinant of the Tonotopic Gradient†

Soledad Miranda-Rottmann; Andrei S. Kozlov; A. J. Hudspeth

ABSTRACT The frequency sensitivity of auditory hair cells in the inner ear varies with their longitudinal position in the sensory epithelium. Among the factors that determine the differential cellular response to sound is the resonance of a hair cells transmembrane electrical potential, whose frequency correlates with the kinetic properties of the high-conductance Ca2+-activated K+ (BK) channels encoded by a Slo (kcnma1) gene. It has been proposed that the inclusion of specific alternative axons in the Slo transcripts along the cochlea underlies the gradient of BK-channel kinetics. By analyzing the complete sequences of chicken Slo gene (cSlo) cDNAs from the chickens cochlea, we show that most transcripts lack alternative exons. Transcripts with more than one alternative exon constitute only 10% of the total. Although the fraction of transcripts containing alternative exons increases from the cochlear base to the apex, the combination of alternative exons is not regulated. There is also a clear increase in the expression of BK transcripts with long carboxyl termini toward the apex. When long and short BK transcripts are expressed in HEK-293 cells, the kinetics of single-channel currents differ only slightly, but they are substantially slowed when the channels are coexpressed with the auxiliary β subunit that occurs more widely at the apex. These results argue that the tonotopic gradient is not established by the selective inclusion of highly specific cSlo exons. Instead, a gradient in the expression of β subunits slows BK channels toward the low-frequency apex of the cochlea.


The Journal of Neuroscience | 2007

The Structural and Functional Differentiation of Hair Cells in a Lizard's Basilar Papilla Suggests an Operational Principle of Amniote Cochleas

M. Eugenia Chiappe; Andrei S. Kozlov; A. J. Hudspeth

The hair cells in the mammalian cochlea are of two distinct types. Inner hair cells are responsible for transducing mechanical stimuli into electrical responses, which they forward to the brain through a copious afferent innervation. Outer hair cells, which are thought to mediate the active process that sensitizes and tunes the cochlea, possess a negligible afferent innervation. For every inner hair cell, there are approximately three outer hair cells, so only one-quarter of the hair cells directly deliver information to the CNS. Although this is a surprising feature for a sensory system, the occurrence of a similar innervation pattern in birds and crocodilians suggests that the arrangement has an adaptive value. Using a lizard with highly developed hearing, the tokay gecko, we demonstrate in the present study that the same principle operates in a third major group of terrestrial animals. We propose that the differentiation of hair cells into signaling and amplifying classes reflects incompatible strategies for the optimization of mechanoelectrical transduction and of an active process based on active hair-bundle motility.


Proceedings of the National Academy of Sciences of the United States of America | 2012

Anomalous Brownian motion discloses viscoelasticity in the ear’s mechanoelectrical-transduction apparatus

Andrei S. Kozlov; Daniel Andor-Ardó; A. J. Hudspeth

The ear detects sounds so faint that they produce only atomic-scale displacements in the mechanoelectrical transducer, yet thermal noise causes fluctuations larger by an order of magnitude. Explaining how hearing can operate when the magnitude of the noise greatly exceeds that of the signal requires an understanding both of the transducer’s micromechanics and of the associated noise. Using microrheology, we characterize the statistics of this noise; exploiting the fluctuation-dissipation theorem, we determine the associated micromechanics. The statistics reveal unusual Brownian motion in which the mean square displacement increases as a fractional power of time, indicating that the mechanisms governing energy dissipation are related to those of energy storage. This anomalous scaling contradicts the canonical model of mechanoelectrical transduction, but the results can be explained if the micromechanics incorporates viscoelasticity, a salient characteristic of biopolymers. We amend the canonical model and demonstrate several consequences of viscoelasticity for sensory coding.


Proceedings of the National Academy of Sciences of the United States of America | 2016

Central auditory neurons have composite receptive fields

Andrei S. Kozlov; Timothy Q. Gentner

Significance How neurons are selective for complex natural stimuli remains poorly understood, in part because standard statistical tools only identify one or two features of stimuli but not complete sets. Here, using a statistical method that overcomes these difficulties, we demonstrate that a set of multiple distinct acoustical features exists in individual auditory neurons in songbirds. We then use birdsongs to train an unsupervised neural network constrained by two common properties of biological neural circuits. The network rediscovers the same stimulus features observed in vivo. These results demonstrate that individual high-level auditory neurons respond not to single, but to multiple features of natural stimuli. This enables a robust, statistically optimal, representation of complex, real-world signals such as birdsong, speech, or music. High-level neurons processing complex, behaviorally relevant signals are sensitive to conjunctions of features. Characterizing the receptive fields of such neurons is difficult with standard statistical tools, however, and the principles governing their organization remain poorly understood. Here, we demonstrate multiple distinct receptive-field features in individual high-level auditory neurons in a songbird, European starling, in response to natural vocal signals (songs). We then show that receptive fields with similar characteristics can be reproduced by an unsupervised neural network trained to represent starling songs with a single learning rule that enforces sparseness and divisive normalization. We conclude that central auditory neurons have composite receptive fields that can arise through a combination of sparseness and normalization in neural circuits. Our results, along with descriptions of random, discontinuous receptive fields in the central olfactory neurons in mammals and insects, suggest general principles of neural computation across sensory systems and animal classes.


Current Biology | 2016

Comparative Aspects of Hearing in Vertebrates and Insects with Antennal Ears

Joerg T. Albert; Andrei S. Kozlov

The evolution of hearing in terrestrial animals has resulted in remarkable adaptations enabling exquisitely sensitive sound detection by the ear and sophisticated sound analysis by the brain. In this review, we examine several such characteristics, using examples from insects and vertebrates. We focus on two strong and interdependent forces that have been shaping the auditory systems across taxa: the physical environment of auditory transducers on the small, subcellular scale, and the sensory-ecological environment within which hearing happens, on a larger, evolutionary scale. We briefly discuss acoustical feature selectivity and invariance in the central auditory system, highlighting a major difference between insects and vertebrates as well as a major similarity. Through such comparisons within a sensory ecological framework, we aim to emphasize general principles underlying acute sensitivity to airborne sounds.


The Journal of Physiology | 2012

Relative stereociliary motion in a hair bundle opposes amplification at distortion frequencies

Andrei S. Kozlov; Thomas Risler; Armin J. Hinterwirth; A. J. Hudspeth

Non‐technical summary  The hair cell, or sensory receptor of the inner ear, achieves high sensitivity by amplifying its mechanical inputs. The mechanism of amplification depends on the concerted opening and closing of mechanically sensitive ion channels in the hair bundle, a cluster of actin‐containing rods that protrude from the cells top surface. When a hair cell is stimulated simultaneously at two frequencies, channel gating also produces distortion products or responses at other frequencies. Using a sensitive interferometer to measure the motions of stereocilia, we have found that hydrodynamic forces act within the hair bundle to suppress these spurious signals. The hair bundle has evidently evolved an effective means of amplifying input signals while reducing the effect of distortions.

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A. J. Hudspeth

Howard Hughes Medical Institute

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Etienne Audinat

Paris Descartes University

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Anne Feltz

Centre national de la recherche scientifique

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Régis C. Lambert

Centre national de la recherche scientifique

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Julien Hering

École Normale Supérieure

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