Salamanca Study Abroad Program: Neurobiology of Hearing
Transcript of Salamanca Study Abroad Program: Neurobiology of Hearing
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Salamanca Study Abroad Program:
Neurobiology of Hearing
Synaptics and the auditory nerve
R. Keith Duncan
University of Michigan
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Review Resources
Reviews:
Safieddine et al., 2012, The auditory hair cell ribbon synapse: From assembly to function, Ann Rev Neurosci, 35:509-528
Kim et al., 2013, Single Ca2+ channels and exocytosis at sensory synapses, J Physiol, epub
Note: this is an excellent review describing the differences between cochlear and retinal ribbon synapses.
Rabbitt and Brownell, 2011 Efferent modulation of hair cell function, Curr Opinion Otolaryngol Head Neck Surg,19:376-381
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Outline
Exocytosis and synaptics
Afferent physiology
Efferent physiology
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4
Type 1 afferents:
• 95% of cochlear afferents
• account for hearing
• each innervates only 1 IHC
• ~20 innervate one IHC
Type 2 afferents:
• less well-described
• en passant innervation of OHCs;
Afferent cochlear innervation
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Hair cells form ribbon synapses with
afferent neurons
5
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Distinct pools of vesicles
• Electron tomography
reconstruction shows 4 pools
Ribbon docked vesicles
(readily releasable pool, ~10)
Tethered vesicles (releasable
pool, ~200)
Extrasynaptic docked
vesicles
Cytoplasmic vesicles
(recruitable pool?)
• These pools likely contribute to
distinct kinetics of exocytosis as
stimulus duration increases.Lenzi & von Gersdorff, 2001
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Distinct phases of exocytosis
Capacitance is a proxy for
exocytosis. Vesicle fusion
increases surface area which
increases capacitance.
(see supplemental slides)
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Exocytosis occurs in calcium
nanodomains
Hair cells
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The synaptic vesicle cycleNT uptake, translocation, docking
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Molecular Components of Ribbon Synapses
Differ from Conventional Synapses
Vesicle related:
• Synaptotagmins are the Ca2+ sensors in most
synapses. Mature hair cells lack SYT I and II
but have IV, VI-IX (rare types). Otoferlin
appears to act as Ca2+ sensor.
• Hair cells express Rab/RabBP, VAMP1, but not
synapsins or complexins
Core-complex related:
• Syntaxin 1A and SNAP-25 is present
• Munc13 is missing. Otoferlin may replace
priming role of Munc13.
Lenzi et al., 1999
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Methods to study post-synaptic
response
Glowatzki and Fuchs, 2002
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Primary Afferents are Glutamatergic
Red: Ribeye (Ctbp2)
Green: GluR2/3
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Post-synaptic potentials span a wide range
of amplitudes, not a train of miniEPSCs
Whole-cell voltage-clamp
Vhold = -94 mV
Inward current
Most monophasic
(coordinated release)
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Multivesicular release
Similar distribution if hair cell bathed in
5 mM K+ or 40 mM.
Frequency of EPSCs increased but
amplitude range unchanged.
True miniEPSC ~40pA
Mean amplitude ~150pA (4 vesicles)
Max amplitude ~800pA (20 vesicles)
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Ribbons vs Conventional Synapse:
Quantal yet multivesicular
Multivesicular release = large ave. EPSC
Bouton has very high input resistance.
EPSP ~ EPSC * Rin
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Stimulus Features Coded by the
Auditory Nerve
How does the auditory nerve encode:
Frequency?
Intensity?
Time?
Pure-tones vs complex stimuli?
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Response to Tone Bursts:
Peristimulus Time Histograms (PSTH)
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“Receptive Field” of an auditory neuron:
Tuning Curves and Spectral Response Plots
Saunders et al., 1996: Auditory nerve responses from chick cochlea
Frequency (kHz)0.1 1 4
Use tone pips/bursts.
Vary frequency and intensity.
Record driven spike-rate.
Salient features:
• Iso-response contour or
“tuning curve”
• Threshold (i.e. 26 dB)
• Best Frequency (i.e. 0.8
kHz)
10.1 10.1
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Response to Frequency: Place Coding
How to generate a tonotopic map
Inject tracer
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Response to Intensity: RI functions
INTENSITY (dB)
SP
IKE
RA
TE
(S
pik
es
/S)
Tone Burst
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Response to Intensity:Threshold Varies with Spontaneous Rate
HSR
• 60% of primary afferents
• > 18 spikes/s; low threshold
• Steep rate-intensity function;
narrow dynamic range (20-30 dB)
• Broadly tuned
MSR
• 25% of afferents
• Between 0.5 and 18 spikes/s
• Sloping-saturation RI function
LSR
• 15% of afferents
• < 0.5 spikes/s; high threshold
• Shallow sloping RI function; large
dynamic range (>60 dB)
• Sharply tuned
Why this diversity of RI types?
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Spontaneous Rate:
Multi-modal Distribution
Liberman, 1978: Auditory nerve responses from cats
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Response to Intensity:Mechanistic View of Spontaneous Rate
Models suggest SR differences are presynaptic – differences in calcium current density (Sumner et al., 2002).
Patch-clamp of the hair cell shows non-uniform distribution of calcium channels (singles, groups of 2-15, groups of 20-80) (Rodriguez-Contreras and Yamoah, 2001; Frank et al., 2009).
How is the size of the active zone, density of calcium channels, and presynaptic strength controlled?
HSR
MSR
LSR
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Response to Complex Stimuli:A place code theory that implies a key use for high threshold neurons
F1-3 are formant frequencies for the vowel sound “eh”
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It’s a two-way street
afferent
efferent
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Efferent innervation in the cochlea
Efferents from
medial olivocochlear
system (bilaterally)
synapse onto
several OHCs.
Efferents from lateral
olivocochlear system
synapse onto hair
cell early in
development and
then onto the Type I
afferent bouton.
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LOC fibers regulate afferent sensitivity
Less well understood
What neurotransmitters are released?
What effects? When activated, the LOC elicits
either slow excitation or suppression of cochlear output.
Putative roles include protection from excitotoxicity from noise, gain control, and binaural adjustment of sensitivity for sound localization cues.
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Stimulation of MOC fibers reduces
cochlear sensitivity
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MOC Inhibition:
Two channel hypothesis
• MOC efferents release ACh.
• Ca2+ influx activates SK/BK.
• K+ efflux hyperpolarizes hair cell.
• Hyperpolarization would enhance
the drive on transduction but shift
operating range of the cochlear
amplifier.
K+, SK
Ca2+,
AChR
ACh
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MOC efferents
Wersinger and Fuchs, 2011
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Open questions
What underlies the diverse dynamic ranges of spont. rates in
Type I afferents?
How is the number and localization of calcium channels
controlled at the hair cell ribbon synapse (and compare with
retina ribbon synapse)? Is there a role for palmitoylation of
beta2 calcium channel subunits?
What is the functional role of Type II afferents?
Are complex sound spectra encoded by fine temporal structure
or high-threshold fibers at loud sound levels?
What roles do other neurotransmitters have in efferent system
(GABA, CGRP, etc)?
Does the LOC enable ‘Gain control’ of the auditory periphery?
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Supplementary material
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Itotal = IR + ICwhere IR is current through the resistive arm
and IC is current through the capacitor
Cu
rren
t
Time IRIC
Volt
age
Note 90o phase shift between IR and IC allowing
each I to be monitored or determined
separately using a lock-in amplifier
The amplitude of the Cm current is dependent
upon the cell surface area. (~ 1 mF/cm2).
Time-resolved Membrane
Capacitance Measurements
Ra
Rseal
Rm Cm
dt
dVCEV
RtI m
mrm
m
1
)(
Now, under voltage-clamp, stimulate with a
sine wave. Capacitive current will vary as
cosine.
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The discharges of cochlear nerve fibres to
low-frequency sounds are not random;
they occur at particular times (phase locking).
Evans (1975)
Phase-locking
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Intensity coding preserved in phase-
locked responses
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Response to Time: Phase-locking
Depends on Stimulus Frequency
In vivo intracellular
recording from a hair cell.
The ability of the auditory nerve to
synchronize to the sound stimulus is
dependent on the stimulus frequency.
However, there are limits to this coding
modality, due to:
• Capacitance of the hair cell
membrane (LPF cutoff ~ 2 kHz)
• Maximum spike rate of a neuron is
around 1000 kHz.
Auditory neurons show robust phase-
locked responses up to 4 kHz.
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Phasic Responses in High-Frequency
Neurons
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Phasic Responses in High-Frequency
Neurons Driven at Low-Frequencies