Cell Reports,
Journal Year:
2020,
Volume and Issue:
31(13), P. 107844 - 107844
Published: June 1, 2020
Changes
in
dendritic
morphology
response
to
activity
have
long
been
thought
be
a
critical
component
of
how
neural
circuits
develop
properly
encode
sensory
information.
Ventral-preferring
direction-selective
ganglion
cells
(vDSGCs)
asymmetric
dendrites
oriented
along
their
preferred
direction,
and
this
has
hypothesized
play
role
tuning.
Here
we
report
the
surprising
result
that
visual
experience
is
for
alignment
vDSGC
direction.
Interestingly,
vDSGCs
dark-reared
mice
lose
inhibition-independent
contribution
tuning
while
maintaining
inhibitory
input.
These
data
indicate
different
mechanisms
cell's
computational
abilities
can
constructed
over
development
through
divergent
mechanisms.
Cell Reports,
Journal Year:
2021,
Volume and Issue:
37(11), P. 110106 - 110106
Published: Dec. 1, 2021
Retinal
bipolar
cells
are
second-order
neurons
that
transmit
basic
features
of
the
visual
scene
to
postsynaptic
partners.
However,
their
contribution
motion
detection
has
not
been
fully
appreciated.
Here,
we
demonstrate
cholinergic
feedback
from
starburst
amacrine
(SACs)
certain
presynaptic
via
alpha-7
nicotinic
acetylcholine
receptors
(α7-nAChRs)
promotes
direction-selective
signaling.
Patch
clamp
recordings
reveal
distinct
cell
types
making
synapses
at
proximal
SAC
dendrites
also
express
α7-nAChRs,
producing
directionally
skewed
excitatory
inputs.
Asymmetric
excitation
contributes
in
On-Off
ganglion
(On-Off
DSGCs),
predicted
by
computational
modeling
and
supported
patch
DSGCs
when
α7-nAChRs
is
eliminated
pharmacologically
or
conditional
knockout.
Altogether,
these
results
show
enhances
signaling
SACs
DSGCs,
illustrating
how
provide
a
scaffold
for
microcircuits
cooperatively
enhance
retinal
detection.
Current Biology,
Journal Year:
2022,
Volume and Issue:
32(11), P. 2529 - 2538.e4
Published: May 18, 2022
The
detection
of
motion
direction
is
a
fundamental
visual
function
and
classic
model
for
neural
computation.
In
the
non-primate
retina,
selectivity
arises
in
starburst
amacrine
cell
(SAC)
dendrites,
which
provide
selective
inhibition
to
direction-selective
retinal
ganglion
cells
(dsRGCs).
Although
SACs
are
present
primates,
their
connectivity
existence
dsRGCs
remain
open
questions.
Here,
we
connectomic
reconstruction
primate
ON
SAC
circuit
from
serial
electron
microscopy
volume
macaque
central
retina.
We
show
that
structural
basis
SACs'
ability
confer
directional
on
postsynaptic
neurons
conserved.
selectively
target
candidate
homolog
mammalian
ON-sustained
project
accessory
optic
system
(AOS)
contribute
gaze-stabilizing
reflexes.
These
results
indicate
capacity
compute
earlier
than
classically
thought.
Cell Reports,
Journal Year:
2020,
Volume and Issue:
31(5), P. 107608 - 107608
Published: May 1, 2020
An
antagonistic
center-surround
receptive
field
is
a
key
feature
in
sensory
processing,
but
how
it
contributes
to
specific
computations
such
as
direction
selectivity
often
unknown.
Retinal
On-starburst
amacrine
cells
(SACs),
which
mediate
direction-selective
ganglion
(DSGCs),
exhibit
organization:
depolarizing
light
increments
and
decrements
their
center
surround,
respectively.
We
find
that
repetitive
stimulation
exhausts
SAC
enhances
its
surround
use
study
responses
contribute
selectivity.
Center,
not
activation
induces
SACs.
Nevertheless,
both
elicited
DSGCs,
opposite
directions.
Physiological
modeling
data
suggest
the
opposing
can
result
from
inverted
temporal
balance
between
excitation
inhibition
implying
SAC's
response
timing
dictates
Our
findings
reveal
mechanisms
for
demonstrate
context-dependent
reorganization
enables
flexible
computations.
The Journal of Comparative Neurology,
Journal Year:
2025,
Volume and Issue:
533(1)
Published: Jan. 1, 2025
ABSTRACT
Direction
selectivity
is
a
fundamental
feature
in
the
visual
system.
In
retina,
direction
independently
computed
by
ON
and
OFF
circuits.
However,
advantages
of
extracting
directional
information
from
these
two
independent
circuits
are
unclear.
To
gain
insights,
we
examined
ON–OFF
direction‐selective
ganglion
cells
(DSGCs),
which
recombine
signals
both
Specifically,
investigated
dendritic
architecture
neurons
with
premise
that
asymmetries
will
provide
insights
into
function.
Scrutinizing
dendrites
dye‐filled
DSGCs
reveals
arbors
substantially
denser.
The
increase
density
can
be
primarily
attributed
to
higher
branching
seen
arbors.
Further,
analysis
previously
published
serial
block‐face
electron
microscopy
dataset
revealed
denser
packed
more
bipolar
synapses
per
unit
length.
These
suggest
DSGC
preferentially
magnifies
synaptic
drive
pathway,
potentially
allowing
it
encode
distinct
pathway.
While
multicompartment
models
have
long
been
used
to
study
the
biophysics
of
neurons,
it
is
still
challenging
infer
parameters
such
from
data
including
uncertainty
estimates.
Here,
we
performed
Bayesian
inference
for
detailed
neuron
a
photoreceptor
and
an
OFF-
ON-cone
bipolar
cell
mouse
retina
based
on
two-photon
imaging
data.
We
obtained
multivariate
posterior
distributions
specifying
plausible
parameter
ranges
consistent
with
allowing
identify
poorly
constrained
by
To
demonstrate
potential
mechanistic
data-driven
models,
created
simulation
environment
external
electrical
stimulation
optimized
stimulus
waveforms
target
cells,
current
major
problem
retinal
neuroprosthetics.
Across
species,
the
optokinetic
reflex
(OKR)
stabilizes
vision
during
self-motion.
OKR
occurs
when
ON
direction-selective
retinal
ganglion
cells
(oDSGCs)
detect
slow,
global
image
motion
on
retina.
How
oDSGC
activity
is
integrated
centrally
to
generate
behavior
remains
unknown.
Here,
we
discover
mechanisms
that
contribute
encoding
in
vertically
tuned
oDSGCs
and
leverage
these
findings
empirically
define
signal
transformation
between
output
vertical
behavior.
We
demonstrate
contrast-sensitive
asymmetric
for
types
prefer
opposite
directions.
These
phenomena
arise
from
interplay
spike
threshold
nonlinearities
differences
synaptic
input
weights,
including
shifts
balance
of
excitation
inhibition.
In
behaving
mice,
neurophysiological
observations,
along
with
a
central
subtraction
outputs,
accurately
predict
trajectories
across
stimulus
conditions.
Thus,
tuning
competing
sensory
channels
can
critically
shape
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 11, 2024
Summary
paragraph
GABA
(
ψ
-aminobutyric
acid)
is
the
primary
inhibitory
neurotransmitter
in
mammalian
central
nervous
system
(CNS)
1,2
.
There
a
wide
range
of
GABAergic
neuronal
types,
each
which
plays
an
important
role
neural
processing
and
etiology
neurological
disorders
3–5
However,
there
no
comprehensive
understanding
this
functional
diversity,
due
to
lack
genetic
tools
target
study
multitude
cell
types.
Here
we
perform
two-photon
imaging
release
inner
plexiform
layer
(IPL)
mouse
retina
using
newly
developed
sensor
iGABASnFR2.
By
applying
varied
light
stimuli
isolated
retinae,
reveal
over
40
different
GABA-releasing
neurons,
including
some
not
previously
described.
Individual
types
show
unique
distributions
synaptic
sites
sublayers
comprising
IPL,
allowing
layer-specific
visual
encoding.
Synaptic
input
output
are
aligned
along
specific
retinal
orientations
for
multiple
Furthermore,
computational
modeling
reveals
that
combination
type-specific
spatial
structure
kinetics
enables
neurons
suppress
sculpt
excitatory
signals
response
behaviorally
relevant
motion
structures.
Our
high-throughput
approach
provides
first
physiological
characterization
signaling
vertebrate
CNS.
Future
applications
method
will
enable
interrogation
function
dysfunction
diverse
circuits
health
disease.
Current Biology,
Journal Year:
2022,
Volume and Issue:
32(10), P. 2130 - 2143.e3
Published: April 7, 2022
The
sensory
periphery
is
responsible
for
detecting
ethologically
relevant
features
of
the
external
world,
using
compact,
predominantly
feedforward
circuits.
Visual
motion
a
particularly
prevalent
feature,
presence
which
can
be
signal
to
enact
diverse
behaviors
ranging
from
gaze
stabilization
reflexes
predator
avoidance
or
prey
capture.
To
understand
how
retina
constructs
distinct
neural
representations
required
these
behaviors,
we
investigated
two
circuits
encoding
different
aspects
image
motion:
ON
and
ON-OFF
direction-selective
ganglion
cells
(DSGCs).
Using
combination
two-photon
targeted
whole-cell
electrophysiology,
pharmacology,
conditional
knockout
mice,
show
that
inhibitory
pathways
independently
control
tuning
velocity
direction
in
cell
types.
We
further
employ
dynamic
clamp
numerical
modeling
techniques
asymmetric
inhibition
provides
velocity-invariant
mechanism
directional
tuning,
despite
strong
dependence
classical
models
selectivity.
therefore
demonstrate
invariant
by
interneurons
act
as
computational
building
blocks
construct
distinct,
behaviorally
signals
at
earliest
stages
visual
system.
Annual Review of Vision Science,
Journal Year:
2021,
Volume and Issue:
7(1), P. 105 - 128
Published: Sept. 15, 2021
Our
sense
of
sight
relies
on
photoreceptors,
which
transduce
photons
into
the
nervous
system's
electrochemical
interpretation
visual
world.
These
precious
photoreceptors
can
be
disrupted
by
disease,
injury,
and
aging.
Once
start
to
die,
but
before
blindness
occurs,
remaining
retinal
circuitry
withstand,
mask,
or
exacerbate
photoreceptor
deficit
potentially
receptive
newfound
therapies
for
vision
restoration.
To
maximize
retina's
receptivity
therapy,
one
must
understand
conditions
that
influence
state
retina.
In
this
review,
we
provide
an
overview
structure
function
in
health
disease.
We
analyze
a
collection
observations
disruption
generate
predictive
model
identify
parameters
response.
Finally,
speculate
whether
retina,
with
its
remarkable
capacity
over
light
levels
spanning
nine
orders
magnitude,
uses
these
same
adaptational
mechanisms
withstand
perhaps
mask
loss.