The
processing
of
visual
information
by
retinal
starburst
amacrine
cells
(SACs)
involves
transforming
excitatory
input
from
bipolar
(BCs)
into
directional
calcium
output.
While
previous
studies
have
suggested
that
an
asymmetry
in
the
kinetic
properties
along
soma-dendritic
axes
postsynaptic
cell
could
enhance
tuning
at
level
individual
branches,
it
remains
unclear
whether
biologically
relevant
presynaptic
kinetics
contribute
to
direction
selectivity
when
stimulation
engages
entire
dendritic
tree.
To
address
this
question,
we
built
multicompartmental
models
bipolar–SAC
circuit
and
trained
them
boost
tuning.
We
report
despite
significant
crosstalk
dissimilar
preferences
dendrites
occur
during
whole-cell
stimulation,
rules
guide
BC
leading
optimal
are
similar
single-dendrite
condition.
correlate
model
predictions
empirical
findings,
utilized
two-photon
glutamate
imaging
study
dynamics
release
onto
ON-
OFF-starburst
murine
retina.
reveal
diverse
response
motion
both
populations;
algorithms
on
experimental
data
differences
temporal
likely
correspond
heterogeneous
receptive
field
(RF)
among
different
types,
including
spatial
extent
center
surround
components.
In
addition,
demonstrate
architecture
composed
units
with
experimentally
recorded
drive
but
not
levels
replicate
suggesting
other
DS
mechanisms
required
explain
SAC
function.
Our
provides
new
insights
complex
underlying
highlights
potential
contribution
computation
cells.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Jan. 18, 2024
Abstract
In
early
sensory
systems,
cell-type
diversity
generally
increases
from
the
periphery
into
brain,
resulting
in
a
greater
heterogeneity
of
responses
to
same
stimuli.
Surround
suppression
is
canonical
visual
computation
that
begins
within
retina
and
found
at
varying
levels
across
retinal
ganglion
cell
types.
Our
results
show
level
surround
occurs
subcellularly
bipolar
synapses.
Using
single-cell
electrophysiology
serial
block-face
scanning
electron
microscopy,
we
two
types
exhibit
very
different
even
though
they
receive
input
This
divergence
signal
through
synapse-specific
regulation
by
amacrine
cells
scale
tens
microns.
These
findings
indicate
each
synapse
single
can
carry
unique
signal,
expanding
number
possible
functional
channels
earliest
stages
processing.
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.
Visual Neuroscience,
Journal Year:
2023,
Volume and Issue:
40
Published: Jan. 1, 2023
Abstract
In
a
recent
study,
visual
signals
were
recorded
for
the
first
time
in
starburst
amacrine
cells
of
macaque
retina,
and,
as
mouse
and
rabbit,
directional
bias
observed
calcium
was
from
near
dendritic
tips.
Stimulus
motion
soma
toward
tip
generated
larger
signal
than
soma.
Two
mechanisms
affecting
spatiotemporal
summation
excitatory
postsynaptic
currents
have
been
proposed
to
contribute
signaling
at
tips
starbursts:
(1)
“morphological”
mechanism
which
electrotonic
propagation
synaptic
along
dendrite
sums
bipolar
cell
inputs
preferentially
stimulus
centrifugal
direction;
(2)
“space–time”
that
relies
on
differences
time-courses
proximal
distal
favor
motion.
To
explore
contributions
these
two
primate,
we
developed
realistic
computational
model
based
connectomic
reconstruction
distribution
its
sustained
transient
types.
Our
suggests
both
can
initiate
direction
selectivity
dendrites,
but
their
differ
depending
properties
stimulus.
Specifically,
morphological
dominates
when
small
objects
are
moving
high
velocities,
space–time
contributes
most
large
low
velocities.
iScience,
Journal Year:
2024,
Volume and Issue:
27(2), P. 108846 - 108846
Published: Jan. 9, 2024
Visual
processing
depends
on
sensitive
and
balanced
synaptic
neurotransmission.
Extracellular
matrix
proteins
in
the
environment
of
cells
are
key
modulators
synaptogenesis
plasticity.
In
present
study,
we
provide
evidence
that
combined
loss
four
extracellular
components,
brevican,
neurocan,
tenascin-C,
tenascin-R,
quadruple
knockout
mice
leads
to
severe
retinal
dysfunction
diminished
visual
motion
Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(36)
Published: Aug. 27, 2024
The
neural
pathways
that
start
human
color
vision
begin
in
the
complex
synaptic
network
of
foveal
retina
where
signals
originating
long
(L),
middle
(M),
and
short
(S)
wavelength-sensitive
cone
photoreceptor
types
are
compared
through
antagonistic
interactions,
referred
to
as
opponency.
In
nonhuman
primates,
two
opponent
well
established:
an
L
vs.
M
circuit
linked
midget
ganglion
cell
type,
often
called
red-green
pathway,
S
+
small
bistratified
blue-yellow
pathway.
These
have
been
taken
correspond
cardinal
directions
a
trichromatic
space,
providing
parallel
inputs
higher-level
processing.
Yet
linking
opponency
primate
mechanisms
has
proven
particularly
difficult.
Here,
we
apply
connectomic
reconstruction
trace
excitatory
outputs
from
S-ON
(or
“blue-cone”)
bipolar
additional
types:
large
subpopulation
ON-midget
cells,
whose
connections
suggest
significant
unique
role
vision.
postsynaptic
both
cells
thus
define
merge
circuits,
with
potential
for
at
first
stage
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.
Journal of Neuroscience,
Journal Year:
2023,
Volume and Issue:
44(10), P. e0910232023 - e0910232023
Published: Nov. 13, 2023
Classic
ON-OFF
direction-selective
ganglion
cells
(DSGCs)
that
encode
the
four
cardinal
directions
were
recently
shown
to
also
be
orientation-selective.
To
clarify
mechanisms
underlying
orientation
selectivity,
we
employed
a
variety
of
electrophysiological,
optogenetic,
and
gene
knock-out
strategies
test
relative
contributions
glutamate,
GABA,
acetylcholine
(ACh)
input
are
known
drive
DSGCs,
in
male
female
mouse
retinas.
Extracellular
spike
recordings
revealed
DSGCs
respond
preferentially
either
vertical
or
horizontal
bars,
those
perpendicular
their
preferred-null
motion
axes.
By
contrast,
glutamate
all
DSGC
types
measured
using
whole-cell
patch-clamp
techniques
was
found
tuned
along
axis.
Tuned
glutamatergic
excitation
heavily
reliant
on
type
5A
bipolar
cells,
which
appear
electrically
coupled
via
connexin
36
containing
gap
junctions
vertically
oriented
processes
wide-field
amacrine
cells.
Vertically
inputs
transformed
by
GABAergic/cholinergic
"starburst"
(SACs),
critical
components
circuit,
into
distinct
patterns
inhibition
excitation.
Feed-forward
SAC
appears
"veto"
preferred
dorsal/ventral
(but
not
nasal/temporal)
coding
"flipping"
tuning
90°
accounts
for
apparent
mismatch
between
DSGC's
spiking
response.
Together,
these
results
reveal
how
two
synaptic
motifs
interact
generate
complex
feature
shedding
light
intricate
circuitry
underlies
visual
processing
retina.