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
BCs
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
(DS)
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
DS
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
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
mechanisms
required
explain
SAC
function.
Our
provides
new
insights
complex
underlying
highlights
potential
contribution
computation
SACs.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: March 1, 2024
Abstract
How
sensory
systems
extract
salient
features
from
natural
environments
and
organize
them
across
neural
pathways
is
unclear.
Combining
single-cell
population
two-photon
calcium
imaging
in
mice,
we
discover
that
retinal
ON
bipolar
cells
(second-order
neurons
of
the
visual
system)
are
divided
into
two
blocks
four
types.
The
distribute
temporal
spatial
information
encoding,
respectively.
cell
axons
co-stratify
within
each
block,
but
separate
laminarly
between
(upper
block:
diverse
temporal,
uniform
tuning;
lower
spatial,
tuning).
similarly
artificial
naturalistic
stimuli.
In
addition,
they
differ
sensitivity
to
coherent
motion
movies.
Motion
distributed
upper
blocks,
multiplexed
with
contrast,
independent
scenes.
Comparing
responses
different
boutons
same
arbor,
find
all
types
function
as
computational
units.
Thus,
our
results
provide
insights
feature
extraction
stimuli
reveal
how
structural
functional
organization
cooperate
generate
parallel
for
mammalian
retina.
Visual
information
processing
is
sculpted
by
a
diverse
group
of
inhibitory
interneurons
in
the
retina
called
amacrine
cells.
Yet,
for
most
>60
cell
types,
molecular
identities
and
specialized
functional
attributes
remain
elusive.
Here,
we
developed
an
intersectional
genetic
strategy
to
target
wide-field
cells
(WACs)
mouse
that
co-express
transcription
factor
Bhlhe22
Kappa
Opioid
Receptor
(KOR;
B/K
WACs).
WACs
feature
straight,
unbranched
dendrites
spanning
over
0.5
mm
(∼15°
visual
angle)
produce
non-spiking
responses
either
light
increments
or
decrements.
Two-photon
dendritic
population
imaging
reveals
Ca
2+
signals
tuned
physical
orientations
WAC
dendrites,
signifying
robust
structure-function
alignment.
establish
divergent
connections
with
multiple
retinal
neurons,
including
unexpected
non-orientation-tuned
ganglion
bipolar
Our
work
sets
stage
future
comprehensive
investigations
enigmatic
neurons:
WACs.
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.
Annual Review of Vision Science,
Journal Year:
2024,
Volume and Issue:
10(1), P. 263 - 291
Published: Sept. 15, 2024
The
retina
is
an
ideal
model
for
understanding
the
fundamental
rules
how
neural
networks
are
constructed.
compact
of
perform
all
initial
processing
visual
information
before
transmission
to
higher
centers
in
brain.
field
retinal
connectomics
uses
high-resolution
electron
microscopy
datasets
map
intricate
organization
these
and
further
our
computations
performed
by
revealing
topologies
allowable
behind
computations.
In
this
article,
we
review
some
notable
advances
that
has
provided
specific
cells
their
connectivities
within
retina,
as
well
shaped
development
break
down
disease.
Using
anatomical
maps
inform
modeling
been,
will
continue
be,
instrumental
processes
signals.
Visual
information
processing
is
sculpted
by
a
diverse
group
of
inhibitory
interneurons
in
the
retina
called
amacrine
cells.
Yet,
for
most
>60
cell
types,
molecular
identities
and
specialized
functional
attributes
remain
elusive.
Here,
we
developed
an
intersectional
genetic
strategy
to
target
wide-field
cells
(WACs)
mouse
that
co-express
transcription
factor
Bhlhe22
Kappa
Opioid
Receptor
(KOR;
B/K
WACs).
WACs
feature
straight,
unbranched
dendrites
spanning
over
0.5
mm
(∼15°
visual
angle)
produce
non-spiking
responses
either
light
increments
or
decrements.
Two-photon
dendritic
population
imaging
reveals
Ca
2+
signals
tuned
physical
orientations
WAC
dendrites,
signifying
robust
structure-function
alignment.
establish
divergent
connections
with
multiple
retinal
neurons,
including
unexpected
non-orientation-tuned
ganglion
bipolar
Our
work
sets
stage
future
comprehensive
investigations
enigmatic
neurons:
WACs.
Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(49)
Published: Nov. 27, 2024
Orientation
is
one
of
the
most
salient
features
in
visual
scenes.
Neurons
at
multiple
levels
system
detect
orientation,
but
many
cases,
underlying
biophysical
mechanisms
remain
unresolved.
Here,
we
studied
for
orientation
detection
earliest
stage
system,
B/K
wide-field
amacrine
cells
(B/K
WACs),
a
group
giant,
nonspiking
interneurons
mouse
retina
that
coexpress
Bhlhe22
(B)
and
Kappa
Opioid
Receptor
(K).
WACs
exhibit
orientation-tuned
calcium
signals
along
their
long,
straight,
unbranching
dendrites,
which
contain
both
synaptic
inputs
outputs.
Simultaneous
dendritic
imaging
somatic
voltage
recordings
reveal
individual
dendrites
are
electrotonically
isolated,
exhibiting
spatially
confined
yet
extended
receptive
field
dendrite,
term
“compartmentalized
pooling.”
Further,
WAC
dendrite
exhibits
center-surround
antagonism.
Phenomenological
models
demonstrate
compartmentalized
pooling
generates
selectivity,
antagonism
shapes
band-pass
spatial
frequency
tuning.
At
microcircuit
level,
receive
excitation
driven
by
contrast
polarity
(e.g.,
“ON”)
glycinergic
inhibition
opposite
“OFF”).
However,
this
“crossover”
not
essential
generating
selectivity.
A
minimal
model
reproduced
from
feedforward
excitatory
combined
with
substantial
increase
specific
membrane
resistance
between
compartments.
Collectively,
our
results
mechanism
selectivity
WACs,
enriching
understanding
diverse
strategies
employed
throughout
to
orientation.
Frontiers in Ophthalmology,
Journal Year:
2023,
Volume and Issue:
3
Published: April 20, 2023
The
retinal
neural
circuit
is
intricately
wired
for
efficient
processing
of
visual
signals.
This
well-supported
by
the
specialized
connections
between
neurons
at
both
functional
and
ultrastructural
levels.
Through
3D
electron
microscopic
(EM)
reconstructions
circuits
we
have
learnt
much
about
specificities
within
layers
including
new
insights
into
how
establish
perform
sophisticated
computations.
mini-review
will
summarize
circuitry
provide
details
novel
EM
connectomics
has
brought
our
understanding
circuitry.
We
also
discuss
unresolved
questions
that
can
be
addressed
in
future.