Journal of Neuroscience,
Journal Year:
2016,
Volume and Issue:
37(3), P. 610 - 625
Published: Dec. 5, 2016
Retinal
ganglion
cells
(RGCs)
are
frequently
divided
into
functional
types
by
their
ability
to
extract
and
relay
specific
features
from
a
visual
scene,
such
as
the
capacity
discern
local
or
global
motion,
direction
of
stimulus
orientation,
contrast
uniformity,
presence
large
small
objects.
Here
we
introduce
three
previously
uncharacterized,
nondirection-selective
ON–OFF
RGC
that
represent
distinct
set
feature
detectors
in
mouse
retina.
The
high-definition
(HD)
RGCs
possess
receptive-field
centers
strong
surround
suppression.
They
respond
selectively
objects
sizes,
speeds,
motion.
We
present
comprehensive
morphological
characterization
HD
physiological
recordings
light
responses,
size
structure,
synaptic
mechanisms
also
explore
similarities
differences
between
well
characterized
with
comparably
receptive
field,
edge
detector,
response
moving
textures.
model
populations
each
type
study
how
they
differ
performance
tracking
object.
These
results,
besides
introducing
new
together
constitute
substantial
fraction
RGCs,
provide
insights
role
different
circuits
shaping
fields
establish
foundation
for
continued
suppression
neural
basis
motion
detection.
SIGNIFICANCE
STATEMENT
output
retina,
retinal
(RGCs),
diverse
group
∼40
neuron
often
assigned
“feature
detection”
profiles
based
on
aspects
scene
which
respond.
describe,
first
time,
substantially
augmenting
our
understanding
selectivity.
Experiments
modeling
show
while
these
“high-definition”
share
certain
properties,
have
tuning
size,
speed,
enabling
them
occupy
niches
space.
The
function
of
a
neural
circuit
is
shaped
by
the
computations
performed
its
interneurons,
which
in
many
cases
are
not
easily
accessible
to
experimental
investigation.
Here,
we
elucidate
transformation
visual
signals
flowing
from
input
output
primate
retina,
using
combination
large-scale
multi-electrode
recordings
an
identified
ganglion
cell
type,
stimulation
targeted
at
individual
cone
photoreceptors,
and
hierarchical
computational
model.
results
reveal
nonlinear
subunits
circuity
OFF
midget
cells,
subserve
high-resolution
vision.
model
explains
light
responses
variety
stimuli
more
accurately
than
linear
model,
including
cones
within
across
subunits.
recovered
components
consistent
with
known
anatomical
organization
bipolar
interneurons.
These
spatial
structure
encoding,
resolution
single
cells
scale
complete
circuits.
Reports on Progress in Physics,
Journal Year:
2016,
Volume and Issue:
79(9), P. 096701 - 096701
Published: Aug. 9, 2016
Retinal
prostheses
are
a
promising
means
for
restoring
sight
to
patients
blinded
by
the
gradual
atrophy
of
photoreceptors
due
retinal
degeneration.
They
designed
reintroduce
information
into
visual
system
electrically
stimulating
surviving
neurons
in
retina.
This
review
outlines
concepts
and
technologies
behind
two
major
approaches
prosthetics:
epiretinal
subretinal.
We
describe
how
responds
electrical
stimulation.
highlight
differences
between
direct
encoding
output
with
stimulation,
network-mediated
response
subretinal
summarize
results
pre-clinical
evaluation
prosthetic
functions
in-
ex
vivo,
as
well
outcomes
current
clinical
trials
various
implants.
also
briefly
alternative,
non-electronic,
restoration
blind,
conclude
suggesting
some
perspectives
future
advancement
field.
Retinal
circuits
detect
salient
features
of
the
visual
world
and
report
them
to
brain
through
spike
trains
retinal
ganglion
cells.
The
most
abundant
cell
type
in
mice,
so-called
W3
cell,
selectively
responds
movements
small
objects.
Where
how
object
motion
sensitivity
arises
retina
is
incompletely
understood.
In
this
study,
we
use
2-photon-guided
patch-clamp
recordings
characterize
responses
vesicular
glutamate
transporter
3
(VGluT3)-expressing
amacrine
cells
(ACs)
a
broad
set
stimuli.
We
find
that
these
ACs
are
sensitive
analyze
synaptic
mechanisms
underlying
computation.
Anatomical
circuit
reconstructions
suggest
VGluT3-expressing
form
glutamatergic
synapses
with
cells,
targeted
show
tuning
cells'
excitatory
input
matches
ACs'
responses.
Synaptic
excitation
diminished,
suppressed
mice
lacking
VGluT3.
Object
motion,
thus,
first
detected
by
ACs,
which
provide
feature-selective
Journal of Neuroscience,
Journal Year:
2016,
Volume and Issue:
37(3), P. 610 - 625
Published: Dec. 5, 2016
Retinal
ganglion
cells
(RGCs)
are
frequently
divided
into
functional
types
by
their
ability
to
extract
and
relay
specific
features
from
a
visual
scene,
such
as
the
capacity
discern
local
or
global
motion,
direction
of
stimulus
orientation,
contrast
uniformity,
presence
large
small
objects.
Here
we
introduce
three
previously
uncharacterized,
nondirection-selective
ON–OFF
RGC
that
represent
distinct
set
feature
detectors
in
mouse
retina.
The
high-definition
(HD)
RGCs
possess
receptive-field
centers
strong
surround
suppression.
They
respond
selectively
objects
sizes,
speeds,
motion.
We
present
comprehensive
morphological
characterization
HD
physiological
recordings
light
responses,
size
structure,
synaptic
mechanisms
also
explore
similarities
differences
between
well
characterized
with
comparably
receptive
field,
edge
detector,
response
moving
textures.
model
populations
each
type
study
how
they
differ
performance
tracking
object.
These
results,
besides
introducing
new
together
constitute
substantial
fraction
RGCs,
provide
insights
role
different
circuits
shaping
fields
establish
foundation
for
continued
suppression
neural
basis
motion
detection.
SIGNIFICANCE
STATEMENT
output
retina,
retinal
(RGCs),
diverse
group
∼40
neuron
often
assigned
“feature
detection”
profiles
based
on
aspects
scene
which
respond.
describe,
first
time,
substantially
augmenting
our
understanding
selectivity.
Experiments
modeling
show
while
these
“high-definition”
share
certain
properties,
have
tuning
size,
speed,
enabling
them
occupy
niches
space.