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.
Cell Reports,
Journal Year:
2022,
Volume and Issue:
40(2), P. 111040 - 111040
Published: July 1, 2022
Classification
and
characterization
of
neuronal
types
are
critical
for
understanding
their
function
dysfunction.
Neuronal
classification
schemes
typically
rely
on
measurements
electrophysiological,
morphological,
molecular
features,
but
aligning
such
datasets
has
been
challenging.
Here,
we
present
a
unified
mouse
retinal
ganglion
cells
(RGCs),
the
sole
output
neurons.
We
use
visually
evoked
responses
to
classify
1,859
RGCs
into
42
types.
also
obtain
morphological
or
transcriptomic
data
from
subsets
these
align
functional
publicly
available
datasets.
create
an
online
database
that
allows
users
browse
download
light
using
machine
learning
algorithm.
This
work
provides
resource
studies
RGCs,
upstream
circuits
in
retina,
projections
brain,
establishes
framework
future
efforts
open
distribution.
Neuron-glia
interactions
play
a
critical
role
in
the
maturation
of
neural
circuits;
however,
little
is
known
about
pathways
that
mediate
their
communication
developing
CNS.
We
investigated
neuron-glia
signaling
retina,
where
we
demonstrate
retinal
waves
reliably
induce
calcium
transients
Müller
glial
cells
(MCs).
During
cholinergic
waves,
MC
were
blocked
by
muscarinic
acetylcholine
receptor
antagonists,
whereas
during
glutamatergic
inhibited
ionotropic
glutamate
indicating
responsiveness
MCs
changes
to
match
neurotransmitter
used
support
waves.
Using
an
optical
sensor
show
decline
caused
reduction
amount
reaching
MCs.
Together,
these
studies
indicate
neurons
and
exhibit
correlated
activity
period
enabled
spillover
from
synapses.
Neuron,
Journal Year:
2017,
Volume and Issue:
93(4), P. 767 - 776.e6
Published: Feb. 1, 2017
The
thalamus
receives
sensory
input
from
different
circuits
in
the
periphery.
How
these
channels
are
integrated
at
level
of
single
thalamic
cells
is
not
well
understood.
We
performed
targeted
single-cell-initiated
transsynaptic
tracing
to
label
retinal
ganglion
that
provide
individual
principal
mouse
lateral
geniculate
nucleus
(LGN).
identified
three
modes
integration
by
LGN
cells.
In
first,
1-5
mostly
same
type
converged
one
eye,
indicating
a
relay
mode.
second,
6-36
types
revealing
combination
third,
up
91
both
eyes,
binocular
mode
which
functionally
specialized
ipsilateral
inputs
joined
broadly
distributed
contralateral
inputs.
Thus,
employs
least
visual
integration,
each
exhibiting
degrees
specialization.
Journal of Neuroscience,
Journal Year:
2016,
Volume and Issue:
36(40), P. 10404 - 10415
Published: Oct. 5, 2016
Excitatory
amino
acid
transporters
(EAATs)
are
abundantly
expressed
by
astrocytes,
rapidly
remove
glutamate
from
the
extracellular
environment,
and
restrict
temporal
spatial
extent
of
signaling.
Studies
probing
EAAT
function
suggest
that
their
capacity
to
is
large
does
not
saturate,
even
with
substantial
challenges.
In
contrast,
we
report
neuronal
activity
reversibly
modulates
EAAT-dependent
transport.
To
date,
no
physiological
manipulation
has
shown
changes
in
functional
uptake
a
nonpathological
state.
Using
iGluSnFr-based
imaging
electrophysiology
adult
mouse
cortex,
show
slowed
up
threefold
following
bursts
activity.
The
slowing
depends
on
frequency
duration
presynaptic
but
independent
amount
released.
modulation
brief,
returning
normal
within
50
ms
after
stimulation
ceases.
Interestingly,
specific
activated
synapses,
domain
an
individual
astrocyte.
Activity-induced
uptake,
increased
persistence
space,
reflected
decay
times
NR2A-mediated
NMDA
currents.
These
results
astrocytic
clearance
temporally
spatially
manner
≥30
Hz
these
affect
response
released
glutamate.
This
suggests
previously
unreported
form
neuron–astrocyte
interaction.
SIGNIFICANCE
STATEMENT
We
first
fast,
astrocyte
kinetics.
cerebral
cortex
increases
space
its
astrocytes.
Because
abundant
expression,
been
thought
have
invariant
While
multiple
studies
experimental
manipulations
resulting
altered
our
findings
dynamic
fast
time-scale.
shows
rapid
plasticity
clearance,
which
locally
synaptic
signaling
cortex.
As
fundamental
essential
mechanism
for
neurotransmission,
this
work
implications
extrasynaptic
receptor
activation,
plasticity.
Neurophotonics,
Journal Year:
2014,
Volume and Issue:
1(2), P. 025008 - 025008
Published: Oct. 17, 2014
A
major
goal
of
the
BRAIN
Initiative
is
development
technologies
to
monitor
neuronal
network
activity
during
active
information
processing.
Toward
this
goal,
genetically
encoded
calcium
indicator
proteins
have
become
widely
used
for
reporting
in
preparations
ranging
from
invertebrates
awake
mammals.
However,
slow
response
times,
narrow
sensitivity
range
Ca2+
and
some
cases,
poor
signal-to-noise
ratio
still
limit
their
usefulness.
Here,
we
review
recent
improvements
field
neural
activity-sensitive
probe
design
with
a
focus
on
GCaMP
family
proteins.
In
context,
present
our
newly
developed
Fast-GCaMPs,
which
up
4-fold
accelerated
off-responses
compared
next-fastest
GCaMP,
GCaMP6f.
Fast-GCaMPs
were
designed
by
destabilizing
association
hydrophobic
pocket
calcium-bound
calmodulin
RS20
binding
domain,
an
intramolecular
interaction
that
protects
green
fluorescent
protein
chromophore.
Fast-GCaMP6f-RS06
Fast-GCaMP6f-RS09
rapid
stopped-flow
fluorimetry,
neocortical
brain
slices,
intact
cerebellum
vivo.
Fast-GCaMP6f
variants
should
be
useful
tracking
action
potentials
closely
spaced
time,
following
fast-changing
compartments,
such
as
axons
dendrites.
Finally,
discuss
strategies
may
allow
wider
firing
rates
improve
spike
detection.
Nature Communications,
Journal Year:
2017,
Volume and Issue:
8(1)
Published: July 20, 2017
Neurons
in
sensory
systems
often
pool
inputs
over
arrays
of
presynaptic
cells,
giving
rise
to
functional
subunits
inside
a
neuron's
receptive
field.
The
organization
these
provides
signature
the
connectivity
and
determines
how
neuron
integrates
stimuli.
Here
we
introduce
method
spike-triggered
non-negative
matrix
factorization
for
detecting
layout
within
only
requires
spiking
responses
under
finely
structured
stimulation
is
therefore
applicable
large
populations
simultaneously
recorded
neurons.
Applied
recordings
from
ganglion
cells
salamander
retina,
retrieves
fields
bipolar
as
verified
by
simultaneous
cell
recordings.
identified
subunit
layouts
allow
improved
predictions
natural
stimuli
reveal
shared
input
into
distinct
types
cells.How
information
knowledge
about
its
connections.
authors
report
new
using
identify
onto
retinal
predict
their