Frontiers in Neuroinformatics,
Journal Year:
2019,
Volume and Issue:
13
Published: May 7, 2019
Our
knowledge
of
the
brain
has
evolved
over
millennia
in
philosophical,
experimental
and
theoretical
phases.
We
suggest
that
next
phase
is
simulation
neuroscience.
The
main
drivers
neuroscience
are
big
data
generated
at
multiple
levels
organization
need
to
integrate
these
trace
causal
chain
interactions
within
across
all
levels.
Simulation
currently
only
methodology
for
systematically
approaching
multiscale
brain.
In
this
review,
we
attempt
reconstruct
deep
historical
paths
leading
neuroscience,
from
first
observations
nerve
cell
modern
efforts
digitally
simulate
Neuroscience
began
with
identification
neuron
as
fundamental
unit
structure
function
towards
understanding
role
each
type
brain,
how
cells
connected
other,
seemingly
infinite
networks
they
form
give
rise
vast
diversity
functions.
Neuronal
mapping
evolving
subjective
descriptions
types
objective
classes,
subclasses
types.
Connectivity
loose
topographic
maps
between
regions
dense
anatomical
physiological
connections
individual
genetically
distinct
neurons.
Functional
psychological
behavioral
stereotypes
a
map
behaviors
emerging
structural
functional
connectomes.
show
industrialization
resulting
large
disconnected
datasets
generating
demand
integrative
scale
neuronal
connectivity
driving
digital
atlasing
reconstruction
piece
together
organization,
complexity
molecules,
neurons,
microcircuits
understand
Journal of Neuroscience,
Journal Year:
2020,
Volume and Issue:
40(27), P. 5177 - 5195
Published: May 26, 2020
Amacrine
cells
(ACs)
are
a
diverse
class
of
interneurons
that
modulate
input
from
photoreceptors
to
retinal
ganglion
(RGCs),
rendering
each
RGC
type
selectively
sensitive
particular
visual
features,
which
then
relayed
the
brain.
While
many
AC
types
have
been
identified
morphologically
and
physiologically,
they
not
comprehensively
classified
or
molecularly
characterized.
We
used
high-throughput
single-cell
RNA
sequencing
profile
>32,000
ACs
mice
both
sexes
applied
computational
methods
identify
63
types.
molecular
markers
for
them
characterize
morphology
multiple
show
include
nearly
all
previously
known
as
well
had
described.
Consistent
with
previous
studies,
most
expressed
canonical
inhibitory
neurotransmitters
GABA
glycine,
but
several
neither
both.
In
addition,
one
more
neuropeptides,
two
glutamatergic
markers.
also
explored
transcriptomic
relationships
among
transcription
factors
by
individual
closely
related
Noteworthy
these
were
Meis2Tcf4,
GABAergic
glycinergic
types,
respectively.
Together,
results
provide
foundation
developmental
functional
studies
ACs,
means
genetically
accessing
them.
Along
molecular,
physiological,
morphologic
analyses,
establish
existence
at
least
130
neuronal
140
cell
in
mouse
retina.
SIGNIFICANCE
STATEMENT
The
retina
is
leading
model
analyzing
development,
structure,
function,
pathology
neural
circuits.
A
complete
atlas
provides
an
important
studies.
heterogeneous
interneurons,
amacrine
cells,
identifying
distinct
includes
novel
evidence
use
groups
Combining
those
obtained
previously,
we
proposed
contains
∼130
therefore
comparable
complexity
other
regions
In
the
mouse
retina,
three
different
types
of
photoreceptors
provide
input
to
14
bipolar
cell
(BC)
types.
Classically,
most
BC
are
thought
contact
all
cones
within
their
dendritic
field;
ON-BCs
would
exclusively
via
so-called
invaginating
synapses,
while
OFF-BCs
form
basal
synapses.
By
mining
publically
available
electron
microscopy
data,
we
discovered
interesting
violations
these
rules
outer
retinal
connectivity:
ON-BC
type
X
contacted
only
~20%
in
its
field
and
made
mostly
atypical
non-invaginating
contacts.
Types
5T,
5O
8
also
fewer
than
expected.
addition,
found
that
rod
BCs
received
from
cones,
providing
anatomical
evidence
cone
pathways
interconnected
both
directions.
This
suggests
organization
plexiform
layer
is
more
complex
classically
thought.
Annual Review of Neuroscience,
Journal Year:
2017,
Volume and Issue:
40(1), P. 211 - 230
Published: April 18, 2017
Images
projected
onto
the
retina
of
an
animal
eye
are
rarely
still.
Instead,
they
usually
contain
motion
signals
originating
either
from
moving
objects
or
retinal
slip
caused
by
self-motion.
Accordingly,
tell
in
which
direction
a
predator,
prey,
itself
is
moving.
At
neural
level,
visual
detection
has
been
proposed
to
extract
directional
information
delay-and-compare
mechanism,
representing
classic
example
computation.
Neurons
responding
selectively
one
but
not
other
have
identified
many
systems,
most
prominently
mammalian
and
fly
optic
lobe.
Technological
advances
now
allowed
researchers
characterize
these
neurons'
upstream
circuits
exquisite
detail.
Focusing
on
circuits,
we
review
compare
recent
progress
understanding
mechanisms
that
generate
selectivity
early
system
mammals
flies.