Frontiers in Neuroinformatics,
Journal Year:
2023,
Volume and Issue:
17
Published: Dec. 1, 2023
Characterizing
the
connectomic
and
morphological
diversity
of
thalamic
neurons
is
key
for
better
understanding
how
thalamus
relays
sensory
inputs
to
cortex.
The
recent
public
release
complete
single-neuron
reconstructions
enables
analysis
previously
inaccessible
connectivity
patterns
from
individual
neurons.
Here
we
focus
on
Ventral
Posteromedial
(VPM)
nucleus
characterize
full
257
VPM
neurons,
obtained
by
combining
data
MouseLight
Braintell
projects.
Neurons
were
clustered
according
their
most
dominantly
targeted
cortical
area
further
subdivided
jointly
areas.
We
a
2D
embedding
using
dissimilarity
between
all
pairs
axonal
trees.
curved
shape
allowed
us
1-dimensional
coordinate.
coordinate
values
aligned
both
with
progression
soma
position
along
dorsal-ventral
lateral-medial
axes
that
terminals
posterior-anterior
medial-lateral
axes,
as
well
an
increase
in
number
branching
points,
distance
width.
Taken
together,
have
developed
novel
workflow
linking
three
challenging
aspects
connectomics,
namely
topography,
higher
order
diversity,
test-case.
linked
unified
access
portal
contains
morphologies
integrated
flatmap
subcortical
visualization
tools.
resulting
processed
been
made
available
Python,
can
thus
be
used
modeling
experimentally
validating
new
hypotheses
thalamocortical
connectivity.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 12, 2025
Abstract
Lipid
membranes
are
key
to
the
nanoscale
compartmentalization
of
biological
systems,
but
fluorescent
visualization
them
in
intact
tissues,
with
precision,
is
challenging
do
high
labeling
density.
Here,
we
report
ultrastructural
membrane
expansion
microscopy
(umExM),
which
combines
an
innovative
label
and
optimized
protocol,
support
dense
tissues
for
visualization.
We
validate
signal-to-background
ratio,
uniformity
continuity,
umExM
brain
slices,
supports
imaging
proteins
at
a
resolution
~60
nm
on
confocal
microscope.
demonstrate
utility
segmentation
tracing
neuronal
processes,
such
as
axons,
mouse
tissue.
Combining
optical
fluctuation
imaging,
or
iterating
process,
yields
~35
pointing
towards
potential
electron
ordinary
light
microscopes.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 21, 2023
In
2015,
we
launched
the
mesoSPIM
initiative
(www.mesospim.org),
an
open-source
project
for
making
light-sheet
microscopy
of
large
cleared
tissues
more
accessible.
Meanwhile,
demand
imaging
larger
samples
at
higher
speed
and
resolution
has
increased,
requiring
major
improvements
in
capabilities
microscopy.
Here,
introduce
next-generation
("Benchtop")
with
significantly
increased
field
view,
improved
resolution,
throughput,
affordable
cost
simpler
assembly
compared
to
original
version.
We
developed
a
new
method
testing
objectives,
enabling
us
select
detection
objectives
optimal
large-sensor
sCMOS
cameras.
The
achieves
high
spatial
(1.5
μm
laterally,
3.3
axially)
across
entire
magnification
up
20x,
supports
sample
sizes
ranging
from
sub-mm
several
centimetres,
while
being
compatible
multiple
clearing
techniques.
microscope
serves
broad
range
applications
neuroscience,
developmental
biology,
even
physics.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(42)
Published: Oct. 16, 2024
The
mesoscope
has
emerged
as
a
powerful
imaging
tool
in
biomedical
research,
yet
its
high
cost
and
low
resolution
have
limited
broader
application.
Here,
we
introduce
the
Omni-Mesoscope,
high–spatial-temporal
multimodal
mesoscopic
platform
built
from
cost-efficient
off-the-shelf
components.
This
system
uniquely
merges
capabilities
of
label-free
quantitative
phase
microscopy
to
capture
live-cell
morphodynamics
across
thousands
cells
with
highly
multiplexed
fluorescence
for
comprehensive
molecular
characterization.
Omni-Mesoscope
offers
mesoscale
field
view
~5
square
millimeters
spatial
down
700
nanometers,
enabling
detailed
subcellular
features.
We
demonstrate
capability
delineating
characteristics
underlying
rare
morphodynamic
cellular
phenomena,
including
cancer
cell
responses
chemotherapy
emergence
polyploidy
drug-resistant
cells.
also
integrate
expansion
technique
enhance
three-dimensional
volumetric
super-resolution
thicker
tissues,
opening
avenues
biological
exploration
at
unprecedented
scales
resolutions.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Nov. 5, 2023
Expansion
microscopy
and
light
sheet
imaging
enable
fine-scale
resolution
of
intracellular
features
that
comprise
neural
circuits.
Most
current
techniques
visualize
sparsely
distributed
across
whole
brains
or
densely
within
individual
brain
regions.
Here,
we
dense
distributions
immunolabeled
proteins
early
visual
cortical
areas
in
adult
macaque
monkeys.
This
process
may
be
combined
with
multiphoton
magnetic
resonance
to
produce
multimodal
atlases
large,
gyrencephalic
brains.
Journal of Neuroscience,
Journal Year:
2023,
Volume and Issue:
43(45), P. 7587 - 7598
Published: Nov. 8, 2023
The
human
brain
represents
one
of
the
most
complex
biological
systems,
containing
billions
neurons
interconnected
through
trillions
synapses.
Inherent
to
is
a
biochemical
complexity
involving
ions,
signaling
molecules,
and
peptides
that
regulate
neuronal
activity
allow
for
short-
long-term
adaptations.
Large-scale
noninvasive
imaging
techniques,
such
as
fMRI
EEG,
have
highlighted
regions
involved
in
specific
functions
visualized
connections
between
different
areas.
A
major
shortcoming,
however,
need
more
information
on
cell
types
neurotransmitters
involved,
well
poor
spatial
temporal
resolution.
Recent
technologies
been
advanced
circuit
mapping
implemented
behaving
model
organisms
address
this.
Here,
we
highlight
strategies
targeting
subtypes,
identifying,
releasing
controlling
gene
expression,
monitoring
circuits
real-time
vivo
.
Combined,
these
approaches
us
establish
direct
causal
links
from
genes
molecules
systems
level
ultimately
cognitive
processes.
The Transmitter,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Jan. 1, 2023
By
bloating
brain
samples
and
imaging
them
with
a
powerful
microscope,
researchers
can
reconstruct
neurons
across
the
entire
mouse
brain,
according
to
new
preprint.The
technique
could
help
scientists
uncover
neural
circuits
responsible
for
complex
behaviors,
as
well
pathways
that
are
altered
in
neurological
conditions.Tracking
axons
understand
how
individual
areas
communicate
over
long
distances.But
tracing
their
path
through
is
tricky,
says
study
investigator
Adam
Glaser,
senior
scientist
at
Allen
Institute
Neural
Dynamics
Seattle,
Washington.Axons,
which
capable
of
spanning
be
less
than
micrometer
diameter,
so
mapping
route
requires
detailed
imaging,
he
says.One
existing
approach
involves
microscope
slices
off
an
ultra-thin
section
then
scans
it,
repeating
process
about
20,000
times
capture
brain.Scientists
blend
images
together
form
3D
reconstruction
neuronal
pathways.https://www.spectrumnews.org/wp-content/uploads/2023/07/1200-inside-Video-3.mp4
Illuminated
axons:The
tool
trace
all
24
hours.But
takes
several
days
therefore
more
prone
complications
-bubbles
forming
on
lens,
say
-than
faster
techniques,
Glaser
says.And
slicing
distort
edges
image,
making
it
"challenging
or
impossible"
stitch
back
together,