bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Авг. 19, 2024
Abstract
Capturing
the
intricate
dynamics
of
neural
activity
in
freely
behaving
animals
is
essential
for
understanding
mechanisms
underpinning
specific
behaviors.
Miniaturized
microscopy
enables
investigators
to
track
population
at
cellular
level,
but
field
view
(FOV)
these
microscopes
have
been
limited
and
does
not
allow
multiple-brain
region
imaging.
To
fill
this
technological
gap,
we
developed
eXtra
Large
field-of-view
Miniscope
(MiniXL),
a
3.5g
lightweight
miniaturized
microscope
with
an
FOV
measuring
3.5
mm
diameter
electrically
adjustable
working
distance
1.9
±
200
μm.
We
demonstrated
capability
MiniXL
recording
large
neuronal
both
subcortical
area
(hippocampal
dorsal
CA1)
deep
brain
regions
(medial
prefrontal
cortex,
mPFC
nucleus
accumbens,
NAc).
The
allows
simultaneous
imaging
multiple
such
as
bilateral
mPFCs
or
NAc
during
complex
social
behavior
tracking
cells
across
sessions.
As
all
UCLA
ecosystem,
fully
open-source
will
be
shared
neuroscience
community
lower
barriers
adoption
technology.
Cell,
Год журнала:
2022,
Номер
185(7), С. 1240 - 1256.e30
Опубликована: Март 1, 2022
We
developed
a
miniaturized
two-photon
microscope
(MINI2P)
for
fast,
high-resolution,
multiplane
calcium
imaging
of
over
1,000
neurons
at
time
in
freely
moving
mice.
With
weight
below
3
g
and
highly
flexible
connection
cable,
MINI2P
allowed
stable
with
no
impediment
behavior
variety
assays
compared
to
untethered,
unimplanted
animals.
The
improved
cell
yield
was
achieved
through
optical
system
design
featuring
an
enlarged
field
view
(FOV)
microtunable
lens
increased
z-scanning
range
speed
that
allows
fast
multiple
interleaved
planes,
as
well
3D
functional
imaging.
Successive
across
multiple,
adjacent
FOVs
enabled
recordings
from
more
than
10,000
the
same
animal.
Large-scale
proof-of-principle
data
were
obtained
populations
visual
cortex,
medial
entorhinal
hippocampus,
revealing
spatial
tuning
cells
all
areas.
Optica,
Год журнала:
2021,
Номер
8(5), С. 614 - 614
Опубликована: Март 18, 2021
Volumetric
interrogation
of
the
organization
and
processes
intracellular
organelles
molecules
in
cellular
systems
with
a
high
spatiotemporal
resolution
is
essential
for
understanding
cell
physiology,
development,
pathology.
Here,
we
report
high-resolution
Fourier
light-field
microscopy
(HR-FLFM)
fast
volumetric
live-cell
imaging.
HR-FLFM
transforms
conventional
enables
exploration
less
accessible
spatiotemporal-limiting
regimes
single-cell
studies.
The
results
present
near-diffraction-limited
all
three
dimensions,
five-fold
extended
focal
depth
to
several
micrometers,
scanning-free
volume
acquisition
time
up
milliseconds.
system
demonstrates
instrumentation
accessibility,
low
photo
damage
continuous
observation,
compatibility
general
assays.
We
anticipate
offer
promising
methodological
pathway
investigating
wide
range
functions
exquisite
contextual
details.
Nature Photonics,
Год журнала:
2024,
Номер
18(7), С. 721 - 730
Опубликована: Апрель 17, 2024
Abstract
Benefitting
from
the
advantages
of
high
imaging
throughput
and
low
cost,
wide-field
microscopy
has
become
indispensable
in
biomedical
studies.
However,
it
remains
challenging
to
record
biodynamics
with
a
large
field
view
spatiotemporal
resolution
due
limited
space–bandwidth
product.
Here
we
propose
random-access
(RA-WiFi)
mesoscopy
for
vivo
over
163.84
mm
2
area
spatial
~2.18
μm.
We
extend
beyond
nominal
value
objective
by
enlarging
object
distance,
which
leads
lower
angle,
followed
correction
optical
aberrations.
also
implement
scanning
structured
illumination,
enables
optical-sectioning
capability
contrast.
The
multi-plane
makes
technique
suitable
curved-surface
samples.
demonstrate
RA-WiFi
multi-modal
imaging,
including
bright-field,
dark-field
multi-colour
fluorescence
imaging.
Specifically,
apply
calcium
cortex-wide
neural
network
activities
awake
mice
vivo,
under
both
physiological
pathological
conditions.
show
its
unique
three-dimensional
random
access
irregular
regions
interest
via
biodynamic
mouse
spinal
cords
vivo.
As
compact,
low-cost
mesoscope
capability,
will
enable
broad
applications
study
biological
systems.
Light Science & Applications,
Год журнала:
2024,
Номер
13(1)
Опубликована: Июнь 26, 2024
Abstract
Ultrafast
3D
imaging
is
indispensable
for
visualizing
complex
and
dynamic
biological
processes.
Conventional
scanning-based
techniques
necessitate
an
inherent
trade-off
between
acquisition
speed
space-bandwidth
product
(SBP).
Emerging
single-shot
wide-field
offer
a
promising
alternative
but
are
bottlenecked
by
the
synchronous
readout
constraints
of
conventional
CMOS
systems,
thus
restricting
data
throughput
to
maintain
high
SBP
at
limited
frame
rates.
To
address
this,
we
introduce
EventLFM,
straightforward
cost-effective
system
that
overcomes
these
challenges
integrating
event
camera
with
Fourier
light
field
microscopy
(LFM),
state-of-the-art
technique.
The
operates
on
novel
asynchronous
architecture,
thereby
bypassing
rate
limitations
systems.
We
further
develop
simple
robust
event-driven
LFM
reconstruction
algorithm
can
reliably
reconstruct
dynamics
from
unique
spatiotemporal
measurements
captured
EventLFM.
Experimental
results
demonstrate
EventLFM
robustly
fast-moving
rapidly
blinking
fluorescent
samples
kHz
Furthermore,
highlight
EventLFM’s
capability
neuronal
signals
in
scattering
mouse
brain
tissues
tracking
GFP-labeled
neurons
freely
moving
C.
elegans
.
believe
combined
ultrafast
large
offered
may
open
up
new
possibilities
across
many
biomedical
applications.
Optica,
Год журнала:
2022,
Номер
9(9), С. 1009 - 1009
Опубликована: Авг. 3, 2022
Fluorescence
microscopy
is
essential
to
study
biological
structures
and
dynamics.
However,
existing
systems
suffer
from
a
tradeoff
between
field-of-view
(FOV),
resolution,
complexity,
thus
cannot
fulfill
the
emerging
need
of
miniaturized
platforms
providing
micron-scale
resolution
across
centimeter-scale
FOVs.
To
overcome
this
challenge,
we
developed
Computational
Miniature
Mesoscope
(CM$^2$)
that
exploits
computational
imaging
strategy
enable
single-shot
3D
high-resolution
wide
FOV
in
platform.
Here,
present
CM$^2$
V2
significantly
advances
both
hardware
computation.
We
complement
3$\times$3
microlens
array
with
new
hybrid
emission
filter
improves
contrast
by
5$\times$,
design
3D-printed
freeform
collimator
for
LED
illuminator
excitation
efficiency
3$\times$.
reconstruction
large
volume,
develop
an
accurate
efficient
linear
shift-variant
(LSV)
model
characterizes
spatially
varying
aberrations.
then
train
multi-module
deep
learning
model,
CM$^2$Net,
using
only
3D-LSV
simulator.
show
CM$^2$Net
generalizes
well
experiments
achieves
$\sim$7-mm
800-$\mu$m
depth,
provides
$\sim$6-$\mu$m
lateral
$\sim$25-$\mu$m
axial
resolution.
This
$\sim$8$\times$
better
localization
$\sim$1400$\times$
faster
speed
as
compared
previous
model-based
algorithm.
anticipate
simple
low-cost
miniature
system
will
be
impactful
many
large-scale
fluorescence
applications.
Neurophotonics
was
launched
in
2014
coinciding
with
the
launch
of
BRAIN
Initiative
focused
on
development
technologies
for
advancement
neuroscience.
For
last
seven
years,
Neurophotonics'
agenda
has
been
well
aligned
this
focus
neurotechnologies
featuring
new
optical
methods
and
tools
applicable
to
brain
studies.
While
2.0
is
pivoting
towards
applications
these
novel
quest
understand
brain,
article
we
review
an
extensive
diverse
toolkit
explore
function
that
have
emerged
from
related
large-scale
efforts
measurement
manipulation
structure
function.
Here,
neurophotonic
mostly
animal
A
companion
article,
scheduled
appear
later
year,
will
cover
diffuse
imaging
noninvasive
human
each
domain,
outline
current
state-of-the-art
respective
technologies,
identify
areas
where
innovation
needed
provide
outlook
future
directions.