Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(47)
Published: Nov. 14, 2024
Imaging
methods
that
span
both
functional
measures
in
living
tissue
and
anatomical
fixed
have
played
critical
roles
advancing
our
understanding
of
the
brain.
However,
making
direct
comparisons
between
different
imaging
modalities,
particularly
spanning
tissue,
has
remained
challenging.
For
example,
comparing
brain-wide
neural
dynamics
across
experiments
aligning
such
data
to
resources,
as
gene
expression
patterns
or
connectomes,
requires
precise
alignment
a
common
set
coordinates.
reaching
this
goal
is
difficult
because
registering
vivo
ex
reference
atlases
accommodating
differences
modality,
microscope
specification,
sample
preparation.
We
overcome
these
challenges
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 18, 2024
ABSTRACT
Intestinal
mucin
acts
as
a
barrier
protecting
the
infant
gut
wall
against
diseases
such
colitis
and
rotavirus.
In
vitro
experiments
have
shown
that
microbiota
of
breastfed
infants
consumes
less
than
non-breastfed
infants,
but
mechanisms
are
incompletely
understood.
The
main
difference
between
human
milk
most
formulas
is
presence
oligosaccharides
(HMOs)
in
milk.
We
hypothesize
HMOs
protect
by
stimulating
non-mucin
consuming
bacteria.
To
understand
un-derlying
we
developed
computational
model
describes
metabolism
ecology
microbiota.
Model
simulations
suggest
extracellular
digestion
HMO
2’-fucosyllactose
mucin-consumer
Bifidobacterium
bifidum
may
make
this
species
vulnerable
to
competitors.
products
become
‘public
goods’
can
be
consumed
competing
Bacteroides
vulgatus
instead.
longum
,
which
does
not
consume
or
produce
public
goods,
then
dominant,
despite
growing
efficiently
on
monocultures
B.
.
conclusion,
our
that,
through
complex
ecological
interactions,
help
lower
consumption
consumer
at
expense
Techniques
that
enable
precise
manipulations
of
subsets
neurons
in
the
fly
central
nervous
system
(CNS)
have
greatly
facilitated
our
understanding
neural
basis
behavior.
Split-GAL4
driver
lines
allow
specific
targeting
cell
types
Drosophila
melanogaster
and
other
species.
We
describe
here
a
collection
3060
range
adult
CNS
1373
characterized
third-instar
larvae.
These
tools
functional,
transcriptomic,
proteomic
studies
based
on
anatomical
targeting.
NeuronBridge
search
relate
light
microscopy
images
these
split-GAL4
to
connectomes
reconstructed
from
electron
images.
The
collections
are
result
screening
over
77,000
split
hemidriver
combinations.
Previously
published
new
included,
all
validated
for
expression
curated
optimal
cell-type
specificity
across
diverse
types.
In
addition
stocks
well-characterized
lines,
we
make
available
300,000
3D
lines.
Techniques
that
enable
precise
manipulations
of
subsets
neurons
in
the
fly
central
nervous
system
have
greatly
facilitated
our
understanding
neural
basis
behavior.
Split-GAL4
driver
lines
allow
specific
targeting
cell
types
Drosophila
melanogaster
and
other
species.
We
describe
here
a
collection
3060
range
adult
1373
characterized
third-instar
larvae.
These
tools
functional,
transcriptomic,
proteomic
studies
based
on
anatomical
targeting.
NeuronBridge
search
relate
light
microscopy
images
these
split-GAL4
to
connectomes
reconstructed
from
electron
images.
The
collections
are
result
screening
over
77,000
split
hemidriver
combinations.
In
addition
stocks
for
well-characterized
lines,
we
make
available
300,000
new
3D
lines.
Proceedings of the National Academy of Sciences,
Journal Year:
2024,
Volume and Issue:
121(47)
Published: Nov. 14, 2024
Imaging
methods
that
span
both
functional
measures
in
living
tissue
and
anatomical
fixed
have
played
critical
roles
advancing
our
understanding
of
the
brain.
However,
making
direct
comparisons
between
different
imaging
modalities,
particularly
spanning
tissue,
has
remained
challenging.
For
example,
comparing
brain-wide
neural
dynamics
across
experiments
aligning
such
data
to
resources,
as
gene
expression
patterns
or
connectomes,
requires
precise
alignment
a
common
set
coordinates.
reaching
this
goal
is
difficult
because
registering
vivo
ex
reference
atlases
accommodating
differences
modality,
microscope
specification,
sample
preparation.
We
overcome
these
challenges