In vivo autofluorescence lifetime imaging of the Drosophila brain captures metabolic shifts associated with memory formation
Опубликована: Март 31, 2025
Neuronal
energy
regulation
is
increasingly
recognized
as
a
critical
factor
underlying
brain
functions
and
their
pathological
alterations,
yet
the
metabolic
dynamics
that
accompany
cognitive
processes
remain
poorly
understood.
As
label-free
minimally
invasive
technique,
fluorescence
lifetime
imaging
(FLIM)
of
coenzymes
NADH
NADPH
(collectively
referred
to
NAD(P)H)
offers
possibility
resolve
cellular
profiles
with
high
spatial
precision.
However,
NAD(P)H
FLIM’s
capacity
detect
subtle
changes
in
neuronal
metabolism
associated
cognition
has
not
been
demonstrated.
In
this
study,
we
applied
FLIM
map
Drosophila
neurons
vivo
across
multiple
scales,
focusing
on
primary
centers
for
associative
memory:
mushroom
bodies
(MBs).
At
broad
scale,
obtained
an
overview
signatures
main
tissue
identified
marked
difference
between
neuropil
cortex
areas.
finer
our
findings
revealed
notable
heterogeneity
basal
distinct
MB
neuron
subtypes.
Measurements
performed
after
olfactory
learning
also
uncovered
subtype-specific
shift
memory
formation,
demonstrating
utility
detecting
physiology-driven
linked
function.
These
results
establish
promising
framework
studying
cerebral
vivo.
Язык: Английский
In vivo autofluorescence lifetime imaging of the Drosophila brain captures metabolic shifts associated with memory formation
Опубликована: Март 31, 2025
Neuronal
energy
regulation
is
increasingly
recognized
as
a
critical
factor
underlying
brain
functions
and
their
pathological
alterations,
yet
the
metabolic
dynamics
that
accompany
cognitive
processes
remain
poorly
understood.
As
label-free
minimally
invasive
technique,
fluorescence
lifetime
imaging
(FLIM)
of
coenzymes
NADH
NADPH
(collectively
referred
to
NAD(P)H)
offers
possibility
resolve
cellular
profiles
with
high
spatial
precision.
However,
NAD(P)H
FLIM’s
capacity
detect
subtle
changes
in
neuronal
metabolism
associated
cognition
has
not
been
demonstrated.
In
this
study,
we
applied
FLIM
map
Drosophila
neurons
vivo
across
multiple
scales,
focusing
on
primary
centers
for
associative
memory:
mushroom
bodies
(MBs).
At
broad
scale,
obtained
an
overview
signatures
main
tissue
identified
marked
difference
between
neuropil
cortex
areas.
finer
our
findings
revealed
notable
heterogeneity
basal
distinct
MB
neuron
subtypes.
Measurements
performed
after
olfactory
learning
also
uncovered
subtype-specific
shift
memory
formation,
demonstrating
utility
detecting
physiology-driven
linked
function.
These
results
establish
promising
framework
studying
cerebral
vivo.
Язык: Английский
Diverting glial glycolytic flux towards neurons is a memory-relevant role of Drosophila CRH-like signalling
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Дек. 2, 2024
Abstract
An
essential
role
of
glial
cells
is
to
comply
with
the
large
and
fluctuating
energy
needs
neurons.
Metabolic
adaptation
integral
acute
stress
response,
suggesting
that
could
be
major,
yet
overlooked,
targets
hormones.
Here
we
show
Dh44
neuropeptide,
Drosophila
homologue
mammalian
corticotropin-releasing
hormone
(CRH),
acts
as
an
experience-dependent
metabolic
switch
for
glycolytic
output
in
glia.
released
by
dopamine
neurons
limits
fatty
acid
synthesis
build-up
lipid
stores.
Although
basally
active,
this
hormonal
axis
acutely
stimulated
following
learning
a
danger-predictive
cue.
This
results
transient
suppression
anabolic
use
pyruvate,
sparing
it
memory-relevant
supply
Diverting
pyruvate
destination
may
dampen
need
upregulate
glycolysis
response
increased
neuronal
demand.
beneficial
efficiency
memory
formation,
mechanism
reveals
ongoing
competition
between
fuelling
anabolism.
Язык: Английский