Orienting
behaviors
provide
a
continuous
stream
of
information
about
an
organism’s
sensory
experiences
and
plans.
Thus,
to
study
the
links
between
sensation
action,
it
is
useful
identify
neurons
in
brain
that
control
orienting
behaviors.
Here
we
describe
descending
Drosophila
predict
influence
orientation
(heading)
during
walking.
We
show
these
cells
have
specialized
functions:
whereas
one
cell
type
predicts
sustained
low-gain
steering,
other
transient
high-gain
steering.
These
latter
integrate
internally-directed
steering
signals
from
head
direction
system
with
stimulus-directed
multimodal
pathways.
The
inputs
are
organized
produce
“see-saw”
commands,
so
increasing
output
hemisphere
accompanied
by
decreasing
hemisphere.
Together,
our
results
internal
external
drives
integrated
motor
commands
different
timescales,
for
flexible
precise
space.
Current Biology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Highlights•The
descending
neuron
DNp03
in
Drosophila
responds
to
aversive
looming
stimuli•Its
spiking
activity
is
state
dependent
and
correlated
with
flight
saccades•DNp03
provides
input
other
neurons
involved
controlling
turns•Optogenetic
activation
of
can
initiate
free-flight
saccadesSummaryApproaching
threats
are
perceived
through
visual
looming,
a
rapid
expansion
an
image
on
the
retina.
Visual
triggers
defensive
responses
such
as
freezing,
flight,
turning,
or
take-off
wide
variety
organisms,
from
mice
fish
insects.1,2,3,4
In
response
flies
perform
evasive
turns
known
saccades.5
Saccades
also
be
initiated
spontaneously
change
direction
during
flight.6,7,8,9
Two
types
(DNs),
DNaX
DNb01,
were
previously
shown
exhibit
both
spontaneous
looming-elicited
saccades
Drosophila.10,11
As
they
do
not
receive
direct
system,
it
has
remained
unclear
how
visually
elicited
controlled
by
nervous
system.
receives
looming-sensitive
projection
output
wing
motor
neurons12,13
therefore
promising
candidate
for
saccades.
Using
whole-cell
patch-clamp
recordings
head-fixed
flying
Drosophila,
we
showed
that
ipsilateral
behavioral-state-dependent
manner.
We
further
explored
relates
variable
behavioral
output.
Sustained
activity,
persisting
after
stimulus,
was
strongest
predictor
saccade
execution.
However,
alone
cannot
fully
explain
variability
responses.
Combined
optogenetic
experiments
free
these
results
suggest
important
but
exclusive
role
saccades,
advancing
our
understanding
information
transformed
into
commands
maneuvers
insects.Graphical
abstract
Regenerative Biomaterials,
Journal Year:
2025,
Volume and Issue:
12
Published: Jan. 1, 2025
Abstract
Neurological
injuries
and
diseases
are
a
leading
cause
of
disability
worldwide,
underscoring
the
urgent
need
for
effective
therapies.
Neural
regaining
enhancement
therapies
seen
as
most
promising
strategies
restoring
neural
function,
offering
hope
individuals
affected
by
these
conditions.
Despite
their
promise,
path
from
animal
research
to
clinical
application
is
fraught
with
challenges.
Neuroengineering,
particularly
through
use
biomaterials,
has
emerged
key
field
that
paving
way
innovative
solutions
It
seeks
understand
treat
neurological
disorders,
unravel
nature
consciousness,
explore
mechanisms
memory
brain’s
relationship
behavior,
tissue
engineering,
interfaces
targeted
drug
delivery
systems.
These
including
both
natural
synthetic
types,
designed
replicate
cellular
environment
brain,
thereby
facilitating
repair.
This
review
aims
provide
comprehensive
overview
biomaterials
in
neuroengineering,
highlighting
functional
across
basic
practice.
covers
recent
developments
biomaterial-based
products,
2D
3D
bioprinted
scaffolds
cell
organoid
culture,
brain-on-a-chip
systems,
biomimetic
electrodes
brain–computer
interfaces.
also
explores
artificial
synapses
networks,
discussing
applications
modeling
microenvironments
repair
regeneration,
modulation
manipulation
integration
traditional
Chinese
medicine.
serves
guide
role
advancing
neuroengineering
solutions,
providing
insights
into
ongoing
efforts
bridge
gap
between
innovation
application.
Proceedings of the National Academy of Sciences,
Journal Year:
2025,
Volume and Issue:
122(16)
Published: April 17, 2025
In
order
to
forage
for
food,
many
animals
regulate
not
only
specific
limb
movements
but
the
statistics
of
locomotor
behavior,
switching
between
long-range
dispersal
and
local
search
depending
on
resource
availability.
How
premotor
circuits
is
clear.
Here,
we
analyze
model
their
modulation
by
attractive
food
odor
in
walking
Drosophila
.
Food
evokes
three
motor
regimes
flies:
baseline
walking,
upwind
running
during
odor,
behavior
following
loss.
During
search,
find
that
flies
adopt
higher
angular
velocities
slower
ground
speeds
turn
longer
periods
same
direction.
We
further
different
mean
speed
these
state
changes
influence
length
odor-evoked
runs.
next
developed
a
simple
neural
control
suggests
contralateral
inhibition
plays
key
role
regulating
statistical
features
locomotion.
As
fly
connectome
predicts
decussating
inhibitory
neurons
lateral
accessory
lobe
(LAL),
gained
genetic
access
subset
tested
effects
behavior.
identified
one
population
whose
activation
induces
all
signature
regulates
velocity
at
offset.
second
population,
including
single
LAL
neuron
pair,
bidirectionally
speed.
Together,
our
work
develops
biologically
plausible
computational
architecture
captures
locomotion
across
behavioral
states
identifies
substrates
computations.
PLoS Biology,
Journal Year:
2025,
Volume and Issue:
23(4), P. e3003094 - e3003094
Published: April 21, 2025
How
do
neural
networks
generate
and
regulate
diversity
variability
in
motor
outputs
with
finite
cellular
components?
Here
we
examine
this
problem
by
exploring
the
role
that
inhibitory
neuron
motifs
play
generating
mixtures
of
programs
segmentally
organised
Drosophila
larval
locomotor
system.
We
developed
a
computational
model
is
constrained
experimental
calcium
imaging
data.
The
comprises
single-compartment
cells
single
voltage-gated
current,
which
are
interconnected
graded
excitatory
synapses.
Local
neurons
form
conditional
oscillators
each
hemisegment.
Surrounding
architecture
reflects
key
aspects
inter-
intrasegmental
connectivity
identified
literature.
generates
metachronal
waves
activity
recapitulate
features
fictive
forwards
backwards
locomotion,
as
well
bilaterally
asymmetric
anterior
regions
represents
head
sweeps.
statistics
inputs
to
competing
command-like
motifs,
coupled
detect
across
multiple
segments
network
states
promote
outputs,
while
at
same
time
preventing
maladaptive
overlap
programs.
Overall,
testable
predictions
for
connectomics
physiological
studies
providing
platform
uncovering
how
circuit
underpin
generation
systems.
Nature,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 30, 2025
In
most
complex
nervous
systems
there
is
a
clear
anatomical
separation
between
the
nerve
cord,
which
contains
of
final
motor
outputs
necessary
for
behaviour,
and
brain.
insects,
neck
connective
both
physical
an
information
bottleneck
connecting
brain
ventral
cord
(an
analogue
spinal
cord)
comprises
diverse
populations
descending
neurons
(DNs),
ascending
(ANs)
sensory
neurons,
are
crucial
sensorimotor
signalling
control.
Here,
by
integrating
three
separate
electron
microscopy
(EM)
datasets1-4,
we
provide
complete
connectomic
description
ANs
DNs
Drosophila
female
system
compare
them
with
male
cord.
Proofread
neuronal
reconstructions
matched
across
hemispheres,
datasets
sexes.
Crucially,
also
match
51%
DN
cell
types
to
light-level
data5
defining
specific
driver
lines,
as
well
classifying
all
populations.
We
use
these
results
reveal
circuit
logic
neurons.
observe
connected
chains
spanning
neck,
may
subserve
sequences.
sexually
dimorphic
AN
populations,
detailed
analyses
selected
circuits
reproductive
behaviours,
including
courtship6
(DNa12;
known
aSP22)
song
production7
(AN
from
hemilineage
08B)
ovipositor
extrusion8
(DNp13).
Our
work
provides
EM-level
that
span
entire
central
adult
animal.
Orienting
behaviors
provide
a
continuous
stream
of
information
about
an
organism’s
sensory
experiences
and
plans.
Thus,
to
study
the
links
between
sensation
action,
it
is
useful
identify
neurons
in
brain
that
control
orienting
behaviors.
Here
we
describe
descending
Drosophila
predict
influence
orientation
(heading)
during
walking.
We
show
these
cells
have
specialized
functions:
whereas
one
cell
type
predicts
sustained
low-gain
steering,
other
transient
high-gain
steering.
These
latter
integrate
internally-directed
steering
signals
from
head
direction
system
with
stimulus-directed
multimodal
pathways.
The
inputs
are
organized
produce
“see-saw”
commands,
so
increasing
output
hemisphere
accompanied
by
decreasing
hemisphere.
Together,
our
results
internal
external
drives
integrated
motor
commands
different
timescales,
for
flexible
precise
space.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 12, 2024
Abstract
Animals
construct
diverse
behavioural
repertoires
by
moving
a
limited
number
of
body
parts
with
varied
kinematics
and
patterns
coordination.
There
is
evidence
that
distinct
movements
can
be
generated
changes
in
activity
dynamics
within
common
pool
motoneurons,
or
selectively
engaging
specific
subsets
motoneurons
task-dependent
manner.
However,
most
cases
we
have
an
incomplete
understanding
the
motoneuron
generate
actions
how
upstream
premotor
circuits
select
assemble
such
motor
programmes.
In
this
study,
used
two
closely
related
but
kinematically
types
saccadic
eye
movement
larval
zebrafish
as
model
to
examine
circuit
control
diversity.
contrast
prevailing
view
final
pathway,
found
oculomotor
nucleus,
were
engaged
for
each
saccade
type.
This
type-specific
recruitment
was
topographically
organised
aligned
ultrastructural
differ-ences
morphology
afferent
synaptic
innervation.
Medially
located
motoneu-rons
active
both
tracing
revealed
type-agnostic
pathway
appears
their
recruitment.
By
contrast,
laterally
subset
specifically
hunting-associated
saccades
received
in-put
from
pretectal
hunting
command
neurons.
Our
data
support
which
generalist
action-specific
pathways
engage
elicit
same
part
subserve
functions.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Oct. 12, 2024
Abstract
Animals
rely
on
compensatory
actions
to
maintain
stability
and
navigate
their
environment
efficiently.
These
depend
global
visual
motion
cues
known
as
optic-flow.
While
the
optomotor
response
has
been
traditional
focus
for
studying
optic-flow
compensation
in
insects,
its
simplicity
insufficient
determine
role
of
intricate
processing
network
involved
course
control.
Here,
we
reveal
a
series
control
behaviours
Drosophila
link
them
specific
neural
circuits.
We
show
that
bilateral
electrical
coupling
optic-flow-sensitive
neurons
fly’s
lobula
plate
are
required
proper
This
interaction
works
alongside
chemical
synapses
within
HS-H2
dynamics
direction
turning
behaviours.
Our
findings
how
insects
use
navigation,
assigning
new
functional
significance
suggesting
previously
unknown
gap
junctions
non-linear
operations.
Orienting
behaviors
provide
a
continuous
stream
of
information
about
an
organism’s
sensory
experiences
and
plans.
Thus,
to
study
the
links
between
sensation
action,
it
is
useful
identify
neurons
in
brain
that
control
orienting
behaviors.
Here
we
describe
descending
Drosophila
predict
influence
orientation
(heading)
during
walking.
We
show
these
cells
have
specialized
functions:
whereas
one
cell
type
predicts
sustained
low-gain
steering,
other
transient
high-gain
steering.
These
latter
integrate
internally-directed
steering
signals
from
head
direction
system
with
stimulus-directed
multimodal
pathways.
The
inputs
are
organized
produce
“see-saw”
commands,
so
increasing
output
hemisphere
accompanied
by
decreasing
hemisphere.
Together,
our
results
internal
external
drives
integrated
motor
commands
different
timescales,
for
flexible
precise
space.