bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2020,
Volume and Issue:
unknown
Published: April 5, 2020
Abstract
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.
Dopaminergic
neurons
with
distinct
projection
patterns
and
physiological
properties
compose
memory
subsystems
in
a
brain.
However,
it
is
poorly
understood
whether
or
how
they
interact
during
complex
learning.
Here,
we
identify
feedforward
circuit
formed
between
dopamine
show
that
essential
for
second-order
conditioning,
an
ethologically
important
form
of
higher-order
associative
The
Drosophila
mushroom
body
comprises
series
dopaminergic
compartments,
each
which
exhibits
dynamics.
We
find
slow
stable
compartment
can
serve
as
effective
‘teacher’
by
instructing
other
faster
transient
compartments
via
single
key
interneuron,
connectome
analysis
neurotransmitter
prediction.
This
excitatory
interneuron
acquires
enhanced
response
to
reward-predicting
odor
after
first-order
conditioning
and,
upon
activation,
evokes
release
the
‘student’
compartments.
These
hierarchical
connections
explain
first-
long
known
behavioral
psychologists.
Proceedings of the National Academy of Sciences,
Journal Year:
2017,
Volume and Issue:
114(26), P. 6666 - 6674
Published: June 13, 2017
Nervous
systems
use
excitatory
cell
assemblies
to
encode
and
represent
sensory
percepts.
Similarly,
synaptically
connected
or
"engrams"
are
thought
memories
of
past
experience.
Multiple
lines
recent
evidence
indicate
that
brain
create
inhibitory
replicas
representations
for
important
cognitive
functions.
Such
matched
"inhibitory
engrams"
can
form
through
homeostatic
potentiation
inhibition
onto
postsynaptic
cells
show
increased
levels
excitation.
Inhibitory
engrams
reduce
behavioral
responses
familiar
stimuli,
thereby
resulting
in
habituation.
In
addition,
by
preventing
inappropriate
activation
memory
engrams,
make
quiescent,
stored
a
latent
is
available
context-relevant
activation.
neural
networks
with
balanced
the
release
innate
recall
associative
occur
focused
disinhibition.
Understanding
mechanisms
regulate
formation
expression
vivo
may
help
not
only
explain
key
features
cognition
but
also
provide
insight
into
transdiagnostic
traits
associated
psychiatric
conditions
such
as
autism,
schizophrenia,
posttraumatic
stress
disorder.
Cell Reports,
Journal Year:
2018,
Volume and Issue:
25(3), P. 651 - 662.e5
Published: Oct. 1, 2018
It
remains
unclear
how
memory
engrams
are
altered
by
experience,
such
as
new
learning,
to
cause
forgetting.
Here,
we
report
that
short-term
aversive
in
Drosophila
is
encoded
and
retrieved
from
the
mushroom
body
output
neuron
MBOn-γ2α′1.
Pairing
an
odor
with
electric
shock
creates
a
robust
depression
calcium
response
of
MBOn-γ2α′1
increases
avoidance
paired
odor.
Electric
after
which
activates
cognate
dopamine
DAn-γ2α′1,
restores
properties
causes
behavioral
Conditioning
second
responses
previously
learned
while
depressing
newly
odor,
showing
learning
forgetting
can
occur
simultaneously.
Moreover,
optogenetic
activation
DAn-γ2α′1
sufficient
for
bidirectional
modulation
properties.
Thus,
single
DAn
drive
both
bidirectionally
modulating
cellular
trace.
Neuron,
Journal Year:
2019,
Volume and Issue:
104(3), P. 544 - 558.e6
Published: Aug. 27, 2019
In
pursuit
of
food,
hungry
animals
mobilize
significant
energy
resources
and
overcome
exhaustion
fear.
How
need
motivation
control
the
decision
to
continue
or
change
behavior
is
not
understood.
Using
a
single
fly
treadmill,
we
show
that
flies
persistently
track
food
odor
increase
their
effort
over
repeated
trials
in
absence
reward
suggesting
dominates
negative
experience.
We
further
tracking
regulated
by
two
mushroom
body
output
neurons
(MBONs)
connecting
MB
lateral
horn.
These
MBONs,
together
with
dopaminergic
Dop1R2
signaling,
behavioral
persistence.
Conversely,
an
octopaminergic
neuron,
VPM4,
which
directly
innervates
one
acts
as
brake
on
feeding
olfaction.
Together,
our
data
suggest
function
for
internal
state-dependent
expression
can
be
suppressed
external
inputs
conveying
competing
drive.
Open Biology,
Journal Year:
2019,
Volume and Issue:
9(3)
Published: March 1, 2019
Hunger
is
a
motivational
state
that
drives
eating
and
food-seeking
behaviour.
In
psychological
sense,
hunger
sets
the
goal
guides
an
animal
in
pursuit
of
food.
The
biological
basis
underlying
this
purposive,
goal-directed
nature
has
been
under
intense
investigation.
With
its
rich
behavioural
repertoire
genetically
tractable
nervous
system,
fruit
fly
Drosophila
melanogaster
emerged
as
excellent
model
system
for
studying
neural
hunger-driven
Here,
we
review
our
current
understanding
how
sensed,
encoded
translated
into
foraging
feeding
behaviours
fly.
Neuron,
Journal Year:
2020,
Volume and Issue:
106(6), P. 977 - 991.e4
Published: April 13, 2020
Forming
long-term
memory
(LTM)
often
requires
repetitive
experience
spread
over
time.
Studies
in
Drosophila
suggest
aversive
olfactory
LTM
is
optimal
after
spaced
training,
multiple
trials
of
differential
odor
conditioning
with
rest
intervals.
Memory
training
frequently
compared
to
that
the
same
number
without
Here
we
show
that,
flies
acquire
additional
information
and
form
an
for
shock-paired
a
slowly
emerging
more
persistent
"safety-memory"
explicitly
unpaired
odor.
Safety-memory
acquisition
repetition,
order,
spacing
relies
on
triggering
specific
rewarding
dopaminergic
neurons.
Co-existence
safety
memories
evident
as
depression
odor-specific
responses
at
different
combinations
junctions
mushroom
body
output
network;
combining
two
outputs
appears
signal
relative
safety.
Having
complementary
augments
performance
by
making
preference
certain.
Current
thought
envisions
dopamine
neurons
conveying
the
reinforcing
effect
of
unconditioned
stimulus
during
associative
learning
to
axons
Drosophila
mushroom
body
Kenyon
cells
for
normal
olfactory
learning.
Here,
we
show
using
functional
GFP
reconstitution
experiments
that
and
from
axoaxonic
reciprocal
synapses.
The
receive
cholinergic
input
via
nicotinic
acetylcholine
receptors
cells;
knocking
down
these
impairs
revealing
importance
at
synapse.
Blocking
synaptic
output
conditioning
reduces
presynaptic
calcium
transients
in
neurons,
a
finding
consistent
with
communication.
Moreover,
silencing
decreases
chronic
activity
neurons.
Our
results
reveal
new
critical
role
positive
feedback
onto
through
connections