Philosophical Transactions of the Royal Society B Biological Sciences,
Journal Year:
2017,
Volume and Issue:
372(1715), P. 20160154 - 20160154
Published: Jan. 17, 2017
Astrocytes
intimately
interact
with
synapses,
both
morphologically
and,
as
evidenced
in
the
past
20
years,
at
functional
level.
Ultrathin
astrocytic
processes
contact
and
sometimes
enwrap
synaptic
elements,
sense
transmission
shape
or
alter
signal
by
releasing
signalling
molecules.
Yet,
consequences
of
such
interactions
terms
information
processing
brain
remain
very
elusive.
This
is
largely
due
to
two
major
constraints:
(i)
exquisitely
complex,
dynamic
ultrathin
nature
distal
that
renders
their
investigation
highly
challenging
(ii)
our
lack
understanding
how
encoded
local
global
fluctuations
intracellular
calcium
concentrations
astrocytes.
Here,
we
will
review
existing
anatomical
evidence
between
astrocytes
it
underlies
a
role
for
computation
information.This
article
part
themed
issue
'Integrating
Hebbian
homeostatic
plasticity'.
Accumulating
evidence
indicates
that
astrocytes
are
actively
involved
in
brain
function
by
regulating
synaptic
activity
and
plasticity.
Different
gliotransmitters,
such
as
glutamate,
ATP,
GABA
or
D-serine,
released
form
have
been
shown
to
induce
different
forms
of
regulation.
However,
whether
a
single
astrocyte
may
release
gliotransmitters
is
unknown.
Here
we
show
mouse
hippocampal
activated
endogenous
(neuron-released
endocannabinoids
GABA)
exogenous
(single
Ca2+
uncaging)
stimuli
modulate
putative
CA3-CA1
synapses.
The
astrocyte-mediated
modulation
was
biphasic
consisted
an
initial
glutamate-mediated
potentiation
followed
purinergic-mediated
depression
neurotransmitter
release.
temporal
dynamic
properties
this
regulation
depended
on
the
firing
frequency
duration
neuronal
stimulated
astrocytes.
Present
results
indicate
can
decode
and,
response,
distinct
differentially
regulate
neurotransmission
at
Neuron,
Journal Year:
2020,
Volume and Issue:
108(5), P. 919 - 936.e11
Published: Sept. 24, 2020
Extrasynaptic
actions
of
glutamate
are
limited
by
high-affinity
transporters
expressed
perisynaptic
astroglial
processes
(PAPs):
this
helps
maintain
point-to-point
transmission
in
excitatory
circuits.
Memory
formation
the
brain
is
associated
with
synaptic
remodeling,
but
how
affects
PAPs
and
therefore
extrasynaptic
poorly
understood.
Here,
we
used
advanced
imaging
methods,
situ
vivo,
to
find
that
a
classical
memory
mechanism,
long-term
potentiation
(LTP),
triggers
withdrawal
from
potentiated
synapses.
Optical
sensors
combined
patch-clamp
3D
molecular
localization
reveal
LTP
induction
thus
prompts
spatial
retreat
transporters,
boosting
spillover
NMDA-receptor-mediated
inter-synaptic
cross-talk.
The
LTP-triggered
PAP
involves
NKCC1
actin-controlling
protein
cofilin
does
not
depend
on
major
Ca
Philosophical Transactions of the Royal Society B Biological Sciences,
Journal Year:
2017,
Volume and Issue:
372(1715), P. 20160154 - 20160154
Published: Jan. 17, 2017
Astrocytes
intimately
interact
with
synapses,
both
morphologically
and,
as
evidenced
in
the
past
20
years,
at
functional
level.
Ultrathin
astrocytic
processes
contact
and
sometimes
enwrap
synaptic
elements,
sense
transmission
shape
or
alter
signal
by
releasing
signalling
molecules.
Yet,
consequences
of
such
interactions
terms
information
processing
brain
remain
very
elusive.
This
is
largely
due
to
two
major
constraints:
(i)
exquisitely
complex,
dynamic
ultrathin
nature
distal
that
renders
their
investigation
highly
challenging
(ii)
our
lack
understanding
how
encoded
local
global
fluctuations
intracellular
calcium
concentrations
astrocytes.
Here,
we
will
review
existing
anatomical
evidence
between
astrocytes
it
underlies
a
role
for
computation
information.This
article
part
themed
issue
'Integrating
Hebbian
homeostatic
plasticity'.