Frontiers in Cellular Neuroscience,
Journal Year:
2021,
Volume and Issue:
15
Published: June 7, 2021
The
glial
cells
astrocytes
have
long
been
recognized
as
important
neuron-supporting
elements
in
brain
development,
homeostasis,
and
metabolism.
After
the
discovery
that
reciprocal
communication
between
neurons
is
a
fundamental
mechanism
modulation
of
neuronal
synaptic
communication,
over
last
two
decades
became
hot
topic
neuroscience
research.
Crucial
to
their
functional
interactions
with
are
cytosolic
Ca
2+
elevations
mediate
gliotransmission.
Large
attention
has
posed
so-called
microdomains,
dynamic
changes
spatially
restricted
fine
astrocytic
processes
including
perisynaptic
(PAPs).
With
presynaptic
terminals
postsynaptic
membranes,
PAPs
compose
tripartite
synapse.
distinct
spatial-temporal
features
roles
astrocyte
microdomain
activity
remain
poorly
defined.
However,
thanks
development
genetically
encoded
indicators
(GECIs),
advanced
microscopy
techniques,
innovative
analytical
approaches,
transients
microdomains
were
recently
studied
unprecedented
detail.
These
events
observed
occur
much
more
frequently
(∼50–100-fold)
dynamically
than
somatic
mechanisms
likely
involve
both
IP
3
-dependent
-independent
pathways.
Further
progress
aimed
clarify
complex,
machinery
responsible
for
at
crucial
step
our
understanding
role
function
may
also
reveal
novel
therapeutic
targets
different
diseases.
Here,
we
review
most
recent
studies
improve
mechanistic
essential
microdomains.
Physiological Reviews,
Journal Year:
2017,
Volume and Issue:
98(1), P. 239 - 389
Published: Dec. 24, 2017
Astrocytes
are
neural
cells
of
ectodermal,
neuroepithelial
origin
that
provide
for
homeostasis
and
defense
the
central
nervous
system
(CNS).
highly
heterogeneous
in
morphological
appearance;
they
express
a
multitude
receptors,
channels,
membrane
transporters.
This
complement
underlies
their
remarkable
adaptive
plasticity
defines
functional
maintenance
CNS
development
aging.
tightly
integrated
into
networks
act
within
context
tissue;
astrocytes
control
at
all
levels
organization
from
molecular
to
whole
organ.
Diabetes,
Journal Year:
2014,
Volume and Issue:
63(7), P. 2232 - 2243
Published: June 14, 2014
Insulin
receptors,
as
well
IGF-1
receptors
and
their
postreceptor
signaling
partners,
are
distributed
throughout
the
brain.
acts
on
these
to
modulate
peripheral
metabolism,
including
regulation
of
appetite,
reproductive
function,
body
temperature,
white
fat
mass,
hepatic
glucose
output,
response
hypoglycemia.
also
modulates
neurotransmitter
channel
activity,
brain
cholesterol
synthesis,
mitochondrial
function.
Disruption
insulin
action
in
leads
impairment
neuronal
function
synaptogenesis.
In
addition,
phosphorylation
tau
protein,
an
early
component
development
Alzheimer
disease.
Thus,
alterations
can
contribute
metabolic
syndrome,
mood
disorders
neurodegenerative
diseases.
Frontiers in Human Neuroscience,
Journal Year:
2016,
Volume and Issue:
10
Published: Nov. 8, 2016
Glia
are
essential
for
brain
functioning
during
development
and
in
the
adult
brain.
Here,
we
discuss
various
roles
of
both
microglia
astrocytes,
their
interactions
development.
Although
cells
fundamentally
different
origin
function,
they
often
affect
same
developmental
processes
such
as
neuro-/gliogenesis,
angiogenesis,
axonal
outgrowth,
synaptogenesis
synaptic
pruning.
Due
to
important
instructive
these
processes,
dysfunction
or
astrocytes
could
contribute
neurodevelopmental
disorders
potentially
even
late-onset
neuropathology.
A
better
understanding
origin,
differentiation
process
functions
will
help
fully
appreciate
role
developing
well
brain,
health
disease.
Neural Development,
Journal Year:
2018,
Volume and Issue:
13(1)
Published: April 30, 2018
In
the
mammalian
cerebral
cortex
neurons
are
arranged
in
specific
layers
and
form
connections
both
within
with
other
brain
regions,
thus
forming
a
complex
mesh
of
specialized
synaptic
comprising
distinct
circuits.
The
correct
establishment
these
during
development
is
crucial
for
proper
function
brain.
Astrocytes,
major
type
glial
cell,
important
regulators
synapse
formation
development.
While
neurogenesis
precedes
astrogenesis
cortex,
neuronal
synapses
only
begin
to
after
astrocytes
have
been
generated,
concurrent
branching
process
elaboration.
Here
we
provide
combined
overview
developmental
processes
circuit
rodent
emphasizing
timeline
astrocytic
maturation.
We
further
discuss
role
at
synapse,
focusing
on
astrocyte-synapse
contact
synapse-related
proteins
promoting
cortical
CNS Neuroscience & Therapeutics,
Journal Year:
2019,
Volume and Issue:
25(6), P. 665 - 673
Published: March 30, 2019
Summary
Astrocytes
are
the
most
abundant
glial
cells
in
central
nervous
system
(CNS)
and
participate
synaptic,
circuit,
behavioral
functions.
The
well‐developed
protoplasmic
astrocytes
contain
numerous
processes
forming
well‐delineated
bushy
territories
that
overlap
by
as
little
5%
at
their
boundaries.
This
highly
complex
morphology,
with
up
to
approximately
80%
of
cell's
membrane
constituted
fine
dimensions
on
tens
nanometer
scale
high
surface
area
volume
ratios,
comes
contact
synapses,
blood
vessels,
other
cells.
Recent
progress
is
challenging
conventional
view
morphologically
homogeneous
throughout
brain;
instead,
they
display
circuit‐
region‐specific
morphological
diversity
may
contribute
heterogeneous
astrocyte‐neuron
spatiotemporal
interplay
different
brain
areas.
Further,
structure
found
be
plastic
activity‐dependent.
We
beginning
understand
how
astrocyte
structural
plasticity
contributes
change/loss
traditionally
known
a
hallmark
for
reactive
astrogliosis,
common
pathological
feature
many
neurological
disorders.
However,
recent
data
suggest
deficits
preceding
astrogliosis
drive
disease
progression.
review
summarizes
advances
diversity,
plasticity,
disease‐related
deficits.
Glia,
Journal Year:
2022,
Volume and Issue:
70(8), P. 1467 - 1483
Published: May 10, 2022
Abstract
Brain
circuits
undergo
substantial
structural
changes
during
development,
driven
by
the
formation,
stabilization,
and
elimination
of
synapses.
Synaptic
connections
continue
to
experience‐dependent
rearrangements
throughout
life,
which
are
postulated
underlie
learning
memory.
Astrocytes,
a
major
glial
cell
type
in
brain,
physically
contact
with
synaptic
through
their
ensheathment
Astrocytes
strongly
contribute
remodeling
structures
healthy
diseased
central
nervous
systems
regulating
connectivity
behaviors.
However,
whether
plasticity
astrocytes
is
involved
critical
functions
at
synapse
unknown.
This
review
will
discuss
emerging
evidence
linking
astrocytic
circuit
regulation
Moreover,
we
survey
possible
molecular
cellular
mechanisms
non‐cell‐autonomous
effects
on
neuronal
plasticity.
Finally,
how
astrocyte
morphological
different
physiological
states
disease
conditions
function
dysfunction.
BMC Biology,
Journal Year:
2015,
Volume and Issue:
13(1)
Published: Aug. 24, 2015
Astrocytes
can
mediate
neurovascular
coupling,
modulate
neuronal
excitability,
and
promote
synaptic
maturation
remodeling.
All
these
functions
are
likely
to
be
modulated
by
the
sleep/wake
cycle,
because
brain
metabolism,
activity
turnover
change
as
a
function
of
behavioral
state.
Yet,
little
is
known
about
effects
sleep
wake
on
astrocytes.
Here
we
show
that
strongly
affect
both
astrocytic
gene
expression
ultrastructure
in
mouse
brain.
Using
translating
ribosome
affinity
purification
technology
microarrays,
find
1.4
%
all
transcripts
forebrain
dependent
state
(three
groups,
sleep,
wake,
short
deprivation;
six
mice
per
group).
Sleep
upregulates
few
select
genes,
like
Cirp
Uba1,
whereas
many
genes
related
extracellular
matrix
cytoskeleton,
including
Trio,
Synj2
Gem,
which
involved
elongation
peripheral
processes.
serial
block
face
scanning
electron
microscopy
deprivation,
chronic
restriction;
three
group,
>100
spines
mouse,
3D),
hours
sufficient
bring
processes
closer
cleft,
while
restriction
also
extends
overall
coverage
synapse,
at
axon–spine
interface,
increases
available
surface
neuropil.
Wake-related
changes
reflect
an
increased
need
for
glutamate
clearance,
consistent
with
increase
strength
when
prevented.
The
reduced
during
instead,
may
favor
spillover,
thus
promoting
synchronization
non-rapid
eye
movement
sleep.
Cold Spring Harbor Perspectives in Biology,
Journal Year:
2015,
Volume and Issue:
unknown, P. a020396 - a020396
Published: Feb. 13, 2015
Bruno
Weber1
and
L.
Felipe
Barros2
1University
of
Zürich,
Institute
Pharmacology
Toxicology,
8057
Switzerland
2Centro
de
Estudios
Científicos,
Casilla
1469,
Valdivia,
Chile
Correspondence:
bweber{at}pharma.uzh.ch;
fbarros{at}cecs.cl