The Journal of Cell Biology,
Journal Year:
2023,
Volume and Issue:
222(11)
Published: Oct. 19, 2023
An
astrocyte's
intricate
morphology
is
essential
for
proper
brain
function,
but
the
intrinsic
and
extrinsic
cues
that
set
astrocyte
are
largely
unknown.
In
this
issue,
Tan
et
al.
(https://doi.org/10.1083/jcb.202303138)
show
layer-specific
expression
of
neuronal
cadherins
locally
regulates
morphogenesis
heterogeneity.
Trends in Cell Biology,
Journal Year:
2023,
Volume and Issue:
34(7), P. 547 - 565
Published: Oct. 26, 2023
Astrocytes
are
predominant
glial
cells
that
tile
the
central
nervous
system
(CNS).
A
cardinal
feature
of
astrocytes
is
their
complex
and
visually
enchanting
morphology,
referred
to
as
bushy,
spongy,
star-like.
precept
this
review
such
morphological
shapes
evolved
allow
contact
signal
with
diverse
at
a
range
distances
in
order
sample,
regulate,
contribute
extracellular
milieu,
thus
participate
widely
cell–cell
signaling
during
physiology
disease.
The
recent
use
improved
imaging
methods
cell-specific
molecular
evaluations
has
revealed
new
information
on
structural
organization
underpinnings
astrocyte
mechanisms
morphogenesis,
contributions
disease
states
reduced
morphology.
These
insights
have
reignited
interest
complexity
cornerstone
fundamental
biology
critical
substrate
for
multicellular
spatial
physiological
interactions
CNS.
Trends in Neurosciences,
Journal Year:
2024,
Volume and Issue:
47(4), P. 289 - 302
Published: March 22, 2024
Selective
vulnerability
of
specific
brain
regions
and
cell
populations
is
a
hallmark
neurodegenerative
disorders.
Mechanisms
selective
involve
neuronal
heterogeneity,
functional
specializations,
differential
sensitivities
to
stressors
pathogenic
factors.
In
this
review
we
discuss
the
growing
body
literature
suggesting
that,
like
neurons,
astrocytes
are
heterogeneous
specialized,
respond
integrate
diverse
inputs,
induce
effects
on
function.
disease,
undergo
specific,
context-dependent
changes
that
promote
different
trajectories
outcomes.
We
propose
contribute
through
maladaptive
transitions
context-divergent
phenotypes
impair
functions.
Further
studies
multifaceted
roles
in
disease
may
provide
new
therapeutic
approaches
enhance
resilience
against
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 18, 2025
Abstract
The
Cri
du
Chat
Syndrome
(CdCS),
a
devastating
genetic
disorder
caused
by
deletion
on
chromosome
5p,
faces
challenges
in
finding
effective
treatments
and
accurate
animal
models.
Using
CRISPR‐Cas9,
novel
CdCS
rat
model
with
2q22
is
developed,
mirroring
common
alteration
patients.
This
exhibits
pronounced
deficits
social
behavior,
cognition,
anxiety,
accompanied
neuronal
abnormalities
immune
dysregulation
key
brain
regions
such
as
the
hippocampus
medial
prefrontal
cortex
(mPFC).
immunostaining
RNA‐seq
analyses
provide
new
insights
into
pathogenesis,
revealing
inflammatory
processes.
Importantly,
it
demonstrated
that
early
gene
replacement
therapy
AAV‐
Ctnnd2
alleviates
cognitive
impairments
rats,
highlighting
potential
for
intervention.
However,
effectiveness
of
this
confined
to
developmental
stages
does
not
fully
restore
all
symptoms.
findings
deepen
understanding
pathogenesis
suggest
promising
therapeutic
directions.
The Journal of Physiology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 27, 2025
Abstract
Astrocytes,
the
most
abundant
glial
cells
in
brain,
are
wired
into
neural
circuits
through
close
contact
with
neuronal
pre‐
and
post‐synapses,
called
tripartite
synapses.
The
mutual
communication
between
neurons
astrocytes
is
crucial
for
circuit
dynamics
animal
behaviour.
Recent
advancements
imaging,
manipulation
transcriptomics
have
revealed
that
exhibit
spatiotemporally
complex
computations
represent
circuit‐specialised
functions
molecular
makeups.
However,
understanding
neuron–astrocyte
circuitry
by
means
of
conventional
anatomical
methods
hindered
due
to
technical
limitations.
In
this
review,
we
highlight
recently
developed
optical,
genetic
viral
techniques
enable
high‐throughput
identification
connected
pairs
specificity.
These
approaches
will
accelerate
functional
dissections
health
disease
future
studies.
image
Cells,
Journal Year:
2024,
Volume and Issue:
13(10), P. 837 - 837
Published: May 14, 2024
In
recent
decades,
there
has
been
a
dramatic
rise
in
the
rates
of
children
being
born
after
utero
exposure
to
drugs
abuse,
particularly
opioids.
Opioids
have
shown
detrimental
effects
on
neurons
and
glia
central
nervous
system
(CNS),
but
impact
prenatal
opioid
(POE)
still-developing
synaptic
circuitry
is
largely
unknown.
Astrocytes
exert
powerful
influence
development,
secreting
factors
either
promote
or
inhibit
synapse
formation
neuronal
maturation
developing
CNS.
Here,
we
investigated
partial
µ-opioid
receptor
agonist
buprenorphine
astrocyte
synaptogenic
signaling
morphological
development
cortical
cell
culture.
Acute
treatment
had
no
effect
excitatory
number
astrocyte-free
neuron
cultures.
conditions
where
shared
culture
media
with
astrocytes,
attenuated
capabilities
astrocyte-secreted
factors.
Neurons
cultured
from
drug-naïve
mice
showed
change
synapses
when
treated
secreted
by
astrocytes
POE
mice.
However,
this
same
was
applied
mice,
indicating
complex
neuroadaptive
response
event
impaired
signaling.
addition
promoting
connectivity
changes
neurons,
exerted
strong
disrupting
their
structural
accumulation
lipid
droplets
(LDs),
suggestive
maladaptive
stress
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 11, 2024
Adherens
junctions
(AJs)
are
a
fundamental
organizing
structure
for
multicellular
life.
Although
AJs
studied
mainly
in
epithelia,
their
core
function
-
stabilizing
cell
contacts
by
coupling
adhesion
molecules
to
the
cytoskeleton
is
important
diverse
tissues.
We
find
that
two
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 23, 2024
ABSTRACT
Dysfunctional
mitochondrial
dynamics
are
a
hallmark
of
devastating
neurodevelopmental
disorders
such
as
childhood
refractory
epilepsy.
However,
the
role
glial
mitochondria
in
proper
brain
development
is
not
well
understood.
We
show
that
astrocyte
undergo
extensive
fission
while
populating
distal
branches
during
postnatal
cortical
development.
Loss
regulator,
Dynamin-related
protein
1
(Drp1),
decreases
localization
to
processes,
and
this
mislocalization
reduces
morphological
complexity.
Functionally,
astrocyte-specific
conditional
deletion
Drp1
induces
reactivity
disrupts
organization
cortex.
These
organizational
deficits
accompanied
by
loss
astrocytic
gap
junction
Connexin
43.
findings
uncover
crucial
for
coordinating
morphogenesis
organization,
revealing
regulation
critical
step
neurodevelopment.
Summary
During
morphogenesis,
decrease
size
populate
processes.
Drp1-mediated
necessary
peripheral
process
formation.
Astrocyte-specific
reactivity,
dysregulates
gap-junction
43
abundance.