This
doctoral
thesis
identifies
sex
differences
in
neocortical
astroglial
cells
over
development
and
delineates
the
role
of
masculinizing
hormones
inducing
these
differences.
Furthermore,
we
identify
astroglia
gene
protein
expression
patterns
across
estrous
cycle
adulthood.
Astroglial
have
emerged
as
key
regulators
brain
health
disease,
they
are
involved
various
aspects
neurodevelopment,
including
organization,
synapse
maturation,
blood-brain
barrier
development.
Additionally,
build,
maintain,
regulate
neuronal
networks
through
close
modulation
neurotransmission
synaptic
plasticity
These
studies
utilized
an
Aldh1l1-L10a-eGFP
mouse
line
translating
ribosome
affinity
purification
with
RNA
sequencing
(TRAPseq)
to
investigate
at
six
developmental
time
points
during
four
different
phases
cycle.
We
found
two
distinct
phenotypes:
"early"/developmental
phenotype
a
"late"/mature
phenotype.
Male
mature
more
rapidly,
reaching
by
postnatal
day
7
(P7),
than
female
astroglia,
which
reach
between
P7-P14.
then
investigated
effects
neonatal
administration
estradiol
females,
resulted
changes
rates
maturation.
During
adulthood,
there
were
no
significant
cell
when
females
observed
on
metestrus,
circulating
levels
ovarian
lowest,
however,
cycle,
proestrus
phase
being
most
from
males.
findings
provide
insight
into
suggest
potential
functional
implications
that
may
lead
disparities
neurodevelopmental
psychiatric
disorders.
As
play
crucial
maintaining
structural
integrity
brain,
it
is
understand
how
gonadal
influence
their
differentiation
function.
Further
research
needed
fully
specific
50
mechanisms
underlie
51
contribute
Nature,
Journal Year:
2024,
Volume and Issue:
627(8004), P. 604 - 611
Published: March 6, 2024
Abstract
Human
brains
vary
across
people
and
over
time;
such
variation
is
not
yet
understood
in
cellular
terms.
Here
we
describe
a
relationship
between
people’s
cortical
neurons
astrocytes.
We
used
single-nucleus
RNA
sequencing
to
analyse
the
prefrontal
cortex
of
191
human
donors
aged
22–97
years,
including
healthy
individuals
with
schizophrenia.
Latent-factor
analysis
these
data
revealed
that,
whose
more
strongly
expressed
genes
encoding
synaptic
components,
astrocytes
distinct
functions
for
synthesizing
cholesterol,
an
astrocyte-supplied
component
membranes.
call
this
neuron
astrocyte
program
(SNAP).
In
schizophrenia
ageing—two
conditions
that
involve
declines
cognitive
flexibility
plasticity
1,2
—cells
divested
from
SNAP:
astrocytes,
glutamatergic
(excitatory)
GABAergic
(inhibitory)
all
showed
reduced
SNAP
expression
corresponding
degrees.
The
astrocytic
neuronal
components
both
involved
which
genetic
risk
factors
were
concentrated.
SNAP,
varies
quantitatively
even
among
similar
age,
may
underlie
many
aspects
normal
interindividual
differences
be
important
point
convergence
multiple
kinds
pathophysiology.
Dental and Medical Problems,
Journal Year:
2023,
Volume and Issue:
61(1), P. 43 - 52
Published: Oct. 20, 2023
Background.Obstructive
sleep
apnea
(OSA)
and
arterial
hypertension
(AH)
are
closely
linked
disorders
with
common
pathophysiological
features.Objectives.The
present
study
aimed
to
investigate
the
relationship
between
AH
OSA
by
examining
architecture,
vitamin
D
concentration
electrolyte
levels
in
patients
these
coexisting
conditions.
Material
methods.A
total
of
133
suspected
having
were
recruited
for
examination.The
participants
divided
into
2
groups:
hypertensives
(n
=
52);
normotensives
81).One
full-night
polysomnographic
examinations
conducted,
followed
statistical
analysis
collected
data.
Results.Hypertensive
individuals
displayed
increased
apnea-hypopnea
index
(AHI),
oxygen
desaturation
(ODI),
respiratory
arousal
(RAI),
periodic
limb
movement
(PLMI)
as
compared
non-hypertensive
individuals.Moreover,
efficiency
(SE),
bruxism
(BAI)
saturation
(SpO
)
level
decreased
hypertensive
group.In
terms
biochemical
parameters,
exhibited
a
lower
magnesium
(Mg)
level,
higher
C-reactive
protein
(CRP),
uric
acid
(UA)
glucose.Notably,
there
no
differences
normotensive
individuals.
Conclusions.The
explored
potential
influence
calcium
(Ca),
Mg,
D,
UA
concentrations
on
architecture
comorbid
OSA.The
findings
revealed
several
notable
associations.Firstly,
fragmentation
correlated
Ca
suggesting
role
both
arousals.Secondly,
was
AHI
fragmentation.Additionally,
alterations
Mg
observed
among
OSA.However,
further
research
is
needed
fully
comprehend
impact
factors
apnea.
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
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 22, 2024
Abstract
Locus
coeruleus
(LC)-derived
norepinephrine
(NE)
drives
network
and
behavioral
adaptations
to
environmental
saliencies
by
reconfiguring
circuit
connectivity,
but
the
underlying
synapse-level
mechanisms
are
elusive.
Here,
we
show
that
NE
remodeling
of
synaptic
function
is
independent
from
its
binding
on
neuronal
receptors.
Instead,
astrocytic
adrenergic
receptors
Ca
2+
dynamics
fully
gate
effect
synapses
as
astrocyte-specific
deletion
three
astrocyte-silencing
approaches
all
render
insensitive
NE.
Additionally,
find
suppression
strength
results
an
ATP-derived
adenosine
A1
receptor-mediated
control
presynaptic
efficacy.
An
accompanying
study
Chen
et
al.
reveals
existence
analogous
pathway
in
larval
zebrafish
highlights
importance
state
transitions.
Together,
these
findings
fuel
a
new
model
wherein
astrocytes
core
component
neuromodulatory
systems
effector
through
which
produces
adaptations,
challenging
80-year-old
status
quo.
Cell Calcium,
Journal Year:
2024,
Volume and Issue:
118, P. 102855 - 102855
Published: Feb. 7, 2024
Chloride
ions
(Cl−)
play
a
pivotal
role
in
synaptic
inhibition
the
central
nervous
system,
primarily
mediated
through
ionotropic
mechanisms.
A
recent
breakthrough
emphathizes
significant
influence
of
astrocytic
intracellular
chloride
concentration
([Cl−]i)
regulation,
field
still
its
early
stages
exploration.
Typically,
[Cl−]i
most
animal
cells
is
maintained
at
lower
levels
than
extracellular
[Cl−]o,
critical
balance
to
prevent
cell
swelling
due
osmotic
pressure.
Various
Cl−
transporters
are
expressed
differently
across
types,
fine-tuning
[Cl−]i,
while
gradients
utilised
by
several
families
channels.
Although
passive
distribution
within
governed
basic
biophysical
principles,
astrocytes
actively
expend
energy
sustain
much
higher
those
achieved
passively,
and
neuronal
[Cl−]i.
Beyond
volume
dynamically
linked
brain
states
influences
signalling
behaving
animals.
As
vital
component
function,
also
plays
development
disorders
where
inhibitory
transmission
disrupted.
This
review
synthesises
latest
insights
into
elucidating
modulating
function
implications
various
pathophysiological
conditions.
The
posterior
parietal
cortex
(
PPC
)
in
mice
has
various
functions
including
multisensory
integration
1–3
,
vision-guided
behaviors
4–6
working
memory
7–13
and
posture
control
14,15
.
However,
an
integrated
understanding
of
these
their
cortical
localizations
around
the
higher
visual
areas
HVAs
),
not
been
completely
elucidated.
Here
we
simultaneously
imaged
activity
thousands
neurons
within
a
3
x
mm
2
field-of-view,
eight
PPC,
during
behavior
with
two-photon
mesoscope
16
Mice
performed
both
task
choice
history-dependent
task,
imaging
results
revealed
distinct,
localized,
behavior-related
two
medial
areas.
Neurons
anteromedial
AM
HVA
responded
to
vision
information,
thus
is
locus
association
between
channels.
By
contrast,
anterior
A
stores
history
sequential
dynamics
represents
posture.
Mesoscale
correlation
analysis
on
intertrial
variability
neuronal
demonstrated
that
area
shared
fluctuations
primary
somatosensory
area,
while
exhibited
diverse,
area-dependent
interactions.
Pairwise
interarea
interactions
among
were
precisely
predicted
by
anatomical
input
correlations,
exception
some
global
Thus,
distinct
modules,
AM,
which
each
have
distinctive
modes
communication.
These
modules
can
serve
separate
higher-order
functions:
for
transmission
information
posture,
movement,
memory;
cognitive
locally
processed
signals.
The
posterior
parietal
cortex
(
PPC
)
in
mice
has
various
functions
including
multisensory
integration
1–3
,
vision-guided
behaviors
4–6
working
memory
7–13
and
posture
control
14,15
.
However,
an
integrated
understanding
of
these
their
cortical
localizations
around
the
higher
visual
areas
HVAs
),
not
been
completely
elucidated.
Here
we
simultaneously
imaged
activity
thousands
neurons
within
a
3
x
mm
2
field-of-view,
eight
PPC,
during
behavior
with
two-photon
mesoscope
16
Mice
performed
both
task
choice
history-dependent
task,
imaging
results
revealed
distinct,
localized,
behavior-related
two
medial
areas.
Neurons
anteromedial
AM
HVA
responded
to
vision
information,
thus
is
locus
association
between
channels.
By
contrast,
anterior
A
stores
history
sequential
dynamics
represents
posture.
Mesoscale
correlation
analysis
on
intertrial
variability
neuronal
demonstrated
that
area
shared
fluctuations
primary
somatosensory
area,
while
exhibited
diverse,
area-dependent
interactions.
Pairwise
interarea
interactions
among
were
precisely
predicted
by
anatomical
input
correlations,
exception
some
global
Thus,
distinct
modules,
AM,
which
each
have
distinctive
modes
communication.
These
modules
can
serve
separate
higher-order
functions:
for
transmission
information
posture,
movement,
memory;
cognitive
locally
processed
signals.
Journal of Neurochemistry,
Journal Year:
2025,
Volume and Issue:
169(2)
Published: Feb. 1, 2025
ABSTRACT
Cortical
damage
and
dysfunction
is
a
pathological
hallmark
of
multiple
sclerosis
(MS)
that
correlates
with
the
severity
physical
cognitive
disability.
Astrocytes
participate
in
MS
pathobiology
through
variety
mechanisms,
abnormal
astrocytic
calcium
signaling
has
been
pointed
as
pathogenic
mechanism
cortical
MS.
However,
vivo
evidence
supporting
deregulation
astrocyte
calcium‐dependent
mechanisms
still
limited.
Here,
we
applied
fiber
photometry
to
longitudinal
analysis
spontaneous
sensory‐evoked
network
activity
somatosensory
cortex
mice
an
experimental
autoimmune
encephalomyelitis
(EAE).
We
found
freely
moving
EAE
exhibit
spontaneously
occurring
signals
increased
duration
reduced
amplitude.
Concomitantly,
astrocytes
responded
sensory
stimulation
events
decreased
The
emergence
aberrant
paralleled
onset
neurological
symptomatology,
changes
amplitude
both
evoked
responses
were
selectively
correlated
deficits.
These
results
highlight
imbalance
brain
during
inflammation
further
support
relevance
astrocyte‐based
underlying
image