bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 15, 2024
Abstract
Primary
ciliary
dyskinesia
(PCD)
is
a
genetic
disorder
causing
motile
dysfunction
primarily
affecting
the
respiratory
and
reproductive
systems.
However,
impact
of
PCD
on
central
nervous
system,
through
cilia
in
multiciliated
ependymal
cells,
remains
poorly
understood.
We
hypothesized
that
patients
with
exhibit
sub-clinical
ventriculomegaly
due
to
dysfunction,
which
may
influence
neuropsychiatric
diagnoses.
demonstrated
highly
specific
expression
levels
known
PCD-related
genes
human
brain
cells
(
p
<0.0001),
supporting
their
potential
role
regulating
function.
Computed
tomography
sinus
images
from
n
=33)
age/sex-matched
controls
=64)
were
analysed.
Patients
displayed
significantly
larger
ventricular
areas
<0.0001)
Evans
index
<0.01),
indicating
was
consistent
across
all
subgroups.
Ventricular
enlargement
correlated
positively
increasing
age
compared
<0.001).
Chart
review
high
prevalence
(39%)
neuropsychiatric/neurological
disorders
adult
did
not
correlate
degree
ventriculomegaly.
Our
findings
suggest
have
unrecognized,
mild
potentially
correlates
ageing.
Further
study
required
determine
if
contributes
or
other
morbidity
PCD.
Frontiers in Cellular Neuroscience,
Journal Year:
2024,
Volume and Issue:
17
Published: Jan. 8, 2024
The
history
of
research
concerning
ependymal
cells
is
reviewed.
Cilia
were
identified
along
the
surface
cerebral
ventricles
c1835.
Numerous
anatomical
and
histopathological
studies
in
late
1800’s
showed
irregularities
that
thought
to
be
indicative
specific
pathologies
such
as
syphilis;
this
was
subsequently
disproven.
evolution
thoughts
about
functions
cilia,
possible
role
ependyma
brain-cerebrospinal
fluid
barrier,
relationship
subventricular
zone
germinal
discussed.
How
advances
light
electron
microscopy
cell
culture
contributed
our
understanding
described.
Discoveries
supraependymal
serotoninergic
axon
network
macrophages
are
recounted.
Finally,
consequences
loss
from
different
regions
central
nervous
system
considered.
Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(9), P. 2332 - 2332
Published: Aug. 22, 2023
There
is
a
growing
interest
in
glial
cells
the
central
nervous
system
due
to
their
important
role
maintaining
brain
homeostasis
under
physiological
conditions
and
after
injury.
A
significant
amount
of
evidence
has
been
accumulated
regarding
capacity
exert
either
pro-inflammatory
or
anti-inflammatory
effects
different
pathological
conditions.
In
combination
with
proliferative
potential,
they
contribute
not
only
limitation
damage
tissue
remodeling
but
also
neuronal
repair
synaptic
recovery.
Moreover,
reactive
can
modulate
processes
neurogenesis,
differentiation,
migration
neurons
existing
neural
circuits
adult
brain.
By
discovering
precise
signals
within
specific
niches,
regulation
sequential
neurogenesis
holds
potential
unlock
strategies
that
stimulate
generation
functional
neurons,
whether
response
injury
as
means
addressing
degenerative
neurological
Cerebral
ischemic
stroke,
condition
falling
realm
acute
vascular
disorders
affecting
circulation
brain,
stands
prominent
global
cause
disability
mortality.
Extensive
investigations
into
plasticity
intricate
interactions
other
have
predominantly
relied
on
studies
conducted
experimental
animals,
including
rodents
primates.
However,
valuable
insights
gleaned
from
vivo
involving
poststroke
patients,
utilizing
highly
specialized
imaging
techniques.
Following
attempts
map
cells,
various
transcription
factors
modulating
gene
expression
cerebral
ischemia
gaining
increasing
popularity.
Although
results
obtained
thus
far
remain
incomplete
occasionally
ambiguous,
serve
solid
foundation
for
development
aimed
at
influencing
recovery
process
iScience,
Journal Year:
2023,
Volume and Issue:
26(10), P. 107710 - 107710
Published: Aug. 25, 2023
Mice
lacking
caveolin-1
(Cav1),
a
key
protein
of
plasma
membrane,
exhibit
brain
aging
at
an
early
adult
stage.
Here,
integrative
analyses
metabolomics,
transcriptomics,
epigenetics,
and
single-cell
data
were
performed
to
test
the
hypothesis
that
metabolic
deregulation
fetal
due
ablation
Cav1
is
linked
in
these
mice.
The
results
this
study
show
lack
caused
lipid
amino
acid
metabolism
brain,
genes
associated
with
deregulated
metabolites
significantly
altered
upon
aging.
Moreover,
several
specific
cell
types
impacted
DNA
methylation
those
coordination
mouse
epigenetic
clock.
findings
suggest
program
confounded
by
abnormalities
stage
absence
Cav1.
The Journal of Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 6, 2024
Abstract
Background
Nipah
virus
is
an
emerging
zoonotic
that
causes
severe
respiratory
disease
and
meningoencephalitis.
The
pathophysiology
of
meningoencephalitis
poorly
understood.
Methods
We
have
collected
the
brains
African
green
monkeys
during
multiple
virus,
Bangladesh
studies,
resulting
in
14
with
virus-associated
lesions.
Results
lesions
seen
brain
infected
were
very
similar
to
those
observed
humans
Malaysia
infection.
viral
RNA
antigen
within
neurons
endothelial
cells,
encephalitis
foci
uninflamed
portions
central
nervous
system
(CNS).
CD8+
T
cells
had
a
consistently
high
prevalence
CNS
developed
UNet
model
for
quantifying
visualizing
inflammation
high-throughput
unbiased
manner.
While
lesions,
revealed
CD68+
numerically
immune
cell
highest
virus-infected
animals.
Conclusions
Our
study
provides
in-depth
analysis
on
infection
primates,
similarities
between
patients
animals
our
validate
this
model.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 15, 2024
Abstract
Primary
ciliary
dyskinesia
(PCD)
is
a
genetic
disorder
causing
motile
dysfunction
primarily
affecting
the
respiratory
and
reproductive
systems.
However,
impact
of
PCD
on
central
nervous
system,
through
cilia
in
multiciliated
ependymal
cells,
remains
poorly
understood.
We
hypothesized
that
patients
with
exhibit
sub-clinical
ventriculomegaly
due
to
dysfunction,
which
may
influence
neuropsychiatric
diagnoses.
demonstrated
highly
specific
expression
levels
known
PCD-related
genes
human
brain
cells
(
p
<0.0001),
supporting
their
potential
role
regulating
function.
Computed
tomography
sinus
images
from
n
=33)
age/sex-matched
controls
=64)
were
analysed.
Patients
displayed
significantly
larger
ventricular
areas
<0.0001)
Evans
index
<0.01),
indicating
was
consistent
across
all
subgroups.
Ventricular
enlargement
correlated
positively
increasing
age
compared
<0.001).
Chart
review
high
prevalence
(39%)
neuropsychiatric/neurological
disorders
adult
did
not
correlate
degree
ventriculomegaly.
Our
findings
suggest
have
unrecognized,
mild
potentially
correlates
ageing.
Further
study
required
determine
if
contributes
or
other
morbidity
PCD.