bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2022,
Volume and Issue:
unknown
Published: June 3, 2022
Abstract
Respiratory
infection
with
SARS-CoV-2
causes
systemic
vascular
inflammation
and
cognitive
impairment.
We
sought
to
identify
the
underlying
mechanisms
mediating
dysfunction
following
mild
respiratory
infection.
To
this
end,
we
conduced
unbiased
transcriptional
analysis
brain
endothelial
cell
signaling
pathways
dysregulated
by
in
vivo
.
This
revealed
significant
suppression
of
Wnt/β-catenin
signaling,
a
critical
regulator
blood
barrier
integrity.
therefore
hypothesized
that
enhancing
cerebrovascular
activity
would
offer
protection
against
BBB
permeability,
neuroinflammation,
neurological
signs
acute
Indeed,
found
delivery
cerebrovascular-targeted,
engineered
Wnt7a
ligands
protected
integrity,
reduced
T
infiltration
brain,
microglial
activation
Importantly,
therapeutic
strategy
also
mitigated
induced
deficits
novel
object
recognition
assay
for
learning
memory
pole
descent
task
bradykinesia.
These
observations
suggest
enhancement
or
its
downstream
effectors
could
be
potential
interventional
strategies
restoring
health
viral
infections.
Brain,
Journal Year:
2024,
Volume and Issue:
147(5), P. 1636 - 1643
Published: Feb. 2, 2024
Abstract
Respiratory
infection
with
SARS-CoV-2
causes
systemic
vascular
inflammation
and
cognitive
impairment.
We
sought
to
identify
the
underlying
mechanisms
mediating
cerebrovascular
dysfunction
following
mild
respiratory
infection.
To
this
end,
we
performed
unbiased
transcriptional
analysis
brain
endothelial
cell
signalling
pathways
dysregulated
by
mouse
adapted
MA10
in
aged
immunocompetent
C57Bl/6
mice
vivo.
This
revealed
significant
suppression
of
Wnt/β-catenin
signalling,
a
critical
regulator
blood–brain
barrier
(BBB)
integrity.
therefore
hypothesized
that
enhancing
activity
would
offer
protection
against
BBB
permeability,
neuroinflammation,
neurological
signs
acute
Indeed,
found
delivery
cerebrovascular-targeted,
engineered
Wnt7a
ligands
protected
integrity,
reduced
T-cell
infiltration
brain,
microglial
activation
Importantly,
strategy
also
mitigated
induced
deficits
novel
object
recognition
assay
for
learning
memory
pole
descent
task
bradykinesia.
These
observations
suggest
enhancement
or
its
downstream
effectors
could
be
potential
interventional
strategies
restoring
health
viral
infections.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(11), P. 5601 - 5601
Published: May 21, 2024
This
review
addresses
the
role
of
tight
junction
proteins
at
blood-brain
barrier
(BBB).
Their
expression
is
described,
and
their
in
physiological
pathological
processes
BBB
discussed.
Based
on
this,
new
approaches
are
depicted
for
paracellular
drug
delivery
diagnostics
treatment
cerebral
diseases.
Recent
data
provide
convincing
evidence
that,
addition
to
its
impairment
course
diseases,
could
be
involved
aetiology
CNS
disorders.
Further
progress
will
expected
based
insights
protein
structure
involvement
signalling
pathways.
Journal of Neuroimmunology,
Journal Year:
2024,
Volume and Issue:
388, P. 578309 - 578309
Published: Feb. 4, 2024
Blood-brain
barrier
(BBB)
permeability
can
cause
neuroinflammation
and
cognitive
impairment.
Caveolin-1
(Cav-1)
critically
regulates
BBB
permeability,
but
its
influence
on
the
consequent
neurological
outcomes
in
respiratory
viral
infections
is
unknown.
We
used
Cav-1-deficient
mice
with
genetically
encoded
fluorescent
endothelial
tight
junctions
to
determine
how
Cav-1
influences
neuroinflammation,
impairment
following
infection
mouse
adapted
(MA10)
SARS-CoV-2
as
a
model
for
COVID-19.
found
that
increased
brain
transcellular
albumin,
decreased
paracellular
Claudin-5
junctions,
caused
T
lymphocyte
infiltration
hippocampus,
region
important
learning
memory.
Concordantly,
we
observed
memory
deficits
infected
mice.
Importantly,
genetic
deficiency
attenuated
junction
losses,
infiltration,
gliosis
induced
by
infection.
Moreover,
KO
were
protected
from
These
results
establish
contribution
of
behavioral
dysfunction
neuroinflammation.
Science Translational Medicine,
Journal Year:
2024,
Volume and Issue:
16(773)
Published: Nov. 13, 2024
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV
2)
pandemic
has
caused
more
than
7
million
deaths
globally.
Despite
the
presence
of
infection-
and
vaccine-induced
immunity,
SARS-CoV-2
infections
remain
a
major
global
health
concern
because
emergence
variants
that
can
cause
disease
2019
(COVID-19)
or
enhance
Long
Covid
phenotypes.
About
5
to
10%
SARS-CoV-2-infected
individuals
develop
Covid,
which,
similar
COVID
19,
often
affects
lung.
However,
also
affect
other
peripheral
organs,
especially
brain.
causal
relationships
between
phenotypes,
long-term
symptoms,
involvement
multiple
organ
systems
elusive,
animal
model
mimicking
both
post-acute
phases
are
imperative.
Here,
we
review
current
state
models,
including
possible
future
applications.
Lab Animal,
Journal Year:
2023,
Volume and Issue:
52(9), P. 202 - 210
Published: Aug. 24, 2023
Abstract
More
than
40%
of
individuals
infected
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
have
experienced
persistent
or
relapsing
multi-systemic
symptoms
months
after
the
onset
disease
2019
(COVID-19).
This
post-COVID-19
condition
(PCC)
has
debilitating
effects
on
daily
life
patients
and
encompasses
a
broad
spectrum
neurological
neuropsychiatric
including
olfactory
gustative
impairment,
difficulty
with
concentration
short-term
memory,
sleep
disorders
depression.
Animal
models
been
instrumental
to
understand
COVID-19
validate
prophylactic
therapeutic
interventions.
Similarly,
studies
post-viral
clearance
in
hamsters,
mice
nonhuman
primates
inoculated
SARS-CoV-2
useful
unveil
some
aspects
PCC.
Transcriptomic
alterations
central
nervous
system,
activation
immune
cells
impaired
hippocampal
neurogenesis
seem
critical
role
manifestations
observed
animal
SARS-CoV-2.
Interestingly,
proinflammatory
transcriptomic
profile
system
SARS-CoV-2-inoculated
partially
overlaps
pathological
changes
that
affect
microglia
humans
during
Alzheimer’s
aging,
suggesting
shared
mechanisms
between
these
conditions.
None
currently
available
fully
replicates
PCC
humans;
therefore,
multiple
models,
together
fine-tuning
experimental
conditions,
will
probably
be
needed
symptoms.
Moreover,
given
intrinsic
characteristics
new
variants
concern
immunological
status
might
influence
manifestations,
more
are
explore
factors
their
combinations
PCC,
adding
further
complexity
design
models.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(1), P. 98 - 98
Published: Jan. 14, 2025
Post-acute
sequelae
of
COVID-19
(PASC)
are
a
diverse
set
symptoms
and
syndromes
driven
by
dysfunction
multiple
organ
systems
that
can
persist
for
years
negatively
impact
the
quality
life
millions
individuals.
We
currently
lack
specific
therapeutics
patients
with
PASC,
due
in
part
to
an
incomplete
understanding
its
pathogenesis,
especially
non-pulmonary
sequelae.
Here,
we
discuss
three
animal
models
have
been
utilized
investigate
PASC:
non-human
primates
(NHPs),
hamsters,
mice.
focus
on
neurological,
gastrointestinal,
cardiovascular
PASC
highlight
advances
mechanistic
insight
made
using
these
models,
as
well
discussing
warrant
continued
intensive
research.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 26, 2025
Animal
models
are
indispensable
for
unraveling
the
mechanisms
underlying
post-acute
sequelae
of
COVID-19
(PASC).
This
review
evaluates
recent
research
on
PASC-related
perturbations
in
animal
models,
drawing
comparisons
with
clinical
findings.
Despite
limited
number
studies
post-COVID
conditions,
particularly
those
extending
beyond
three
months,
these
provide
valuable
insights.
Three
hallmark
features
PASC-lung
fibrosis,
hyperglycemia,
and
neurological
sequelae-have
been
successfully
replicated
paving
way
mechanistic
discoveries
future
medical
interventions.
Although
most
have
reported
conditions
within
14-60
days
post-infection,
they
still
offer
critical
reference
long-term
research.
also
explores
potential
persisting
immune
misfiring,
a
key
factor
chronicity
PASC
symptoms.
Moreover,
challenges
modeling
discussed,
including
genetic
diversity
inbred
strains
difficulties
accurately
identifying
PASC-affected
individuals.
To
address
issues,
we
propose
methodological
improvements,
such
as
comparing
individual
parameters
control
averages
incorporating
genetically
diverse
populations
like
collaborative
cross
models.
These
strategies
will
enhance
identification
characterization
endotypes
studies.
By
integrating
findings
from
manifestations
PASC,
can
more
insights
into
its
support
development
effective
therapeutic
strategies.
Finally,
emphasize
urgent
need
longitudinal
to
fully
uncover
driving
guide
interventions
mitigate
public
health
impact.
ABSTRACT
Since
the
emergence
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
initiated
a
global
pandemic
resulting
in
an
estimated
775
million
infections
with
over
7
deaths,
it
has
become
evident
that
COVID-19
is
not
solely
pulmonary
disease.
Emerging
evidence
shown
that,
subset
patients,
certain
symptoms
−
including
chest
pain,
stroke,
anosmia,
dysgeusia,
diarrhea
and
abdominal
pain
–
all
indicate
role
vascular,
neurological
gastrointestinal
(GI)
pathology
disease
process.
Many
these
processes
persist
long
after
been
resolved,
‘long
COVID’
or
post-acute
sequelae
(PASC).
The
molecular
mechanisms
underlying
systemic
conditions
associated
remain
incompletely
defined.
Appropriate
animal
models
provide
method
understanding
at
system
level
through
study
progression,
tissue
pathology,
immune
response
to
pathogen
behavioral
responses.
However,
very
few
studies
have
addressed
PASC
whether
existing
hold
promise
for
studying
this
challenging
problem.
Here,
we
review
current
literature
on
cardiovascular,
GI
pathobiology
caused
by
along
established
manifestations
their
prospects
use
studies.
Our
aim
guidance
selection
appropriate
order
recapitulate
aspects
enhance
translatability
mechanistic
Journal of Neurochemistry,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 18, 2023
Abstract
Coronavirus
disease
2019
(COVID‐19)
has
rapidly
escalated
into
a
global
pandemic
that
primarily
affects
older
and
immunocompromised
individuals
due
to
underlying
clinical
conditions
suppressed
immune
responses.
Furthermore,
COVID‐19
patients
exhibit
spectrum
of
neurological
symptoms,
indicating
can
affect
the
brain
in
variety
manners.
Many
studies,
past
recent,
suggest
connection
between
viral
infections
an
increased
risk
neurodegeneration,
raising
concerns
about
effects
possibility
it
may
contribute
Alzheimer's
(AD)
onset
or
worsen
already
existing
AD
pathology
through
inflammatory
processes
given
both
share
pathological
features
factors.
This
leads
us
question
whether
is
factor
for
how
these
two
might
influence
each
other.
Considering
extensive
reach
devastating
impact
ongoing
pandemic,
their
combined
could
have
significant
public
health
consequences
worldwide.
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