Clinical Cardiology,
Год журнала:
2024,
Номер
48(1)
Опубликована: Дек. 20, 2024
The
association
between
the
expression
of
type
I
interferon
related
genes
(TIIRGs)
and
EFrHF
is
not
well
understood.
This
study
aimed
to
investigate
correlation
patterns
TIIRGs
using
bioinformatics
analysis.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(2), С. 705 - 705
Опубликована: Янв. 15, 2025
Peripheral
blood
mononuclear
cells'
(PBMCs)
mitochondrial
respiration
is
impaired
and
likely
involved
in
myocardial
injury
heart
failure
pathophysiology,
but
its
response
to
acute
severe
hypoxia,
often
associated
with
such
diseases,
largely
unknown
humans.
We
therefore
determined
the
effects
of
hypoxia
on
PBMC
ROS
production
healthy
volunteers
exposed
controlled
oxygen
reduction,
achieving
an
inspired
fraction
10.5%.
also
investigated
potential
relationships
gene
expression
key
biomarkers
succinate
inflammation,
as
inflammation
share
common
mechanisms
cardiovascular
disease.
Unlike
global
respiration,
hypoxemia
a
spO2
≤
80%
significantly
reduced
complex
II
(from
6.5
±
1.2
3.1
0.5
pmol/s/106
cell,
p
=
0.04).
Complex
activity
correlated
positively
(r
0.63,
0.02)
inversely
receptor
SUCNR1
-0.68),
alpha-subunit
hypoxia-inducible
factor
(HIF-1α,
r
-0.61),
chemokine
ligand-9
-0.68)
interferon-stimulated
15
-0.75).
In
conclusion,
specifically
impairs
association
succinate,
HIF-1α
pathway
interactions
human
PBMCs.
These
results
support
further
studies
investigating
whether
modulation
might
modify
inflammatory
metabolic
alterations
observed
failure.
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 4, 2025
Abstract
Restrictive
cardiomyopathy
(RCM)
is
a
rare,
fatal
disorder
that
rapidly
progresses
in
children.
TNNI3
mutations
represent
the
most
common
genetic
cause.
Although
cTnI
are
known
to
increase
myofilament
calcium
sensitivity
and
impair
diastolic
function,
this
mechanism
alone
does
not
fully
account
for
disease
pathogenesis.
Recent
studies
have
revealed
immune
system
plays
an
important
role
cardiovascular
diseases,
however,
its
involvement
RCM
remains
unclear.
Here,
we
generated
classic
cTnIR193H
mouse
model
using
CRISPR/Cas9.
Cardiac
RNA-seq
analysis
indicated
marked
activation
of
innate
pathways.
moreover,
biotin-mediated
proximity
labeling
combined
with
quantitative
mass
spectrometry
identified
differential
interactors
mutant,
Irgm1
emerging
as
significantly
altered
immune-related
protein.
Notably,
mutation
enhances
binding
without
affecting
expression,
thereby
indirectly
inhibiting
normal
function.
This
aberrant
interaction
activates
cGAS-STING
pathway
elicits
type
I
interferon
response
hearts
mice.
Furthermore,
treatment
STING
inhibitor
C176
partially
restored
function
alleviated
cardiac
fibrosis.
Taken
together,
study
reveals
first
time
mechanisms
play
crucial
pathogenesis
provides
potential
therapeutic
target
from
immunological
perspective.
Seminars in Cell and Developmental Biology,
Год журнала:
2025,
Номер
171, С. 103612 - 103612
Опубликована: Апрель 29, 2025
Cardiovascular
diseases
remain
the
leading
cause
of
death
worldwide-claiming
one-third
all
deaths
every
year.
Current
two-dimensional
in
vitro
cell
culture
systems
and
animal
models
cannot
completely
recapitulate
clinical
complexity
these
humans.
Therefore,
there
is
a
dire
need
for
higher
fidelity
biological
capable
replicating
phenotypes
to
inform
outcomes
therapeutic
development.
Cardiac
tissue
engineering
(CTE)
strategies
have
emerged
fulfill
this
by
design
three-dimensional
myocardial
from
human
pluripotent
stem
cells.
In
way,
CTE
serve
as
highly
controllable
variety
applications-including
physiological
pathological
modeling,
drug
discovery
preclinical
testing
platforms,
even
direct
interventions
clinic.
Although
significant
progress
has
been
made
development
technologies,
critical
challenges
necessary
refinements
are
required
derive
more
advanced
heart
technologies.
review,
we
distill
three
focus
areas
field
address:
I)
Generating
cardiac
muscle
types
scalable
manufacturing
methods,
II)
Engineering
structure,
function,
analyses,
III)
Curating
system
specific
application.
each
our
areas,
emphasize
importance
designing
mimicking
intricate
intercellular
connectivity
discuss
fundamental
considerations
that
subsequently
arise.
We
conclude
highlighting
cutting-edge
applications
use
technologies
modeling
repair
damaged
diseased
hearts.
Bulletin of Siberian Medicine,
Год журнала:
2025,
Номер
24(1), С. 141 - 153
Опубликована: Апрель 16, 2025
Atherosclerosis
and
atherosclerosis-related
cardiovascular
diseases
are
a
significant
public
health
concern
rapidly
evolving
area
of
research
in
both
fundamental
clinical
medicine.
Despite
the
extensive
history
studying,
many
aspects
atherosclerosis
etiology
pathogenesis
remain
unclear.
Traditionally,
has
been
viewed
terms
localized
accumulation
specific
lipoprotein
fractions
arterial
wall.
However,
innate
adaptive
immunity
play
active
roles
atherogenesis.
Cells
mediators
immune
system
engage
intricate
interactions
with
cellular
extracellular
components
all
layers
vascular
For
this
reason,
scientific
community
have
reached
consensus
on
crucial
role
inflammation
onset,
progression,
destabilization
an
atherosclerotic
plaque.
Therefore,
atherogenesis
can
be
considered
not
only
as
metabolic
disorder,
but
also
immunoinflammatory
process.
The
aim
lecture
was
to
summarize
contemporary
data
regarding
at
various
stages
continuum.
Frontiers in Physiology,
Год журнала:
2025,
Номер
16
Опубликована: Май 26, 2025
Numerous
studies
over
several
decades
found
that
there
are
significant
sex
differences
in
the
development
and
severity
of
atherosclerosis,
which
include
plaque
burden,
composition
vulnerability
to
rupture.
This
review
provides
historical
analysis
these
starting
with
early
histological
post
mortem
samples
modern
high-resolution
imaging
techniques.
It
is
discussed
abundance
evidence
obtained
by
an
array
approaches
demonstrates
men
more
prone
develop
manifests
itself
earlier
initiation
plaques,
while
occurrence
accelerated
following
menopause.
These
findings
unequivocally
show
likely
plaques
larger
lipid-rich
necrotic
cores,
thinner
fibrous
caps,
stronger
inflammatory
responses,
resulting
increased
at
a
younger
age.
However,
rapid
escalation
instability
postmenopausal
women,
caused
reduction
smooth
muscle
cell
density
changes
calcification
patterns,
results
comparable
atherosclerotic
burden
women
older
adults.
highlight
how
age,
influence
atherosclerosis.
Understanding
essential
for
creating
better
ways
assess
treat
heart
disease
women.
Myocarditis
is
a
potentially
life-threatening
disorder
that
challenging
to
diagnose
and
treat.
T
cell-mediated
autoimmunity
now
recognized
as
key
mechanism
in
myocarditis.
Under
physiologic
conditions,
regulatory
cells
maintain
peripheral
tolerance
prevent
spontaneous
myocarditis
development,
but
damaged
tissue
activation
of
the
innate
immune
system
promotes
effector
cell
expansion
progression.
Our
lab
has
previously
identified
subset
memory
characterised
by
expression
hepatocyte
growth
factor
(HGF)
receptor,
cMet,
selectively
localise
inflamed
cardiac
muscle.
Further
studies
have
implicated
cMet+
mediators
acute
T-
mediated
autoimmune
myocarditis,
also
being
central
development
murine
chronic
ultimately,
dilated
cardiomyopathy
(DCM).
However,
HGF
been
shown
exert
multiple
complex
effects
on
inflammation
its
resolution.Here,
we
review
which
mediate
cMet
modulation
responses
heart.
International Journal of Cardiology Cardiovascular Risk and Prevention,
Год журнала:
2024,
Номер
22, С. 200307 - 200307
Опубликована: Июль 4, 2024
Systemic
inflammation
has
a
critical
role
in
the
development
of
symptomatic
coronary
artery
disease
(CAD).
Identification
inflammatory
pathways
may
provide
platform
for
novel
therapeutic
approaches.
We
sought
to
determine
whether
there
are
differences
circulating
cytokine
profiles
between
patients
with
CAD
and
disease-free
controls
as
well
according
severity
disease.
AJP Heart and Circulatory Physiology,
Год журнала:
2024,
Номер
327(4), С. H937 - H946
Опубликована: Авг. 16, 2024
Influenza
A
virus
(IAV)
infection
while
primarily
affecting
the
lungs,
is
often
associated
with
cardiovascular
complications.
However,
mechanisms
underlying
this
association
are
not
fully
understood.
Here,
we
investigated
potential
role
of
FBXL19,
a
member
Skp1-Cullin-1-F-box
family
E3
ubiquitin
ligase,
in
IAV-induced
cardiac
inflammation.
We
demonstrated
that
FBXL19
overexpression
endothelial
cells
(ECs)
reduced
viral
titers
and
IAV
matrix
protein
1
(M1)
levels
increasing
antiviral
gene
expression,
including
interferon
(IFN)-α,
-β,
-γ
RANTES
(regulated
on
activation
normal
T
cell
expressed
secreted)
tissue
IAV-infected
mice.
Moreover,
EC-specific
attenuated
infection-reduced
regulatory
factor
3
(IRF3)
level
without
altering
its
mRNA
suppressed
Furthermore,
triggered
cellular
senescence
programs
heart
as
indicated
by
upregulation
p16
p21
downregulation
lamin-B1
levels,
which
were
partially
reversed
ECs.
Our
findings
indicate
protects
against
damage
enhancing
interferon-mediated
signaling,
reducing
inflammation,
suppressing
programs.