The association of TNF-alpha secretion and mtDNA copy number in CD14+ monocytes of patients with obesity and CHD
Frontiers in Molecular Biosciences,
Journal Year:
2024,
Volume and Issue:
11
Published: March 20, 2024
Introduction
Mitochondrial
dysfunction
may
be
one
of
the
causes
inflammatory
activation
monocytes
and
macrophages,
which
leads
to
excessive
secretion
mediators
development
chronic
inflammation.
Aims
The
study
was
aimed
evaluate
cytokine
tumor
necrosis
factor-α
(TNF-α)
in
primary
culture
monocytes,
analyze
its
relationship
with
number
mitochondrial
DNA
(mtDNA)
copies
blood
patients
coronary
heart
disease
(CHD)
obesity.
Materials
methods
108
obesity
concomitant
CHD
a
control
group
25
participants
were
included
study.
CD14
+
isolated
by
standard
method
ficoll-urographin
gradient,
followed
separation
using
magnetic
particles.
mtDNA
estimated
qPCR.
Results
It
demonstrated
that
significantly
increased
groups
comparison
group.
copy
positively
correlated
basal
LPS-stimulated
TNF-α
secretion,
most
significant
correlation
found
Conclusion
Thus,
change
indicates
presence
dysfunction,
confirm
direct
involvement
mitochondria
violation
response
revealed
this
as
an
TNF-α.
Language: Английский
RNA sequencing analysis of early-stage atherosclerosis in vascular-on-a-chip and its application for comparing combustible cigarettes with heated tobacco products
Kazuhiro �Ohashi,
No information about this author
Ayaka Hayashida,
No information about this author
Atsuko Nozawa
No information about this author
et al.
Current Research in Toxicology,
Journal Year:
2024,
Volume and Issue:
6, P. 100163 - 100163
Published: Jan. 1, 2024
Our
previous
study
showed
promising
results
in
replicating
early-stage
atherosclerosis
when
vascular
endothelial
cells
(VECs)
were
exposed
to
cigarette
smoke
(CS)
extract
via
M0
macrophages.
We
used
an
organ-on-a-chip
system
as
alternative
animal
testing
model
atherosclerosis,
which
is
a
complex
disease
involving
and
immune
cell
communications.
By
incorporating
macrophages
into
the
vascular-on-a-chip
system,
we
aimed
mimic
indirect
effects
of
inhalable
substances,
such
CS,
on
VECs.
In
current
study,
further
examined
suitability
our
Language: Английский
Exploring the Association of Biochemical Characterization and Genetic Determinants of TNF-α, CXCR2, and CCR5 Delta 32 Mutation with Predisposition to Polycystic Ovary Syndrome
Kholoud S. Almasoudi,
No information about this author
Eram Hussain,
No information about this author
Reema Almotairi
No information about this author
et al.
Life,
Journal Year:
2024,
Volume and Issue:
14(8), P. 949 - 949
Published: July 28, 2024
PCOS
is
a
heterogeneous,
multifactorial
endocrine
disorder
with
complex
pathophysiology.
It
globally
rising
infertility
that
affects
large
percentage
of
women
reproductive
age,
relatively
high
prevalence
8–13%.
Genome-wide
association
studies
have
revealed
associations
genetic
variations
many
diseases,
including
PCOS.
The
cellular
activity
IL8
mediated
by
the
receptor
CXCR2,
and
transcription
controlled
TNF-α.
Therefore,
this
study
aimed
to
investigate
TNF-α,
CCR5-delta32,
CXCR2
gene
Methodology:
In
case
control
study,
we
used
amplification-refractory
mutation
system
(ARMS)-PCR
detect
determine
presence
polymorphic
variants
in
subjects.
These
polymorphs
may
serve
as
critical
candidate
pathogenesis
therapeutics.
Results:
case–control
study’s
findings
majority
biochemical
serum
biomarkers
examined
investigation—including
lipids
(LDL,
HDL,
cholesterol),
T2DM
markers
(fasting
glucose,
free
insulin,
HOMA-IR),
hormones
(FSH,
LH,
testosterone,
progesterone)—exhibited
statistically
significant
changes
patients.
distributions
TNF-α
(rs1800629),
(rs2230054)
genotypes
analyzed
within
patients
healthy
controls
considered
population
were
(p
<
0.05).
heterozygosity
CXCR2-CA,
GA,
CCR5(WT+Δ32*)
was
significantly
associated
susceptibility,
OR
p
0.05
codominant
model.
Similarly,
A
allele
genes,
along
CCR5Δ32*(mutant)
allele,
0.05.
Likewise,
(CA+AA)
vs
CC
genotype
increased
susceptibility
PCOS,
2.25,
0.032.
Conclusions:
Our
concludes
rs1800629G>A,
CXCR2-rs2230054C>T,
CCR5-Delta32
rs333
are
potential
loci
for
developing
Tabuk
population.
might
eventually
be
useful
identifying
classifying
those
who
at
risk
To
validate
these
results,
it
advised
further
longitudinal
conducted
diverse
ethnic
populations
larger
sample
sizes.
Language: Английский