Journal of Inflammation Research,
Journal Year:
2024,
Volume and Issue:
Volume 17, P. 11137 - 11160
Published: Dec. 1, 2024
Background:The
aging
of
skin
is
a
diversified
biological
phenomenon,
influenced
by
combination
genetic
and
environmental
factors.However,
the
specific
mechanism
photoaging
not
yet
completely
elucidated.Methods:
Gene
expression
profiles
for
patients
were
obtained
from
Expression
Omnibus
(GEO)
collection.We
conducted
single-cell
intercellular
communication
investigations
to
identify
potential
gene
sets.Predictive
models
created
using
LASSO
regression.The
relationships
between
genes
immune
cells
investigated
single
sample
set
enrichment
analysis
(ssGSEA)
variance
(GSVA).The
molecular
processes
important
studied
analysis.A
miRNA
network
was
look
target
miRNAs
connected
with
genes,
transcriptional
regulation
used
related
transcription
factors.Finally,
merging
co-expression
networks
drug
prediction
shows
pathways
treatment
targets.Furthermore,
we
validated
role
key
cell
infiltration,
Adenosine
5'-monophosphate
(AMP)-activated
protein
kinase
(AMPK)
pathway
in
photoaging,
which
identified
through
bioinformatics
analysis,
vivo
reverse
quantitative
PCR
(RT-qPCR),
immunofluorescence
labeling,
Western
blotting.Results:
This
study
discovered
three
including
Atp2b1,
Plekho2,
Tspan13,
perform
crucial
functions
process.Immune
infiltration
showed
increased
M1
macrophages
CD4
memory
T
group.Further
signaling
indicated
that
these
are
enriched
multiple
metabolic
pathways.The
significant
roles
AMPK
vivo.
Conclusion:This
research
revealed
underlying
mechanisms
indicating
such
as
Atp2b1
Tspan13
play
pathways.These
findings
provide
new
theory
prospective
targets
advancement
relevant
drugs.
The Journal of Cardiovascular Aging,
Journal Year:
2025,
Volume and Issue:
5(1)
Published: Jan. 22, 2025
With
the
increase
in
life
expectancy
globally,
challenge
of
dealing
with
aging
becomes
more
prominent.
Aging
is
a
risk
factor
for
several
diseases,
including
cardiovascular
disease.
Mitochondria,
which
have
long
been
studied
relation
to
aging,
play
crucial
role
maintaining
cellular
homeostasis.
However,
there
limitation
interorganellar
communication
as
organisms
age.
The
unfolded
protein
response
mitochondria
(UPRmt)
activated
during
stress
maintain
mitochondrial
homeostasis
and
prevent
accumulation
damaged
mitochondria.
This
involves
signaling
from
nucleus,
leading
transcriptional
changes.
In
context
heart,
this
review
explores
terms
function
morphology.
It
also
discusses
impact
UPRmt
on
cardiac
diseases
such
heart
failure,
acute
myocardial
infarction,
dilated
cardiomyopathy.
highlights
potential
mitochondria-endoplasmic
reticulum
contact
sites
(MERCs)
modulating
aging.
Finally,
it
provides
an
update
molecules
that
induce
activity,
potentially
benefiting
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(6), P. 2617 - 2617
Published: March 14, 2025
This
study
comprehensively
investigated
keratinocyte
subpopulation
heterogeneity
and
developmental
trajectories
during
skin
aging
using
single-cell
sequencing,
transcriptomics,
facial
aging-related
genome-wide
association
studies
(GWAS)
data.
We
identified
three
major
subpopulations:
basal
cells
(BCs),
spinous
(SCs),
IFI27+
keratinocytes.
Single-cell
pseudotime
analysis
revealed
that
can
differentiate
along
two
distinct
paths:
toward
differentiation
or
the
inflammatory
state.
With
aging,
proportion
of
significantly
increased,
displaying
more
active
immunomodulatory
signals.
Through
cell–cell
communication
analysis,
we
found
signaling
pathways,
including
NOTCH,
PTPR,
PERIOSTIN,
exhibited
characteristics
different
branches.
Integration
GWAS
data
significant
loci
on
chromosomes
2,
3,
6,
9
were
spatially
correlated
with
key
biological
pathways
(including
antigen
processing,
oxidative
stress,
apoptosis).
These
findings
reveal
complex
cellular
molecular
mechanisms
underlying
offering
potential
targets
for
novel
diagnostic
approaches
therapeutic
interventions.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 3, 2025
Activation
of
the
STING
pathway
is
essential
for
restoring
immune
surveillance
against
dormant
disseminated
tumor
cells
(DTCs)
in
lungs.
Inhaled
Mn2+
has
potential
as
a
agonist;
however,
its
clinical
application
limited
by
risk
chronic
inflammation
and
metastasis,
primarily
due
to
reactive
oxygen
species
(ROS)
generation
during
inhalation.
To
address
these
risks,
salvianolic
acid
B
(salB)
was
identified
an
effective
ionophore
Mn2+,
enhancing
activation
while
mitigating
ROS-induced
inflammation.
In
this
study,
salB
mitigated
Mn2+-induced
ROS
levels
enhanced
signaling,
providing
safer,
noninflammatory
approach
activating
lung
DTCs.
The
salB-Mn2+
complexes
were
encapsulated
human
serum
albumin
nanoparticles
(HSA
NPs)
PET
MRI
analyses
revealed
that
intratracheal
administration
HSA
NP@salB-Mn2+
restricted
Mn2+'s
systemic
distribution,
retaining
it
lungs
minimizing
central
nervous
system
accumulation.
Subsequent
immunofluorescence
further
confirmed
effectively
targeted
metastatic
lesions.
Despite
extended
retention
tissue,
histological
analysis
showed
minimal
mice
treated
with
NP@salB-Mn2+,
contrast
those
receiving
MnCl2
or
MnO.
Consequently,
demonstrated
superior
suppression
4T1
cell
metastasis
postsurgical
relative
Mechanistically,
functions
agonist,
independently
p-STING,
which
synergizes
significantly
amplify
signaling
downstream
target
engagement.
mouse
model,
combination
αPD-1
antibody
reduced
DTC
dormancy
detection,
confirming
immunotherapeutic
potential.
These
findings
establish
promising
inhalable
treatment,
three
key
advantages:
prolonged
retention,
risk,
STING-activating
efficacy.
Periodontitis
is
an
oral
immunoinflammatory
disease,
and
macrophages
play
a
crucial
role
in
its
pathophysiology.
However,
macrophage
death
during
antibacterial
activities
will
exacerbate
inflammation
tissue
damage.
Porphyromonas
gingivalis
major
constituent
of
subgingival
biofilm
plaques
periodontitis,
but
the
effects
precise
molecular
mechanisms
by
which
it
triggers
remain
unknown.
Here
we
found
that
P.
infection
notably
activated
multiple
pathways
bone-marrow-derived
macrophages,
including
pyroptosis,
apoptosis
necrosis.
Furthermore,
using
RNA
sequencing,
identified
markedly
increased
expression
Z-DNA
binding
protein
1
(Zbp1)
macrophages.
Initially
as
interferon-induced
tumor-associated
protein,
Zbp1
serves
upstream
sensor
regulates
cell
activating
PANoptosis.
Mechanistically,
induced
mitochondrial
stress
response,
prompting
release
DNA.
This
DNA
then
interacted
with
Zbp1,
consequently
augmenting
downstream
PANoptosis
signals.
In
addition,
stimulated
through
Tlr2/4-JNK-Stat3/5
pathway,
exacerbating
death.
Importantly,
blocking
biosynthesis
endogenous
pharmacological
delivery
microneedles
improved
survival
gingivalis-infected
inhibited
periodontal
destruction.
These
findings
highlight
potential
therapeutic
target
for
gingivalis-induced
periodontitis.
Experimental Dermatology,
Journal Year:
2025,
Volume and Issue:
34(5)
Published: May 1, 2025
ABSTRACT
Ultraviolet
radiation
(UVR)
is
the
most
detrimental
external
factor
that
induces
acute
photodamage,
photoaging
and
skin
cancers,
with
complex
underlying
molecular
mechanisms
initiated
mainly
by
increased
DNA
damage
reactive
oxygen
species
(ROS)
generation.
Mitochondria
are
main
organelles
in
cells
produce
ROS
energy
regulate
various
physiological
pathological
signalling
pathways.
Continuous
UVR
on
human
can
induce
mitochondrial
mutations
excessive
production,
creating
feedback
between
each
other
subsequently
causing
a
reduction
membrane
potential
(MMP)
respiratory
capacity.
Deficiencies
function
apoptosis,
mitophagy
senescence,
resulting
UVR‐induced
photodamage
photoaging.
Mitochondrial
biogenesis
metabolic
pathways
play
critical
roles
progression
of
particularly
melanoma,
which
malignant
infrequent
type
cancer.
In
this
review,
we
describe
recent
advances
determining
intimate
relationship
damage,
suggesting
candidates
novel
chemical/natural
components
to
protect
from
cancers
via
targeting
mechanisms.
Polymers for Advanced Technologies,
Journal Year:
2025,
Volume and Issue:
36(5)
Published: May 1, 2025
ABSTRACT
Periodontitis
is
an
immune‐reactive
disease
characterized
by
excessive
inflammation
and
oxidative
stress
(OS).
Salvianolic
acid
B
(Sal
B)
a
component
isolated
from
the
root
of
Salvia
miltiorrhiza
,
known
for
its
strong
anti‐inflammatory
antioxidant
effects.
Our
study
examined
beneficial
effects
Sal
on
OS
mitochondrial
function
(MF)
in
periodontitis,
as
well
potential
mechanisms.
In
vitro
experiments
demonstrated
that
can
reduce
inflammatory
response
periodontal
tissue
cells
eliminate
products
such
reactive
oxygen
species
(ROS).
Furthermore,
enhances
membrane
(MMP)
increases
adenosine
triphosphate
(ATP)
production.
We
designed
methacryloylated
glycol
chitosan/β‐glycerophosphate
composite
hydrogel
(MAGC/β‐GP
Gel)
localized
delivery
B.
B@MAGC/β‐GP
gel
stable
exhibits
good
thermal
sensitivity,
allowing
continuous
release
pocket.
Results
mouse
model
periodontitis
showed
significantly
reduces
alveolar
bone
absorption,
eliminates
ROS,
MMP
levels,
alleviates
inflammation.
Overall,
this
demonstrates
has
therapeutic
agent
novel
material
expected
to
be
used
intrapocket
injections
clinical
settings.
Molecules,
Journal Year:
2024,
Volume and Issue:
29(17), P. 4060 - 4060
Published: Aug. 27, 2024
Extended
exposure
to
UVB
(280-315
nm)
radiation
results
in
oxidative
damage
and
inflammation
of
the
skin.
Previous
research
has
demonstrated
that
pilose
antler
extracts
have
strong
anti-inflammatory
properties
possess
antioxidant
effects.
This
study
aimed
elucidate
mechanism
protein
repairing
photodamage
caused
by
HaCaT
cells
ICR
mice.
Pilose
(PAP)
was
found
increase
expression
type
I
collagen
hyaluronic
acid
under
irradiation
while
also
inhibiting
reactive
oxygen
species
(ROS)
production
stress
vitro.
In
vivo,
topical
application
effectively
attenuated
UVB-induced
skin
mice
reducing
interleukin-1β
(IL-β),
interleukin-6
(IL-6),
tumor
necrosis
factor-α
(TNF-α)
alleviating
stress.
It
shown
repaired
through
MAPK
TGF-β/Smad
pathways.