Drug Design Development and Therapy,
Journal Year:
2025,
Volume and Issue:
Volume 19, P. 457 - 469
Published: Jan. 1, 2025
Exosomes,
small
extracellular
vesicles
secreted
by
various
cells,
play
crucial
roles
in
the
pathogenesis
and
treatment
of
oral
diseases.
Recent
studies
have
highlighted
their
involvement
orthodontics,
periodontitis,
squamous
cell
carcinoma
(OSCC),
hand,
foot,
mouth
disease
(HFMD).
Exosomes
a
positive
effect
on
inflammatory
environment
cavity,
remodeling
regeneration
tissues,
offer
promising
therapeutic
options
for
bone
periodontal
tissue
restoration.
In
OSCC
tumor-derived
exosomes
promote
cancer
progression
through
proliferation,
migration,
invasion,
angiogenesis,
serve
as
potential
biomarkers
early
diagnosis
prognosis.
Additionally,
engineered
constructed
specifically
based
exosome
properties
hold
great
promise
targeted
drug
delivery
regenerative
therapies
such
orthodontics
healing.
With
continued
research,
improving
diseases,
advancing
personalized
therapies.
Journal of Inflammation Research,
Journal Year:
2025,
Volume and Issue:
Volume 18, P. 1317 - 1331
Published: Jan. 1, 2025
Periodontitis
is
a
prevalent
yet
frequently
overlooked
oral
disease
that
linked
to
range
of
systemic
conditions.
Although
basic
treatment
and
periodontal
surgery
can
alleviate
the
symptoms
periodontitis
certain
extent,
severe
tissue
defects
or
refractory
cases
not
effective.
Extracellular
vesicles
(EVs)
are
subcellular
lipid
bilayer
particles
come
from
variety
sources
in
biological
fluids
vertebrates.
They
play
key
role
intercellular
communication
by
transporting
multiple
signaling
molecules.
Recent
research
has
indicated
EVs
derived
pathogens
trigger
periodontitis,
exacerbate
damage,
potentially
disseminate
other
parts
body,
leading
Conversely,
extracellular
dental
stem
cells
(DSCs)
have
demonstrated
ability
regulate
local
immune
environment
foster
regeneration
repair
tissues,
positioning
them
as
promising
candidate
for
cell-free
therapeutic
approaches
periodontitis.
This
review
aims
summarize
latest
on
involvement
different
pathogenesis
especially
systematically
elucidate
mechanism
secreted
periodontitis-related
diseases
first
time.
By
uncovering
these
complex
regulatory
processes,
new
more
effective
be
explored
battle
against
its
associated
diseases.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 10, 2025
Abstract
Background
The
causal
relationship
between
inflammatory
bowel
disease
(IBD)
and
periodontitis
remains
a
topic
of
debate.
This
study
aimed
to
assess
the
two.
Methods
employed
bidirectional
Mendelian
randomization
(MR)
analysis
combined
with
integrated
bioinformatics.
On
one
hand,
it
explored
IBD
using
MR
analysis,
inverse
variance
weighting
(IVW)
as
judgment
basis
conducted
sensitivity
analysis.
other
utilized
RNA
sequencing
data
mine
co-expressed
differential
genes
two
diseases,
explore
common
molecules
potential
molecular
signaling
pathways
them.
Results
found
link
(P
<
0.05),
showing
consistency
no
significant
heterogeneity
or
pleiotropy
>
0.05).
results
further
confirmed
bioinformatics
indicated
that
immune-related
factors,
represented
by
IL1B
CXCR4,
pathways,
notably
TNF
IL17,
may
play
an
important
role
in
progression
both
diseases.
Conclusion
study,
through
Randomization
established
mutual
periodontitis.
transcriptome
revealed
pathological
mechanisms
key
immune
regulatory
factors
these
These
findings
provide
scientific
for
diagnosis
treatment
periodontitis,
emphasizing
importance
deep
understanding
interaction
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(2), P. 476 - 476
Published: Feb. 15, 2025
Background/Objectives:
A
bidirectional
association
between
inflammatory
bowel
disease
(IBD)
and
periodontitis
has
been
observed,
yet
their
causal
relationship
remains
unclear.
This
study
aimed
to
investigate
the
potential
links
these
two
conditions
through
comprehensive
genetic
molecular
analyses.
Methods:
We
conducted
a
Mendelian
randomization
(MR)
analysis
integrated
with
bioinformatics
approaches.
The
relationships
were
primarily
evaluated
using
inverse
variance
weighting
(IVW),
complemented
by
multiple
sensitivity
analyses
assess
robustness
of
findings.
Additionally,
we
performed
differential
gene
expression
RNA
sequencing
data
identify
co-expressed
genes
shared
mediators
IBD
periodontitis,
followed
pathway
enrichment
analysis.
Results:
Bidirectional
MR
revealed
significant
associations
(p-value
<
0.05).
Sensitivity
demonstrated
consistency
findings,
no
evidence
heterogeneity
or
horizontal
pleiotropy
>
Integrated
identified
key
immune
regulators,
particularly
interleukin
1
beta
(IL1B)
C-X-C
motif
chemokine
receptor
4
(CXCR4),
signaling
pathways,
including
tumor
necrosis
factor
(TNF-α)
17
(IL17),
as
mechanisms
underlying
conditions.
Conclusions:
Our
findings
provide
supporting
periodontitis.
Transcriptomic
pathological
crucial
regulatory
factors
common
both
diseases.
These
insights
enhance
our
understanding
interplay
potentially
informing
new
therapeutic
strategies
for
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Based
on
observations
that
HIV-1
envelope
(Env)
proteins
the
surfaces
of
cells
have
capacity
to
fuse
with
neighboring
or
enveloped
viruses
express
CD4
receptors
and
CXCR4
co-receptors,
we
tested
factors
affect
capacities
lentiviral
vectors
pseudotyped
variants
infect
Env-expressing
cells.
The
process,
which
refer
as
fusion
in
reverse,
involves
binding
activation
cellular
Env
membranes
lentiviruses
carrying
proteins.
We
found
infection
via
reverse
depends
cell
surface
levels,
is
inhibitable
by
an
HIV-1-specific
inhibitor,
preferentially
requires
pseudotyping
a
glycosylphosphatidylinositol
(GPI)
anchored
variant,
cytoplasmic
tail-truncated
protein.
demonstrated
latently
HIV-1-infected
can
be
specifically
infected
using
this
mechanism,
increases
efficiency.
approach
allowed
us
characterize
how
alteration
plus
lipid
affected
protein
activities.
In
particular,
perturbation
membrane
cholesterol
levels
did
not
activity.
contrast,
assembled
deficient
for
long
chain
sphingolipids
showed
increased
infectivities,
while
incorporated
scramblase
were
non-infectious.
Our
results
yield
new
insights
influence
functions.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(4), P. 472 - 472
Published: March 26, 2025
Based
on
observations
that
HIV-1
envelope
(Env)
proteins
the
surfaces
of
cells
have
capacity
to
fuse
with
neighboring
or
enveloped
viruses
express
CD4
receptors
and
CXCR4
co-receptors,
we
tested
factors
affect
capacities
lentiviral
vectors
pseudotyped
variants
infect
Env-expressing
cells.
The
process,
which
refer
as
fusion
in
reverse,
involves
binding
activation
cellular
Env
membranes
lentiviruses
carrying
proteins.
We
found
infection
via
reverse
depends
cell
surface
levels,
is
inhibitable
by
an
HIV-1-specific
inhibitor,
preferentially
requires
pseudotyping
a
glycosylphosphatidylinositol
(GPI)-anchored
variant
cytoplasmic
tail-truncated
protein.
demonstrated
latently
HIV-1-infected
can
be
specifically
infected
using
this
mechanism,
increases
efficiency.
approach
allowed
us
characterize
how
alteration
plus
lipid
affected
protein
activities.
In
particular,
perturbation
membrane
cholesterol
levels
did
not
activity.
contrast,
assembled
deficient
for
long-chain
sphingolipids
showed
increased
infectivities,
while
incorporated
scramblase
were
non-infectious.
Our
results
yield
new
insights
into
influence
functions.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: March 26, 2025
Graft-versus-host
disease
(GvHD)
is
a
prevalent
complication
following
allogeneic
hematopoietic
stem
cell
transplantation
(HSCT)
and
characterized
by
relatively
high
morbidity
mortality
rates.
GvHD
can
result
in
extensive
systemic
damage
patients
HSCT
(allo-HSCT),
with
the
skin,
gastrointestinal
tract,
liver
frequently
being
primary
target
organs
affected.
The
severe
manifestations
of
acute
intestinal
often
indicate
poor
prognosis
for
after
allo-HSCT.
Endoscopy
histopathological
evaluation
remain
employed
to
diagnose
GvHD,
auxiliary
examinations
exclude
differential
diagnoses.
Currently,
reliable
serum
biomarkers
diagnosis
are
scarce.
As
an
essential
part
standard
transplant
protocols,
early
application
immunosuppressive
drugs
effectively
prevents
GvHD.
Among
them,
steroids
represent
first-line
therapeutic
agents,
JAK2
inhibitor
ruxolitinib
represents
second-line
agent.
no
efficacious
treatment
modality
exists
steroid-resistant
aGvHD.
Therefore,
still
face
significant
medical
demands.
Extracellular
vesicles
(EVs)
nanometer
micrometer-scale
biomembrane
containing
various
bioactive
components,
such
as
proteins,
nucleotides,
metabolites.
Distinctive
changes
serum-derived
EV
components
occur
allo-HSCT;
Hence,
EVs
expected
be
potential
diagnosing
treating
Furthermore,
cell-free
therapeutics
derived
from
mesenchymal
cells
(MSCs)
have
manifested
remarkable
efficacy
preclinical
models
trials
Customized
engineered
fewer
toxic
side
effects
combined
hold
broad
prospects
clinical
translation.
This
review
article
examines
value
translating
into
applications
It
summarizes
latest
advancements
applying