The American Journal of Sports Medicine,
Journal Year:
2024,
Volume and Issue:
52(12), P. 3130 - 3146
Published: Sept. 23, 2024
Background:
Osteoarthritis
(OA)
is
a
prevalent
and
disabling
disease
that
affects
significant
proportion
of
the
global
population.
Urine-derived
stem
cells
(USCs)
have
shown
great
prospects
in
treatment
OA,
but
there
no
study
has
compared
them
with
traditional
cells.
Purpose:
This
aimed
to
compare
therapeutic
efficacy
mechanisms
USCs
adipose-derived
(ADSCs)
for
OA
treatment.
Study
Design:
Controlled
laboratory
study.
Methods:
We
biological
properties
ADSCs
using
CCK-8,
colony
formation,
EdU,
adhesion,
apoptosis
assays.
evaluated
protective
effects
on
IL-1β–treated
chondrocytes
by
chemical
staining,
immunofluorescence,
Western
blotting.
assessed
chondrocyte
autophagy
transmission
electron
microscopy,
also
intra-articular
injections
gross,
histological,
micro–computed
tomography,
immunohistochemical
analyses
an
rat
model
induced
anterior
cruciate
ligament
transection.
Results:
showed
higher
proliferation,
DNA
synthesis,
anti-apoptotic
abilities
than
ADSCs.
Both
increased
expression
cartilage-specific
proteins
decreased
matrix
degradation–related
inflammatory
factors
chondrocytes.
had
greater
advantage
suppressing
MMP-13
enhanced
chondrocytes,
being
more
effective
The
inhibitor
3-MA
reduced
Conclusion:
To
our
knowledge,
this
first
explore
knee
Considering
superior
terms
noninvasive
acquisition,
high
cost-benefit
ratio,
low
ethical
concerns,
suggests
they
may
be
promising
option
under
rigorous
regulatory
pathways.
Clinical
Relevance:
cell
source
treat
strengthens
evidence
application
USCs.
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: April 12, 2024
Abstract
The
current
first-line
treatment
for
repairing
cartilage
defects
in
clinical
practice
is
the
creation
of
microfractures
(MF)
to
stimulate
release
mesenchymal
stem
cells
(MSCs);
however,
this
method
has
many
limitations.
Recent
studies
have
found
that
MSC-derived
extracellular
vesicles
(MSC-EVs)
play
an
important
role
tissue
regeneration.
This
study
aimed
verify
whether
MSC-EVs
promote
damage
repair
mediated
by
MFs
and
explore
mechanisms.
In
vitro
experiments
showed
human
umbilical
cord
Wharton’s
jelly
(hWJMSC-EVs)
promoted
vitality
chondrocytes
proliferation
differentiation
ability
bone
marrow-derived
MSCs.
was
mainly
because
hWJMSC-EVs
carry
integrin
beta-1
(ITGB1),
MSCs
overexpress
ITGB1
after
absorbing
EVs,
thereby
activating
transforming
growth
factor-β/Smad2/3
axis.
a
rabbit
knee
joint
model
osteochondral
defect
repair,
injection
different
concentrations
into
cavity
concentration
50
µg/ml
significantly
improved
formation
transparent
MF
surgery.
Extraction
regenerated
revealed
changes
ITGB1,
factor-β,
Smad2/3
were
directly
proportional
cartilage.
summary,
Graphical
abstract
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(7), P. 2896 - 2896
Published: March 22, 2025
Links
between
cathepsin
K
and
the
pathophysiology
of
osteoarthritis
(OA)
can
be
established,
not
least
because
overabundance
in
serum
OA
patients
upregulation
degraded
cartilage
animal
models
OA.
Chondrocytes,
chondroclasts,
or
osteoclasts
contribute
to
accumulated
at
diseased
osteochondral
junction.
After
a
general
presentation
physiology,
as
well
its
degradation
processes,
we
describe
function
effect
on
via
type
II
collagen
cleavage.
An
overview
most
promising
inhibitors
is
then
presented,
together
with
their
vitro
effects.
Although
intensive
research
initially
focused
bone
resorption,
there
growing
interest
potential
these
drugs
prevent
degradation.
In
this
review,
summarize
pre-clinical
clinical
trials
that
support
use
treatment
To
date,
no
molecules
are
commercially
available,
although
few
have
undergone
trials,
but
believe
development
could
broaden
therapeutic
arsenal
for
Stem Cell Research & Therapy,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 14, 2025
Hepatic
ischemia-reperfusion
injury
(HIRI)
severely
threatens
the
success
rates
of
liver
surgery
and
transplantation.
Its
complex
pathological
process
involves
multiple
factors
such
as
oxidative
stress,
inflammatory
responses,
ferroptosis,
creating
an
urgent
need
for
new
therapeutic
strategies.
Exosomes
derived
from
mesenchymal
stem
cells
(MSCs)
are
emerging
a
next-generation
acellular
approach.
With
their
outstanding
immune-regulatory
capabilities,
significant
reparative
functions,
good
biocompatibility,
they
leading
innovations
in
field
HIRI
treatment.
This
article
provides
systematic
comparison
characteristics
MSC-derived
exosomes(MSC-EXOs)
four
different
sources:
adipose
tissue,
bone
marrow,
umbilical
cord,
induced
pluripotent
cells.
Although
clinical
translation
MSC-EXOs
still
faces
challenges
variations
isolation
methods,
large-scale
production,
safety
assessments,
remarkable
effects
vast
application
potential
signal
arrival
era
precision
treatment
HIRI.
review
not
only
comprehensive
theoretical
foundation
to
promote
but
also
opens
up
innovative
research
directions
regenerative
medicine.
The American Journal of Sports Medicine,
Journal Year:
2024,
Volume and Issue:
52(12), P. 3130 - 3146
Published: Sept. 23, 2024
Background:
Osteoarthritis
(OA)
is
a
prevalent
and
disabling
disease
that
affects
significant
proportion
of
the
global
population.
Urine-derived
stem
cells
(USCs)
have
shown
great
prospects
in
treatment
OA,
but
there
no
study
has
compared
them
with
traditional
cells.
Purpose:
This
aimed
to
compare
therapeutic
efficacy
mechanisms
USCs
adipose-derived
(ADSCs)
for
OA
treatment.
Study
Design:
Controlled
laboratory
study.
Methods:
We
biological
properties
ADSCs
using
CCK-8,
colony
formation,
EdU,
adhesion,
apoptosis
assays.
evaluated
protective
effects
on
IL-1β–treated
chondrocytes
by
chemical
staining,
immunofluorescence,
Western
blotting.
assessed
chondrocyte
autophagy
transmission
electron
microscopy,
also
intra-articular
injections
gross,
histological,
micro–computed
tomography,
immunohistochemical
analyses
an
rat
model
induced
anterior
cruciate
ligament
transection.
Results:
showed
higher
proliferation,
DNA
synthesis,
anti-apoptotic
abilities
than
ADSCs.
Both
increased
expression
cartilage-specific
proteins
decreased
matrix
degradation–related
inflammatory
factors
chondrocytes.
had
greater
advantage
suppressing
MMP-13
enhanced
chondrocytes,
being
more
effective
The
inhibitor
3-MA
reduced
Conclusion:
To
our
knowledge,
this
first
explore
knee
Considering
superior
terms
noninvasive
acquisition,
high
cost-benefit
ratio,
low
ethical
concerns,
suggests
they
may
be
promising
option
under
rigorous
regulatory
pathways.
Clinical
Relevance:
cell
source
treat
strengthens
evidence
application
USCs.