International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(24), С. 17484 - 17484
Опубликована: Дек. 14, 2023
Mesenchymal
stem
cells
(MSCs)
are
a
promising
cell
source
for
therapy
of
intractable
diseases
in
veterinary
medicine,
but
donor-dependent
cellular
heterogeneity
is
an
issue
that
influences
therapeutic
efficacy.
Thus,
we
previously
established
immortalized
maintain
the
fundamental
properties
primary
cells,
functional
evaluation
had
not
been
performed.
Therefore,
evaluated
immunomodulatory
capacity
canine
adipose-derived
MSCs
(cADSCs)
vitro
and
vivo
to
investigate
whether
they
functions.
C57BL/6J
mice
were
treated
with
dextran
sulfate
sodium
(DSS)
induce
colitis,
injected
intraperitoneally
or
cADSCs
on
day
2
DSS
treatment,
observed
10
days.
Administration
improved
body
weight
loss
disease
activity
index
(DAI)
DSS-induced
colitic
by
shifting
peritoneal
macrophage
polarity
from
M1
M2
phenotype,
suppressing
T
helper
(Th)
1/Th17
responses
inducing
regulatory
(Treg)
cells.
They
also
inhibited
proliferation
mouse
vitro.
These
effects
comparable
results
highlight
feasibility
our
as
stable
efficacy
because
Current Issues in Molecular Biology,
Год журнала:
2025,
Номер
47(4), С. 231 - 231
Опубликована: Март 27, 2025
Mesenchymal
stromal
cells
(MSCs)
influence
tumor
biology
and
immunology
by
releasing
cytokines,
chemokines
growth
factors.
Currently,
cisplatin
is
an
integral
part
of
drug-based
therapy,
for
example,
in
head
neck
squamous
cell
carcinoma
(HNSCC).
Cisplatin
treatment
induces
apoptosis
as
a
primary
mechanism
action;
however,
additional
immunomodulatory
effects
are
gaining
interest.
The
aim
this
study
to
evaluate
the
possible
human
MSCs
(hMSCs).
MSCs,
obtained
from
bone
marrow,
were
characterized
analyzing
plastic
adherence,
typical
surface
features,
ability
differentiate.
Toxicity
analysis
cisplatin’s
on
including
determination
subtoxic
concentration,
was
performed
using
MTT
assay.
Enzyme-linked
immunosorbent
assays
(ELISA)
quantitative
real-time
polymerase
chain
reaction
(qRT-PCR)
used
identify
potentially
Additionally,
scratch
assay
migration.
First,
concentrations
determined.
A
significantly
reduced
protein
expression
indoleamine
2,3-dioxygenase
1
(IDO1)
under
demonstrated.
Similarly,
IL-6
qualitatively
at
concentrations,
although
without
statistical
significance.
At
mRNA
level,
qRT-PCR
showed
non-significant,
concentration-dependent
reduction
both
IDO1.
no
statistically
significant
migration
after
treatment.
In
there
tendency
decrease
IDO1
level
exposure.
These
congruent
with
each
other
dose-dependent.
This
indicates
that
not
only
acts
via
known
cytotoxic
effect,
but
may
induce
tumor-supporting
proteins,
like
IDO1,
microenvironment
concentrations.
Traditional
cytostatic
compounds,
which
can
favorably
modulate
immune
system
microenvironment,
open
new
avenues
explore
strategies
specifically
targeting
immunomodulation.
Overall,
results
indicate
beneficial
immunomodulation
cisplatin.
Frontiers in Cell and Developmental Biology,
Год журнала:
2024,
Номер
12
Опубликована: Май 31, 2024
Mesenchymal
stromal/stem
cells
(MSCs)
are
a
heterogeneous
population
of
multipotent
that
can
be
obtained
from
various
tissues,
such
as
dental
pulp,
adipose
tissue,
bone
marrow
and
placenta.
MSCs
have
gained
importance
in
the
field
regenerative
medicine
because
their
promising
role
cell
therapy
regulatory
abilities
tissue
repair
regeneration.
However,
better
characterization
these
products
is
necessary
to
further
potentiate
clinical
application.
In
this
study,
we
used
unbiased
high-resolution
mass
spectrometry-based
proteomic
analysis
investigate
impact
distinct
priming
strategies,
hypoxia
IFN-γ
treatment,
on
composition
therapeutic
functionality
secretome
produced
by
derived
amniotic
membrane
human
placenta
(hAMSCs).
Our
investigation
revealed
both
types
improved
efficacy
hAMSCs,
improvements
were
related
secretion
functional
factors
present
conditioned
medium
(CM)
exosomes
(EXOs),
which
play
crucial
roles
mediating
paracrine
effects
MSCs.
particular,
was
able
induce
pro-angiogenic,
innate
immune
response-activating,
tissue-regenerative
hAMSC
phenotype,
highlighted
elevated
production
VEGFA,
PDGFRB,
ANGPTL4,
ENG,
GRO-γ,
IL8,
GRO-α.
priming,
instead,
led
an
immunosuppressive
profile
indicated
increased
levels
TGFB1,
ANXA1,
THBS1,
HOMER2,
GRN,
TOLLIP
MCP-1.
Functional
assays
validated
angiogenic
properties
hypoxic
hAMSCs
enhanced
activity
IFN-γ-treated
hAMSCs.
This
study
extends
beyond
direct
demonstrating
influence
characteristics
hAMSC-derived
secretomes,
which,
turn,
orchestrate
peripheral
blood
cells.
research
provides
valuable
insights
into
optimization
MSC-based
therapies
systematically
assessing
comparing
type-specific
features
These
findings
highlight
new
strategies
for
enhancing
MSCs,
particularly
context
multifactorial
diseases,
paving
way
use
practice.
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Март 6, 2025
Mesenchymal
stem
cells
(MSCs)
represent
the
most
commonly
utilized
type
of
cell
in
clinical
applications.
However,
variability
quality
and
quantity
between
different
tissue
sources
donors
presents
a
significant
challenge
to
their
use.
Induced
pluripotent
(iPSCs)
are
promising
abundant
alternative
source
MSCs,
offering
potential
solution
limitations
adult
MSCs.
Nevertheless,
standardized
protocol
for
differentiation
iPSCs
into
iPSC-derived
mesenchymal
(iMSCs)
has
yet
be
established,
as
existing
methods
vary
significantly
terms
complexity,
duration,
outcome.
Many
straightforward
induce
by
culturing
MSC
media
which
supplemented
with
fetal
bovine
serum
(FBS)
or
human
platelet
lysate
(hPL),
followed
selection
MSC-like
passaging.
our
hands,
this
approach
yielded
inconsistent
iMSCs,
particularly
osteogenic
premature
senescence.
This
study
examines
impact
selective
TGF-β
inhibitor
SB431542
on
iMSC
differentiation,
demonstrating
that
inhibition
enhances
reduces
Additionally,
we
present
reliable,
xeno-free
method
producing
high-quality
iMSCs
can
adapted
Good
Manufacturing
Practice
(GMP)
compliance,
thus
enhancing
Regenerative medicine reports .,
Год журнала:
2025,
Номер
2(2), С. 53 - 60
Опубликована: Апрель 8, 2025
Allogeneic
hematopoietic
stem
cell
transplantation
is
a
highly
effective
cell-based
therapy,
but
graft-versus-host
disease
remains
major
post-transplant
complication.
While
first-line
treatment
involves
high-dose
corticosteroids,
up
to
half
of
patients
go
on
develop
steroid-refractory
disease,
where
symptoms
persist
or
worsen
despite
steroid
treatment.
This
review
provides
an
update
the
clinical
and
molecular
landscapes
examining
challenges
in
diagnosis,
management,
general
understanding
pathophysiology.
Progression
confers
poor
prognosis
associated
with
increased
morbidity.
There
are
multiple
mechanisms
that
drive
which
include
overactivation
T-cell
B-cell
mechanisms,
heightened
inflammatory
state,
cell-intrinsic
factors
mediate
responses.
Current
options
beyond
corticosteroids
JAK
pathway
inhibition,
mesenchymal
extracorporeal
photopheresis,
additional
therapies
currently
under
investigation
trials.
Potential
avenues
for
future
directions
must
aim
improve
patient
outcomes
survivorship.
Through
comprehensive
elucidation
underlying
development
mechanism-based,
regenerative
medicine-targeted
therapeutic
strategies,
optimization
trial
design,
it
anticipated
quality
life
will
be
significantly
improved.
From
standpoint,
these
advancements
expected
catalyze
transition
from
empirical
more
personalized,
mechanism-directed
therapies,
ultimately
providing
durable
disease.
Journal of Clinical Oncology,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 15, 2025
PURPOSE
The
aim
of
this
open-label,
multicenter,
randomized
controlled
trial
was
to
determine
the
efficacy
and
safety
sequential
umbilical
cord–derived
mesenchymal
stem
cell
(UC-MSC)
infusion
for
graft-versus-host
disease
(GVHD)
prevention
within
3
months
haploidentical
hematopoietic
transplantation
(haplo-HSCT).
METHODS
This
open-label
study
evaluated
UC-MSC
(administer
1
×
10
6
/kg
4
hours
before
commencement
day
0,
once
weekly
first
month
after
transplantation,
every
2
weeks
second
month,
during
third
totaling
eight
doses).
primary
end
point
2-year
cumulative
incidence
severe
chronic
GVHD
(cGVHD).
RESULTS
In
analysis,
192
qualified
participants
between
age
18
60
years
with
haplo-HSCT
in
three
transplant
centers
China
were
enrolled
randomly
assigned
MSC
control
groups.
estimated
cGVHD
all
grades
lower
group
than
(
P
=
.033
.022).
grade
4,
acute
(aGVHD)
patients
significantly
decreased
(all
<
.001).
3-year
GVHD-free
relapse-free
survival
(GRFS)
rate
62.4%,
which
higher
that
(32.0%,
hazard
ratio
[HR],
0.34,
did
not
influence
relapse
.34)
nonrelapse
mortality
.45).
CONCLUSION
Our
findings
suggest
MSCs
reduced
both
severity
aGVHD,
manifesting
as
a
better
GRFS
patients.