Mesenchymal Stem Cell Treatment for Peripheral Nerve Injuries
Yue Wu,
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Ruijie Lu,
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Hongtao Yin
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et al.
Journal of Cellular Physiology,
Journal Year:
2025,
Volume and Issue:
240(4)
Published: April 1, 2025
ABSTRACT
Peripheral
nerve
injuries
(PNI)
affect
hundreds
of
thousands
patients
annually,
often
leading
to
life‐altering
consequences
such
as
significant
impairments
in
motor
function
and
sensory
perception.
In
recent
years,
a
growing
body
evidence
indicates
that
mesenchymal
stem
cell
(MSC)
treatment
could
complement
traditional
improve
therapeutic
outcomes
for
these
injuries.
This
paper
reviews
emerging
insights
into
the
potential
benefits
MSC
PNI
summarizes
selected
examples
interactions
between
MSCs,
peripheral
nerves,
their
microenvironment,
which
have
advanced
our
understanding
pathophysiology
MSC‐based
therapy.
We
believe
this
rapidly
moving
field
holds
great
promise
future
advancements,
guiding
rational
design
safe
effective
treatments
with
PNI.
Language: Английский
The influence of cell source on the senescence of human mesenchymal stem/stromal cells
Human Cell,
Journal Year:
2025,
Volume and Issue:
38(3)
Published: April 12, 2025
Language: Английский
Definition of Synovial Mesenchymal Stem Cells for Meniscus Regeneration by the Mechanism of Action and General Amp1200 Gene Expression
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(19), P. 10510 - 10510
Published: Sept. 29, 2024
The
quality
control
(QC)
of
pharmaceutical-grade
cell-therapy
products,
such
as
mesenchymal
stem
cells
(MSCs),
is
challenging.
Attempts
to
develop
products
have
been
hampered
by
difficulties
defining
cell-type-specific
characteristics
and
therapeutic
mechanisms
action
(MoAs).
Although
we
developed
a
cell
therapy
product,
FF-31501,
consisting
human
synovial
MSCs
(SyMSCs),
it
was
difficult
find
specific
markers
for
SyMSCs
define
the
separately
from
other
MSCs.
purpose
this
study
create
method
identifying
tissue-derived
delve
deeper
into
mechanism
SyMSC-induced
meniscus
regeneration.
Specifically,
cell-type-dependent
approach,
constructed
set
1143
genes
(Amp1200)
reported
be
associated
with
established
evaluate
them
correlating
gene
expression
patterns.
As
result,
possible
non-MSCs.
In
addition,
analysis
also
highlighted
TNSF-15.
in
vivo
rat
model
injury
found
TNSF-15
an
essential
molecule
regeneration
via
SyMSC
administration.
This
previously
MoA
molecules
allowed
MoA-dependent
approach
SyMSCs.
Therefore,
were
defined
means
two
approaches:
separate
identification
molecules.
These
approaches
would
useful
QC
products.
Language: Английский