Stem Cell Research & Therapy,
Год журнала:
2024,
Номер
15(1)
Опубликована: Фев. 2, 2024
Abstract
Background
Spinal
cord
injuries
(SCI)
lead
to
functional
alteration
with
important
consequences
such
as
motor
and
sensory
disorders.
The
repair
strategies
developed
date
remain
ineffective.
adipose
tissue-derived
stromal
vascular
fraction
(SVF)
is
composed
of
a
cocktail
cells
trophic,
pro-angiogenic
immunomodulatory
effects.
Numerous
therapeutic
benefits
were
shown
for
tissue
reconstitution,
peripheral
neuropathy
the
improvement
neurodegenerative
diseases.
Here,
efficacy
SVF
on
sensorimotor
recovery
after
an
acute
thoracic
spinal
contusion
in
adult
rats
was
determined.
Method
Male
Sprague
Dawley
(
n
=
45)
divided
into
3
groups:
SHAM
(without
SCI
treatment),
NaCl
(animals
lesion
receiving
saline
injection
through
dura
mater)
fat
removed
from
adipocytes
mater).
Some
animals
sacrificed
14
days
start
experiment
determine
inflammatory
reaction
by
measuring
interleukin-1β,
interleukin-6
Tumor
Necrosis
Factor-α
area.
Other
followed
once
week
12
weeks
assess
(postural
locomotor
activities,
coordination).
At
end
this
period,
reflexivity
(rate-dependent
depression
H-reflex)
physiological
adjustments
(ventilatory
response
metabosensitive
muscle
activation
following
fatigue)
measured
electrophysiological
tools.
Results
Compared
non-treated
animals,
results
indicated
that
reduced
endogenous
inflammation
increased
behavioral
treated
animals.
Moreover,
H-reflex
ventilatory
fatigue
found
be
comparable
between
groups.
Conclusion
Our
highlight
effectiveness
its
high
potential
improve
functions
restore
segmental
loop
communication
supra-
sub-lesional
regions
traumatic
contusion.
Graphical
Abstract
A
short
peptide
termed
NEMO‐binding
domain
(NBD)
has
an
inhibitory
effect
on
nuclear
factor
kappa‐B
(NF‐κB).
Despite
its
efficacy
in
inhibiting
inflammatory
responses,
the
precise
neuroprotective
mechanisms
of
NBD
spinal
cord
injury
(SCI)
remain
unclear.
This
study
aims
to
determine
whether
pyroptosis‐related
aspects
involved
effects
post‐SCI.Using
RNA
sequencing,
molecular
SCI
are
explored.
The
evaluation
functional
recovery
is
performed
using
Basso
mouse
scale,
Nissl
staining,
footprint
analysis,
Masson's
trichrome
and
HE
staining.
Western
blotting,
enzyme‐linked
immunosorbent
assays,
immunofluorescence
assays
used
examine
pyroptosis,
autophagy,
lysosomal
membrane
permeabilization
(LMP),
acid
sphingomyelinase
(ASMase),
NF‐κB/p38‐MAPK
related
signaling
pathway.NBD
mitigated
glial
scar
formation,
reduced
motor
neuron
death,
enhanced
mice.
Additionally,
inhibits
ameliorate
LMP‐induced
autophagy
flux
disorder
post‐SCI.
Mechanistically,
alleviates
LMP
subsequently
enhances
by
ASMase
through
NF‐κB/p38‐MAPK/Elk‐1/Egr‐1
cascade,
thereby
mitigating
neuronal
death.
contributes
restoration
suppressing
ASMase‐mediated
depression,
pyroptosis
following
SCI,
which
may
have
potential
clinical
application
value.
Cells,
Год журнала:
2022,
Номер
12(1), С. 120 - 120
Опубликована: Дек. 28, 2022
Spinal
Cord
Injury
(SCI)
is
a
common
neurological
disorder
with
devastating
psychical
and
psychosocial
sequelae.
The
majority
of
patients
after
SCI
suffer
from
permanent
disability
caused
by
motor
dysfunction,
impaired
sensation,
neuropathic
pain,
spasticity
as
well
urinary
complications,
small
number
experience
complete
recovery.
Current
standard
treatment
modalities
the
aim
to
prevent
secondary
injury
provide
limited
recovery
lost
functions.
Stem
Cell
Therapy
(SCT)
represents
an
emerging
approach
using
differentiation,
paracrine,
self-renewal
capabilities
stem
cells
regenerate
injured
spinal
cord.
To
date,
multipotent
including
mesenchymal
(MSCs),
neural
(NSCs),
hematopoietic
(HSCs)
represent
most
investigated
types
for
in
preclinical
clinical
studies.
microenvironment
has
significant
impact
on
survival,
proliferation,
differentiation
transplanted
cells.
Therefore,
deep
understanding
pathophysiology
molecular
mechanisms
through
which
act
may
help
improve
efficacy
SCT
find
new
therapeutic
approaches
such
stem-cell-derived
exosomes,
gene-modified
cells,
scaffolds,
nanomaterials.
In
this
literature
review,
pathogenesis
action
MSCs,
NSCs,
HSCs
are
comprehensively
described.
Moreover,
treatment,
optimal
protocol
cell
administration,
recent
based
or
combined
also
discussed.
Biology,
Год журнала:
2022,
Номер
11(6), С. 939 - 939
Опубликована: Июнь 20, 2022
Spinal
cord
injury
(SCI)
initiates
detrimental
cellular
and
molecular
events
that
lead
to
acute
delayed
neuroinflammation.
Understanding
the
role
of
inflammatory
response
in
SCI
requires
insight
into
temporal
synthesis
mediators.
We
subjected
C57BL/6J
mice
investigated
reactions.
examined
activation,
recruitment,
polarization
microglia
infiltrating
immune
cells,
focusing
specifically
on
tumor
necrosis
factor
(TNF)
its
receptors
TNFR1
TNFR2.
In
phase,
TNF
expression
increased
glial
cells
neuron-like
followed
by
cells.
TNFR2
levels
phase
were
found
preferentially
neurons
respectively.
The
was
dominated
infiltration
granulocytes
macrophages.
Microglial/macrophage
Arg1
from
1-7
days
after
SCI,
an
increase
Itgam,
Cx3cr1,
P2ry12,
which
remained
elevated
throughout
study.
By
21
28
lesion
core
populated
galectin-3+,
CD68+,
CD11b+
microglia/macrophages,
surrounded
a
scar
consisting
GFAP+
astrocytes.
Findings
verified
postmortem
tissue
individuals
with
SCI.
Our
findings
support
consensus
future
neuroprotective
immunotherapies
should
aim
selectively
neutralize
signaling
while
sustaining
pro-regenerative
processes.
Frontiers in Bioengineering and Biotechnology,
Год журнала:
2023,
Номер
11
Опубликована: Апрель 28, 2023
Effectively
reducing
the
inflammatory
response
after
spinal
cord
injury
(SCI)
is
a
challenging
clinical
problem
and
subject
of
active
investigation.
This
study
employed
porous
scaffold-based
three
dimensional
long-term
culture
technique
to
obtain
human
umbilical
mesenchymal
stem
cell
(hUC-MSC)-derived
Small
Extracellular
Vesicles
(sEVs)
(three
over
time,
"4D-sEVs").
Moreover,
vesicle
size,
number,
inner
protein
concentrations
MSC
4D-sEVs
contained
altered
profiles
compared
with
those
derived
from
2D
conditions.
A
proteomics
analysis
suggested
broad
changes,
especially
significant
upregulation
Epidermal
Growth
Factors
Receptor
(EGFR)
Insulin-like
Factor
Binding
Protein
2
(IGFBP2)
in
2D-sEVs.
The
endocytosis
allowed
for
binding
EGFR
IGFBP2,
leading
downstream
STAT3
phosphorylation
IL-10
secretion
effective
induction
macrophages/microglia
polarization
pro-inflammatory
M1
anti-inflammatory
M2
phenotype,
both
vitro
injured
areas
rats
compressive/contusive
SCI.
reduction
neuroinflammation
delivery
site
epicenter
led
neuroprotection,
as
evidenced
by
number
surviving
neurons.
Therefore,
applying
this
novel
4D
culture-derived
could
effectively
curb
increase
tissue
repair
Biomedicine & Pharmacotherapy,
Год журнала:
2022,
Номер
157, С. 114011 - 114011
Опубликована: Ноя. 18, 2022
Spinal
cord
injury
(SCI)
is
a
serious
complication
of
the
central
nervous
system
(CNS)
after
spine
injury,
often
resulting
in
severe
sensory,
motor,
and
autonomic
dysfunction
below
level
injury.
To
date,
there
no
effective
treatment
strategy
for
SCI.
Recently,
stem
cell
therapy
has
brought
hope
to
patients
with
neurological
diseases.
Mesenchymal
cells
(MSCs)
are
considered
be
most
promising
source
cellular
SCI
due
their
immunomodulatory,
neuroprotective
angiogenic
potential.
Considering
limited
therapeutic
effect
MSCs
complex
pathophysiological
environment
following
SCI,
this
paper
not
only
reviews
specific
mechanism
facilitate
repair,
but
also
further
discusses
research
status
these
pluripotent
combined
other
approaches
promote
anatomical
functional
recovery
post-SCI.