Heliyon,
Год журнала:
2024,
Номер
10(3), С. e25400 - e25400
Опубликована: Фев. 1, 2024
Articular
cartilage
injury
is
a
prevalent
clinical
condition
resulting
from
trauma,
tumors,
infection,
osteoarthritis,
and
other
factors.
The
intrinsic
lack
of
blood
vessels,
nerves,
lymphatic
vessels
within
tissue
severely
limits
its
self-regenerative
capacity
after
injury.
Current
treatment
options,
such
as
conservative
drug
therapy
joint
replacement,
have
inherent
limitations.
Achieving
perfect
regeneration
repair
articular
remains
an
ongoing
challenge
in
the
field
regenerative
medicine.
Tissue
engineering
has
emerged
key
focus
research,
aiming
to
utilize
cultured
expanded
cells
combined
with
suitable
scaffold
materials
create
viable,
functional
tissues.
This
review
article
encompasses
latest
advancements
seed
cells,
scaffolds,
cytokines.
Additionally,
role
stimulatory
factors
including
cytokines
growth
factors,
genetic
techniques,
biophysical
stimulation,
bioreactor
systems,
well
scaffolding
natural
synthetic
nanostructured
scaffolds
tissues
are
discussed.
Finally,
we
also
outline
signaling
pathways
involved
regeneration.
Our
provides
valuable
insights
for
scholars
address
complex
problem
repair.
International Journal of Molecular Sciences,
Год журнала:
2021,
Номер
22(5), С. 2619 - 2619
Опубликована: Март 5, 2021
Osteoarthritis
(OA)
is
a
degenerative
and
chronic
joint
disease
characterized
by
clinical
symptoms
distortion
of
tissues.
It
primarily
damages
cartilage,
causing
pain,
swelling,
stiffness
around
the
joint.
major
cause
disability
pain.
The
prevalence
OA
expected
to
increase
gradually
with
aging
population
increasing
obesity.
Many
potential
therapeutic
advances
have
been
made
in
recent
years
due
improved
understanding
underlying
mechanisms,
diagnosis,
management
OA.
Embryonic
stem
cells
induced
pluripotent
differentiate
into
chondrocytes
or
mesenchymal
(MSCs)
can
be
used
as
source
injectable
treatments
cavity.
MSCs
are
known
most
studied
cell
therapy
products
cell-based
owing
their
ability
immunomodulatory
properties.
They
improve
cartilage
recovery
ultimately
restore
healthy
joints.
However,
despite
currently
available
therapies
research,
unfulfilled
medical
needs
persist
for
treatment.
In
this
review,
we
focused
on
contents
non-cellular
cellular
OA,
briefly
summarized
results
trials
lay
solid
application
basis
research.
Journal of Cosmetic Dermatology,
Год журнала:
2021,
Номер
20(12), С. 3759 - 3781
Опубликована: Ноя. 6, 2021
Androgenetic
alopecia
(AGA)
is
the
most
common
form
of
hair
loss
consisting
a
characteristic
receding
frontal
hairline
in
men
and
diffuse
thinning
women,
with
retention,
can
impact
an
individual's
quality
life.
The
condition
primarily
mediated
by
5-alpha-reductase
dihydrotestosterone
(DHT)
which
causes
follicles
to
undergo
miniaturization
shortening
successive
anagen
cycles.
Although
variety
medical,
surgical,
light-based
nutraceutical
treatment
options
are
available
slow
or
reverse
progression
AGA,
it
be
challenging
select
appropriate
therapies
for
this
chronic
condition.To
highlight
androgenetic
taking
into
consideration
efficacy,
side
effect
profiles,
practicality
(compliance),
costs
help
clinicians
offer
ethically
regimens
their
patients.A
literature
search
was
conducted
using
electronic
databases
(Medline,
PubMed,
Embase,
CINAHL,
EBSCO)
textbooks,
addition
authors'
other
practitioners'
clinical
experiences
treating
alopecia,
findings
presented
here.Although
topical
minoxidil,
oral
finasteride,
low-level
light
therapy
only
FDA-approved
treat
they
just
fraction
available,
including
modalities,
hormonal
therapies,
nutraceuticals,
PRP
exosome
treatments,
transplantation.Androgenetic
remains
as
selection
involves
ethical,
evidence-based
decision-making
each
individual
patient's
needs,
compliance,
budget,
extent
loss,
aesthetic
goals,
independent
potential
financial
benefits
practitioners.
Military Medical Research,
Год журнала:
2022,
Номер
9(1)
Опубликована: Ноя. 19, 2022
Abstract
Bone,
cartilage,
and
soft
tissue
regeneration
is
a
complex
spatiotemporal
process
recruiting
variety
of
cell
types,
whose
activity
interplay
must
be
precisely
mediated
for
effective
healing
post-injury.
Although
extensive
strides
have
been
made
in
the
understanding
immune
microenvironment
processes
governing
bone,
regeneration,
clinical
translation
these
mechanisms
remains
challenge.
Regulation
increasingly
becoming
favorable
target
regeneration;
therefore,
an
in-depth
communication
between
cells
functional
would
valuable.
Herein,
we
review
regulatory
role
promotion
maintenance
stem
states
context
repair
regeneration.
We
discuss
roles
various
subsets
introduce
novel
strategies,
example,
biomaterial-targeting
activity,
aimed
at
regulating
healing.
Understanding
crosstalk
pathways
may
shed
light
on
new
therapeutic
opportunities
enhancing
through
regulation
microenvironment.
International Journal of Molecular Sciences,
Год журнала:
2021,
Номер
22(8), С. 3851 - 3851
Опубликована: Апрель 8, 2021
Extracellular
vesicles
(EVs)
derived
from
mesenchymal
stem
cells
isolated
both
bone
marrow
(BMSCs)
and
adipose
tissue
(ADSCs)
show
potential
therapeutic
effects.
These
often
a
similar
beneficial
effect
on
regeneration,
but
in
some
contexts,
they
exert
different
biological
properties.
To
date,
comparison
of
their
molecular
cargo
that
could
explain
the
is
not
available.
Here,
we
demonstrated
ADSC-EVs,
BMSC-EVs,
promote
wound
healing
murine
model
diabetic
wounds.
Besides
general
similarity,
bioinformatic
analysis
protein
miRNA
highlighted
important
differences
between
these
two
types
EVs.
Molecules
present
exclusively
ADSC-EVs
were
highly
correlated
to
angiogenesis,
whereas
those
expressed
BMSC-EVs
preferentially
involved
cellular
proliferation.
Finally,
vitro
confirmed
ADSC
exploited
skin
such
as
fibroblasts,
keratinocytes
endothelial
cells,
through
processes.
Consistent
with
analyses,
shown
mainly
proliferation,
major
angiogenesis.
Taken
together,
results
provide
deeper
comparative
information
impact
regenerative
processes
essential
for
healing.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(7), С. 6405 - 6405
Опубликована: Март 29, 2023
Osteoarthritis
(OA)
is
a
chronic
disease
and
the
most
common
orthopedic
disorder.
A
vast
majority
of
social
OA
burden
related
to
hips
knees.
The
prevalence
knee
varied
across
studies
such
differences
are
reflected
by
heterogeneity
data
reported
conducted
worldwide.
complete
understanding
pathogenetic
mechanisms
underlying
this
pathology
essential.
inflammatory
process
starts
in
synovial
membrane
with
activation
immune
system,
involving
both
humoral
cellular
mediators.
crucial
role
played
so-called
“damage-associated
molecular
patterns”
(DAMPs).
Mesenchymal
stem
cells
(MSCs)
may
be
promising
option
among
all
possible
therapeutic
options.
However,
many
issues
still
debated,
as
best
cell
source,
their
nature,
right
amount.
Further
needed
clarify
remaining
doubts.
This
review
provides
an
overview
recent
relevant
on
mechanism
cartilage
damage
OA,
including
current
approaches
regenerative
medicine.
International Journal of Molecular Sciences,
Год журнала:
2021,
Номер
22(2), С. 684 - 684
Опубликована: Янв. 12, 2021
Tissue
engineering
has
been
an
inveterate
area
in
the
field
of
regenerative
medicine
for
several
decades.
However,
there
remains
limitations
to
engineer
and
regenerate
tissues.
Targeted
therapies
using
cell-encapsulated
hydrogels,
such
as
mesenchymal
stem
cells
(MSCs),
are
capable
reducing
inflammation
increasing
potential
In
addition,
use
MSC-derived
nano-scale
secretions
(i.e.,
exosomes)
promising.
Exosomes
originate
from
multivesicular
division
have
high
therapeutic
potential,
yet
neither
self-replicate
nor
cause
auto-immune
reactions
host.
To
maintain
their
biological
activity
allow
a
controlled
release,
these
paracrine
factors
can
be
encapsulated
biomaterials.
Among
different
types
biomaterials
which
exosome
infusion
is
exploited,
hydrogels
proven
most
user-friendly,
economical,
accessible
material.
this
paper,
we
highlight
importance
MSCs
exosomes
tissue
biomaterial
strategies
used
fabricating
exosome-based
biomaterials,
facilitate
hard
soft
engineering.
Cells,
Год журнала:
2020,
Номер
9(3), С. 680 - 680
Опубликована: Март 10, 2020
Atopic
dermatitis
(AD)
is
a
multifactorial,
heterogeneous
disease
associated
with
epidermal
barrier
disruption
and
intense
systemic
inflammation.
Previously,
we
showed
that
exosomes
derived
from
human
adipose
tissue-derived
mesenchymal
stem
cells
(ASC-exosomes)
attenuate
AD-like
symptoms
by
reducing
multiple
inflammatory
cytokine
levels.
Here,
investigated
ASC-exosomes’
effects
on
skin
restoration
analyzing
protein
lipid
contents.
We
found
subcutaneous
injection
of
ASC-exosomes
in
an
oxazolone-induced
model
remarkably
reduced
trans-epidermal
water
loss,
while
enhancing
stratum
corneum
(SC)
hydration
markedly
decreasing
the
levels
cytokines
such
as
IL-4,
IL-5,
IL-13,
TNF-α,
IFN-γ,
IL-17,
TSLP,
all
dose-dependent
manner.
Interestingly,
induced
production
ceramides
dihydroceramides.
Electron
microscopic
analysis
revealed
enhanced
lamellar
bodies
formation
layer
at
interface
SC
granulosum
treatment.
Deep
RNA
sequencing
lesions
demonstrated
restores
expression
genes
involved
barrier,
metabolism,
cell
cycle,
response
diseased
area.
Collectively,
our
results
suggest
effectively
restore
functions
AD
facilitating
de
novo
synthesis
ceramides,
resulting
promising
cell-free
therapeutic
option
for
treating
AD.
Glioblastoma
(GBM)
is
one
of
the
most
fatal
central
nervous
system
tumors
and
lacks
effective
or
sufficient
therapies.
Ferroptosis
a
newly
discovered
method
programmed
cell
death
opens
new
direction
for
GBM
treatment.
However,
poor
blood-brain
barrier
(BBB)
penetration,
reduced
tumor
targeting
ability,
potential
compensatory
mechanisms
hinder
effectiveness
ferroptosis
agents
during
Here,
novel
composite
therapeutic
platform
combining
magnetic
features
drug
delivery
properties
nanoparticles
with
BBB
penetration
abilities
siRNA
encapsulation
engineered
exosomes
therapy
presented.
This
can
be
enriched
in
brain
under
local
localization
angiopep-2
peptide-modified
trigger
transcytosis,
allowing
particles
to
cross
target
cells
by
recognizing
LRP-1
receptor.
Synergistic
achieved
combined
triple
actions
disintegration
dihydroorotate
dehydrogenase
glutathione
peroxidase
4
defense
axis
Fe