Vaccines,
Journal Year:
2024,
Volume and Issue:
12(11), P. 1282 - 1282
Published: Nov. 15, 2024
Milk-derived
extracellular
vesicles
(mEVs)
are
emerging
as
promising
therapeutic
candidates
due
to
their
unique
properties
and
versatile
functions.
These
play
a
crucial
role
in
immunomodulation
by
influencing
macrophage
differentiation
cytokine
production,
potentially
aiding
the
treatment
of
conditions
such
bone
loss,
fibrosis,
cancer.
mEVs
also
have
capacity
modulate
gut
microbiota
composition,
which
may
alleviate
symptoms
inflammatory
bowel
diseases
promote
intestinal
barrier
integrity.
Their
potential
drug
delivery
vehicles
is
significant,
enhancing
stability,
solubility,
bioavailability
anticancer
agents
while
supporting
wound
healing
reducing
inflammation.
Additionally,
bovine
exhibit
anti-aging
protect
skin
cells
from
UV
damage.
As
vaccine
platforms,
offer
advantages
including
biocompatibility,
antigen
protection,
ability
elicit
robust
immune
responses
through
targeted
specific
cells.
Despite
these
applications,
challenges
persist,
complex
roles
cancer,
effective
loading,
regulatory
hurdles,
need
for
standardized
production
methods.
Achieving
high
targeting
specificity
understanding
long-term
effects
mEV-based
therapies
essential
clinical
translation.
Ongoing
research
aims
optimize
mEV
methods,
enhance
capabilities,
conduct
rigorous
preclinical
studies.
By
addressing
challenges,
hold
revolutionize
development
delivery,
ultimately
improving
outcomes
across
various
medical
fields.
Journal of Extracellular Biology,
Journal Year:
2024,
Volume and Issue:
3(6)
Published: June 1, 2024
Abstract
Extracellular
vesicles
(EVs)
are
nanosized
with
a
lipid
bilayer
that
secreted
by
cells
and
play
critical
role
in
cell‐to‐cell
communication.
Despite
the
promising
reports
regarding
their
diagnostic
therapeutic
potential,
utilization
of
EVs
clinical
setting
is
limited
due
to
insufficient
information
about
cargo
lack
standardization
isolation
analysis
methods.
Considering
protein
cargos
as
key
contributors
potency,
we
conducted
tandem
mass
tag
(TMT)
quantitative
proteomics
three
subpopulations
mesenchymal
stem
cell
(MSC)‐derived
obtained
through
different
techniques:
ultracentrifugation
(UC),
high‐speed
centrifugation
(HS),
on
sucrose
cushion
(SU).
Subsequently,
checked
EV
marker
expression,
size
distribution,
morphological
characterization,
followed
bioinformatic
analysis.
The
proteome
results
revealed
these
exhibit
distinct
molecular
functional
characteristics.
choice
method
impacts
isolated
isolating
EVs.
Specifically,
(HS)
exhibited
higher
abundance
ribosomal
mitochondrial
proteins.
Functional
apoptosis
assays
comparing
mitochondria
methods
HS‐EVs,
but
not
other
EVs,
induced
early
cancer
cells.
On
hand,
using
(SU)
(UC)
demonstrated
proteins
primarily
involved
immune
response,
cell‐cell
interactions
extracellular
matrix
interactions.
Our
analyses
unveil
notable
disparities
associated
biological
functions
among
subpopulations,
underscoring
importance
meticulously
selecting
resultant
based
intended
application.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 3, 2025
ABSTRACT
This
study
presents
a
novel
method
and
device
for
the
hydrodynamic
production
of
extracellular
vesicles
(EVs)
derived
from
biomimetic
multicellular
3D
spheroids,
enabling
high-throughput
particle
release
that
is
10
to
20
times
higher
than
in
non-stimulated
conditions.
The
facilitates
formation
spheroids
human
mesenchymal
stem
cells
(hMSCs),
offering
an
all-in-one
approach
both
spheroid
generation
EV
release.
Production
are
reduced
just
few
hours,
with
yield
further
increased
by
alternating
periods
high
flow
recovery
sequential
approach.
Using
this
system,
we
explored
impact
starvation
conditions
on
protein
cargo
EVs,
identifying
distinct
markers
through
proteomics.
Specifically,
stimulation
enriched
EVs
plasma
membrane-derived
mitochondrial
proteins,
revealing
divergent
biogenesis
pathways.
Importantly,
produced
exhibited
therapeutic
properties,
demonstrated
effects
wound
healing,
angiogenesis,
anti-inflammatory
responses,
some
showing
enhanced
efficacy
under
stimulation.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: Jan. 27, 2025
Diabetic
wounds
are
characterized
by
chronic
inflammation,
reduced
angiogenesis,
and
insufficient
collagen
deposition,
leading
to
impaired
healing.
Extracellular
vesicles
(EVs)
derived
from
adipose-derived
mesenchymal
stem
cells
(ADSC)
offer
a
promising
cell-free
therapeutic
strategy,
yet
their
efficacy
immunomodulation
can
be
enhanced
through
bioactivation.
In
this
study,
we
developed
calcium
silicate
(CS)-stimulated
ADSC-derived
EVs
(CSEV)
incorporated
into
hydrogels
create
sustained-release
system
for
promoting
diabetic
wound
CSEV
exhibited
protein
content,
surface
marker
expression,
bioactive
cargo
enriched
with
pro-angiogenic
anti-inflammatory
factors.
vitro,
CSEV-loaded
significantly
reactive
oxygen
species
production,
promoted
cell
proliferation
migration
compared
standard
EV-loaded
collagen.
Cytokine
profiling
revealed
the
upregulation
of
cytokines
extracellular
matrix
components,
highlighting
immunomodulatory
regenerative
potential.
vivo,
histological
evaluation
rabbit
models
treated
superior
reepithelialization
organized
indicating
accelerated
closure.
These
findings
underscore
potential
as
an
innovative
effective
platform
enhancing
healing
simultaneously
addressing
inflammation
tissue
regeneration.
Stem Cell Research & Therapy,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 21, 2025
Mesenchymal
stem
cells
(MSCs),
an
accessible
and
less
ethically
controversial
class
of
adult
cells,
have
demonstrated
significant
efficacy
in
treating
a
wide
range
diseases
both
the
preclinical
clinical
phases.
However,
we
do
not
yet
clear
understanding
mechanisms
by
which
MSCs
exert
their
therapeutic
effects
vivo.
We
found
that
transplanted
go
apoptotic
fate
within
24
h
vivo
irrespective
route
administration.
Still,
short-term
survival
affect
long-term
efficacy.
An
increasing
number
studies
transplantation
(ApoMSCs)
show
similar
or
even
better
than
viable
MSCs,
including
variety
disease
models
such
as
inflammatory
diseases,
skin
damage,
bone
organ
etc.
Although
exact
mechanism
has
to
be
explored,
recent
shown
undergo
apoptosis
are
phagocytosed
phagocytes,
thereby
exerting
immunomodulatory
effects.
The
extracellular
vesicles
secreted
ApoMSCs
(MSC-ApoEVs)
play
role
promoting
immunomodulation,
endogenous
cell
regeneration,
angiogenesis
due
properties
inheritance
molecular
characteristics
from
parental
MSCs.
On
this
basis,
review
aims
deeply
explore
applications
secretion
MSC-ApoEVs,
well
challenges
they
face.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 13, 2024
Chronic
kidney
disease
(CKD)
is
a
progressive
disorder
characterized
by
structural
and
functional
changes
in
the
kidneys,
providing
global
health
challenge
with
significant
impacts
on
mortality
rates.
Extracellular
vesicles
(EVs),
are
vital
physiological
pathological
processes
associated
CKD.
They
have
been
shown
to
modulate
key
pathways
involved
renal
injury,
including
inflammation,
fibrosis,
apoptosis,
oxidative
stress.
Currently,
application
research
of
EVs
diagnosis
treatment
CKD
highly
prevalent.
However,
there
currently
lack
standardized
guidelines
for
their
application,
various
methodologies
advantages
limitations.
Consequently,
we
present
an
comprehensive
summary
elucidating
multifaceted
involvement
both
aspects
Furthermore,
explore
potential
as
biomarkers
diverse
therapeutic
roles
This
review
provides
overview
current
state
management
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 7, 2024
Abstract
Extracellular
vesicles
(EVs)
are
nanosized
with
a
lipid
bilayer
that
secreted
by
cells
and
play
critical
role
in
cell-to-cell
communication.
Despite
the
promising
reports
regarding
their
diagnostic
therapeutic
potential,
utilization
of
EVs
clinical
setting
is
limited
due
to
insufficient
information
about
cargo
lack
standardization
isolation
analysis
methods.
Considering
protein
cargos
as
key
contributors
potency,
we
conducted
tandem
mass
tag
(TMT)
quantitative
proteomics
three
subpopulations
mesenchymal
stem
cell
(MSC)-derived
obtained
through
different
techniques:
ultracentrifugation
(UC),
high-speed
centrifugation
(HS),
on
sucrose
cushion
(SU).
Subsequently,
checked
EV
marker
expression,
size
distribution,
morphological
characterization,
followed
bioinformatic
analysis.
The
proteome
results
revealed
these
exhibit
distinct
molecular
functional
characteristics.
choice
method
impacts
isolated
isolating
EVs.
Specifically,
(HS)
exhibited
higher
abundance
ribosomal
mitochondrial
proteins.
Functional
apoptosis
assays
comparing
mitochondria
methods
HS-EVs,
but
not
other
EVs,
induced
early
cancer
cells.
On
hand,
using
(SU)
(UC)
demonstrated
proteins
primarily
involved
immune
response,
cellLJcell
interactions,
extracellular
matrix
interactions.
Our
analyses
unveil
notable
disparities
associated
biological
functions
among
subpopulations,
underscoring
importance
meticulously
selecting
resultant
based
intended
application.
Biology,
Journal Year:
2024,
Volume and Issue:
13(9), P. 716 - 716
Published: Sept. 12, 2024
In
recent
years,
knowledge
of
cell-released
extracellular
vesicle
(EV)
functions
has
undergone
rapid
growth.
EVs
are
membrane
vesicles
loaded
with
proteins,
nucleic
acids,
lipids,
and
bioactive
molecules.
Once
released
into
the
space,
delivered
to
target
cells
that
may
go
through
modifications
in
physiological
or
pathological
conditions.
nano
shuttles
a
crucial
role
promoting
short-
long-distance
cell-cell
communication.
Comprehension
mechanism
regulates
this
process
is
benefit
for
both
medicine
basic
science.
Currently,
attract
immense
interest
precision
nanomedicine
their
potential
use
diagnosis,
prognosis,
therapies.
This
review
reports
latest
advances
EV
studies,
focusing
on
nature
features
conventional
emerging
methodologies
used
separation,
characterization,
visualization.
By
searching
an
extended
portion
relevant
literature,
work
aims
give
summary
nanomedical
applications
EVs.
Moreover,
concerns
require
further
studies
before
translation
clinical
discussed.