Journal of Extracellular Vesicles,
Journal Year:
2022,
Volume and Issue:
11(5)
Published: May 1, 2022
Abstract
Research
on
tumour
cell‐derived
small
extracellular
vesicles
(sEVs)
that
regulate
microenvironment
(TME)
has
provided
strategies
for
targeted
therapy
of
head
and
neck
squamous
cell
carcinoma
(HNSCC).
Herein,
we
demonstrated
sEVs
derived
from
HNSCC
cancer
cells
carried
CD73
(sEVs
),
which
promoted
malignant
progression
mediated
immune
evasion.
The
phagocytosed
by
tumour‐associated
macrophages
(TAMs)
in
the
TME
induced
immunosuppression.
Higher
high
TAMs
infiltration
levels
were
correlated
with
poorer
prognosis,
while
activated
NF‐κB
pathway
TAMs,
thereby
inhibiting
function
increasing
cytokines
secretion
such
as
IL‐6,
IL‐10,
TNF‐α,
TGF‐β1.
absence
enhanced
sensitivity
anti‐PD‐1
through
reversed
Moreover,
circulating
increased
risk
lymph
node
metastasis
worse
prognosis.
Taken
together,
our
study
suggests
contributes
to
immunosuppression
is
a
potential
predictor
responses
checkpoint
HNSCC.
Exploration,
Journal Year:
2022,
Volume and Issue:
2(6)
Published: May 23, 2022
Immunotherapy
is
used
to
regulate
systemic
hyperactivation
or
hypoactivation
treat
various
diseases.
Biomaterial-based
immunotherapy
systems
can
improve
therapeutic
effects
through
targeted
drug
delivery,
immunoengineering,
etc.
However,
the
immunomodulatory
of
biomaterials
themselves
cannot
be
neglected.
In
this
review,
we
outline
with
functions
discovered
in
recent
years
and
their
applications
disease
treatment.
These
inflammation,
tumors,
autoimmune
diseases
by
regulating
immune
cell
function,
exerting
enzyme-like
activity,
neutralizing
cytokines,
The
prospects
challenges
biomaterial-based
modulation
are
also
discussed.
Frontiers in Cell and Developmental Biology,
Journal Year:
2020,
Volume and Issue:
8
Published: Dec. 9, 2020
Angiogenesis
and
osteogenesis
are
tightly
coupled
during
bone
modeling
remodeling
processes.
Here
we
reported
that
marrow
mesenchymal
stem
cell
(BMSC)-derived
exosomal
miR-29a
promotes
angiogenesis
in
vitro
vivo
.
BMSC-derived
exosomes
(BMSCs-Exos)
can
be
taken
up
by
human
umbilical
vein
endothelial
cells
(HUVECs)
promote
the
proliferation,
migration,
tube
formation
of
HUVECs.
MiRNA-29a
level
was
high
BMSCs-Exos
transported
into
HUVECs
to
regulate
angiogenesis.
VASH1
identified
as
a
direct
target
miR-29a,
mediating
effects
on
More
interestingly,
miR29a-loaded
from
engineered
BMSCs
(miR-29a-loaded
BMSCs-Exos)
showed
robust
ability
promoting
Taken
together,
these
findings
suggest
regulates
osteogenesis,
miR-29a-loaded
may
serve
potential
therapeutic
for
osteoporosis.
International Reviews of Immunology,
Journal Year:
2021,
Volume and Issue:
41(1), P. 4 - 18
Published: July 25, 2021
Metabolite
lactic
acid
has
always
been
regarded
as
a
metabolic
by-product
rather
than
bioactive
molecule.
Recently,
this
view
changed
since
it
was
discovered
that
can
be
used
signal
molecule
and
novel
transduction
functions
both
intracellular
extracellular,
which
regulate
key
in
the
immune
system.
In
recent
years,
more
evidence
shown
is
closely
related
to
metabolism
polarization
of
macrophages.
During
inflammation,
regulator
macrophage
metabolism,
prevent
excessive
inflammatory
responses;
malignant
tumors,
produced
by
tumor
tissues
promotes
tumor-associated
macrophages,
turn
progression.
review,
we
examined
relationship
between
metabolism.
We
further
discussed
how
plays
role
maintaining
homeostasis
well
biology
M1/M2
imbalance
human
diseases.
Potential
methods
target
treatment
inflammation
cancer
will
also
so
provide
new
strategies
for
Bioactive Materials,
Journal Year:
2022,
Volume and Issue:
22, P. 141 - 167
Published: Sept. 29, 2022
Currently,
there
are
no
clinical
drugs
available
to
treat
acute
kidney
injury
(AKI).
Given
the
high
prevalence
and
mortality
rate
of
AKI,
development
effectively
AKI
is
a
huge
unmet
medical
need
research
hotspot.
Although
existing
evidence
fully
demonstrates
that
reactive
oxygen
nitrogen
species
(RONS)
burst
at
site
major
contributor
progression,
heterogeneity,
complexity,
unique
physiological
structure
make
most
antioxidant
anti-inflammatory
small
molecule
ineffective
because
lack
targeting
side
effects.
Recently,
nanodrugs
with
intrinsic
through
control
size,
shape,
surface
properties
have
opened
exciting
prospects
for
treatment
AKI.
Many
emerged
address
limitations
current
treatments.
In
this
review,
we
systematically
summarized
first
time
about
emerging
exploit
pathological
features
overcome
traditional
small-molecule
achieve
efficacy.
First,
analyzed
structural
characteristics
main
mechanism
AKI:
hypoxia,
harmful
substance
accumulation-induced
RONS
renal
despite
multifactorial
initiation
heterogeneity
Subsequently,
introduced
strategies
used
improve
reviewed
advances
nano-RONS-sacrificial
agents,
nanozymes,
nanocarriers
antioxidants
drugs.
These
demonstrated
excellent
therapeutic
effects,
such
as
greatly
reducing
oxidative
stress
damage,
restoring
function,
low
Finally,
discussed
challenges
future
directions
translating
into
treatment.
Stem Cells International,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 18
Published: May 14, 2022
Mesenchymal
stem
cells
(MSCs)
have
been
widely
applied
to
regenerative
medicine
owing
their
multiple
differentiation,
self-renewal,
and
immunomodulatory
abilities.
Exosomes
are
cell-secreted
natural
nanovesicles
thought
be
mediators
of
intercellular
communication
material
transport.
The
therapeutic
potential
MSCs
can
largely
attributed
MSC-derived
exosomes
(MSC-exosomes).
Emerging
evidence
suggests
that
the
efficacy
MSC-exosomes
is
highly
dependent
on
status
MSCs,
optimization
extracellular
environment
affects
exosomal
content.
Pretreatment
methods
including
three-dimensional
cultures,
hypoxia,
other
biochemical
cues
shown
potentially
enhance
biological
activity
while
maintaining
or
enhancing
production.
On
hand,
engineering
means
desired
function
has
rapidly
gaining
attention.
In
particular,
biologically
active
molecule
encapsulation
membrane
modification
alter
functions
targeting
MSC-exosomes.
this
review,
we
summarize
two
possible
strategies
improve
MSC-exosomes:
preconditioning
approaches
exosomes.
We
also
explore
underlying
mechanisms
different
discuss
advantages
limitations
upcoming
clinical
applications.
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(17)
Published: April 20, 2023
Extracellular
vesicles
(EVs)
are
transport
secreted
by
living
cells
and
released
into
the
extracellular
environment.
Recent
studies
have
shown
that
EVs
serve
as
"messengers"
in
intercellular
inter-organismal
communication,
both
normal
pathological
processes.
EVs,
natural
nanocarriers,
can
deliver
bioactivators
therapy
with
their
endogenous
properties.
This
review
article
describes
engineering
of
sources,
isolation
method,
cargo
loading,
boosting
approach,
adjustable
targeting
EVs.
Furthermore,
summarizes
recent
progress
made
EV-based
delivery
systems
applications,
including
cancer,
cardiovascular
diseases,
liver,
kidney,
nervous
system
COVID-19
emphasizes
obstacles
challenges
therapies
possible
strategies.
Cellular and Molecular Immunology,
Journal Year:
2023,
Volume and Issue:
20(6), P. 626 - 650
Published: April 25, 2023
Abstract
Osteoarthritis
(OA)
is
a
degenerative
multifactorial
disease
with
concomitant
structural,
inflammatory,
and
metabolic
changes
that
fluctuate
in
temporal
patient-specific
manner.
This
complexity
has
contributed
to
refractory
responses
various
treatments.
MSCs
have
shown
promise
as
multimodal
therapeutics
mitigating
OA
symptoms
progression.
Here,
we
evaluated
15
randomized
controlled
clinical
trials
(RCTs)
11
nonrandomized
RCTs
using
culture-expanded
the
treatment
of
knee
OA,
found
net
positive
effects
on
pain
(improving
function
12/15
relative
baseline
11/15
control
groups
at
study
endpoints)
cartilage
protection
and/or
repair
(18/21
studies).
We
examined
MSC
dose,
tissue
origin,
autologous
vs.
allogeneic
origins
well
patient
phenotype,
endotype,
age,
sex
level
severity
key
parameters
parsing
effectiveness.
The
relatively
small
sample
size
610
patients
limited
drawing
definitive
conclusions.
Nonetheless,
noted
trends
toward
moderate
higher
doses
select
phenotypes
leading
structural
improvements
or
preservation.
Evidence
from
preclinical
studies
supportive
anti-inflammatory
immunomodulatory
effects,
but
additional
investigations
immunomodulatory,
chondroprotective
other
mechanisms
action
are
needed.
hypothesize
basal
“fitness”
correlates
efficacy,
this
hypothesis
needs
be
validated
future
studies.
conclude
roadmap
articulating
need
match
an
subset
defined
by
molecular
endotype
phenotype
basally
“fit”
engineered-to-be-fit-for-OA
well-designed,
data-intensive
advance
field.