ACS Omega,
Год журнала:
2024,
Номер
9(6), С. 6492 - 6504
Опубликована: Янв. 31, 2024
Extracellular
vesicles
(EVs)
are
increasingly
used
for
disease
diagnosis
and
treatment.
Among
them,
red
blood
cell-derived
EVs
(RBC-EVs)
have
attracted
great
attention
due
to
their
abundant
sources
low
risks
of
gene
transfer
(RBC-EVs
lack
nuclear
mitochondrial
DNA).
Here,
we
first
revealed
the
high
expression
level
membrane
protein
solute
carrier
family
4
member
1
(SLC4A1)
in
RBC-EVs
through
proteomic
analysis.
We
then
identified
several
binding
peptides
with
affinity
SLC4A1
extracellular
domain
(SLC4A1-EC)
from
phage
display
library
screening.
A
SLC4A1-EC
three
(XRB2,
XRE4,
XRH7)
were
assessed
vitro
using
surface
plasmon
resonance
analysis
SDS–polyacrylamide
gel
electrophoresis
(SDS–PAGE).
The
sites
polypeptides
further
predicted
by
LigPlot
+
analysis,
results
showed
that
these
could
bind
part
hydrophobic
residues
SLC4A1-EC.
efficiency
anchor
was
verified
flow
cytometry
fluorescence
imaging.
In
conclusion,
successfully
screened
specific
RBC-EV-targeting
which
potentially
be
utilized
isolating
RBC-derived
serum
samples.
More
importantly,
this
peptide
coupled
targeting
modify
drug
delivery.
Our
work
will
provide
a
viable
method
optimizing
function
RBC-EVs.
International Journal of Nanomedicine,
Год журнала:
2024,
Номер
Volume 19, С. 1363 - 1383
Опубликована: Фев. 1, 2024
Osteoporosis
(OP)
affects
millions
of
people
worldwide,
especially
postmenopausal
women
and
the
elderly.
Although
current
available
anti-OP
agents
can
show
promise
in
slowing
down
bone
resorption,
most
are
not
specifically
delivered
to
hard
tissue,
causing
significant
toxicity.
A
bone-targeted
nanodrug
delivery
system
reduce
side
effects
precisely
deliver
drug
candidates
bone.
This
review
focuses
on
progress
nanoparticles
OP
therapy.
We
enumerate
existing
medications,
types
categorize
pairs
common
bone-targeting
functional
groups.
Finally,
we
summarize
potential
use
treatment.
Ongoing
research
into
development
targeted
ligands
nanocarriers
will
continue
expand
possibilities
OP-targeted
therapies
clinical
application.
European journal of medical research,
Год журнала:
2024,
Номер
29(1)
Опубликована: Янв. 3, 2024
Abstract
Early
diagnosis
and
pharmacological
treatment
of
central
nervous
system
(CNS)
diseases
has
been
a
long-standing
challenge
for
clinical
research
due
to
the
presence
blood–brain
barrier.
Specific
proteins
RNAs
in
brain-derived
extracellular
vesicles
(EVs)
usually
reflect
corresponding
state
brain
disease,
therefore,
EVs
can
be
used
as
diagnostic
biomarkers
CNS
diseases.
In
addition,
engineered
fused
target
cells
delivery
cargo,
demonstrating
great
potential
nanocarrier
platform.
We
review
progress
markers
drug
carriers
neurological
The
main
areas
include
visual
imaging,
biomarker
loading
therapy
different
types
It
is
hoped
that
increased
knowledge
will
facilitate
their
translation
Theranostics,
Год журнала:
2024,
Номер
14(8), С. 3246 - 3266
Опубликована: Янв. 1, 2024
The
rapid
advancement
of
mRNA
as
vaccines
and
therapeutic
agents
in
the
biomedical
field
has
sparked
hope
fight
against
untreatable
diseases.Successful
clinical
application
therapeutics
largely
depends
on
carriers.Recently,
a
new
exciting
focus
emerged
natural
cell-derived
vesicles.These
nanovesicles
offer
many
functions,
including
enhanced
drug
delivery
capabilities
immune
evasion,
thereby
presenting
unique
promising
platform
for
effective
safe
therapeutics.In
this
study,
we
summarize
characteristics
properties
biomimetic
systems
particular,
discuss
features
cellular
membrane-derived
vesicles
(CDVs)
combination
synthetic
with
CDVs.
Cells,
Год журнала:
2024,
Номер
13(7), С. 606 - 606
Опубликована: Март 30, 2024
In
vitro
and
preclinical
in
vivo
research
the
last
35
years
has
clearly
highlighted
crucial
physiopathological
role
of
glial
cells,
namely
astrocytes/microglia/oligodendrocytes
satellite
cells/Schwann
cells
central
peripheral
nervous
system,
respectively.
Several
possible
pharmacological
targets
to
various
neurodegenerative
disorders
painful
conditions
have
therefore
been
successfully
identified,
including
receptors
enzymes,
mediators
neuroinflammation.
However,
translation
these
promising
data
a
clinical
setting
is
often
hampered
by
both
technical
biological
difficulties,
making
it
necessary
perform
experiments
on
human
models
diseases.
this
review
we
will,
therefore,
summarize
most
relevant
contribution
pathologies
their
modulation
based
obtained
post-mortem
tissues
iPSC-derived
brain
organoids.
The
possibility
an
visualization
glia
reaction
neuroinflammation
patients
will
be
also
discussed.
Abstract
Central
Nervous
System
(CNS)
disorders
represent
a
profound
public
health
challenge
that
affects
millions
of
people
around
the
world.
Diseases
such
as
Alzheimer’s
disease
(AD),
Parkinson’s
(PD),
and
traumatic
brain
injury
(TBI)
exemplify
complexities
diversities
complicate
their
early
detection
development
effective
treatments.
Amid
these
challenges,
emergence
nanotechnology
extracellular
vesicles
(EVs)
signals
new
dawn
for
treating
diagnosing
CNS
ailments.
EVs
are
cellularly
derived
lipid
bilayer
nanosized
particles
pivotal
in
intercellular
communication
within
have
potential
to
revolutionize
targeted
therapeutic
delivery
identification
novel
biomarkers.
Integrating
with
amplifies
diagnostic
capabilities,
opening
avenues
managing
diseases.
This
review
focuses
on
examining
fascinating
interplay
between
theranostics.
Through
highlighting
remarkable
advancements
unique
methodologies,
we
aim
offer
valuable
perspectives
how
approaches
can
bring
about
revolutionary
change
management.
The
objective
is
harness
distinctive
attributes
forge
personalized,
efficient
interventions
disorders,
thereby
providing
beacon
hope
affected
individuals.
In
short,
confluence
heralds
promising
frontier
impactful
treatments
against
diseases,
which
continue
pose
significant
challenges.
By
focusing
personalized
powerful
methods,
might
improve
quality
patients.
International Journal of Nanomedicine,
Год журнала:
2024,
Номер
Volume 19, С. 4279 - 4295
Опубликована: Май 1, 2024
Ischemic
stroke,
being
a
prominent
contributor
to
global
disability
and
mortality,
lacks
an
efficacious
therapeutic
approach
in
current
clinical
settings.
Neural
stem
cells
(NSCs)
are
type
of
cell
that
only
found
inside
the
nervous
system.
These
can
differentiate
into
various
kinds
cells,
potentially
regenerating
or
restoring
neural
networks
within
areas
brain
have
been
destroyed.
This
review
begins
by
providing
introduction
existing
approaches
for
ischemic
followed
examination
promise
limits
associated
with
utilization
NSCs
treatment
stroke.
Subsequently,
comprehensive
overview
was
conducted
synthesize
literature
on
underlying
processes
cell-derived
small
extracellular
vesicles
(NSC-sEVs)
transplantation
therapy
context
mechanisms
encompass
neuroprotection,
inflammatory
response
suppression,
endogenous
nerve
vascular
regeneration
facilitation.
Nevertheless,
translation
NSC-sEVs
is
hindered
challenges
such
as
inadequate
targeting
efficacy
insufficient
content
loading.
In
light
these
limitations,
we
compiled
advancements
utilizing
modified
treating
stroke
based
methods
vesicle
modification.
conclusion,
examining
NSC-sEVs-based
anticipated
be
both
fundamental
applied
investigations
about
The
effects
of
chronically
stressing
male
mice
can
be
transmitted
across
generations
by
stress-specific
changes
in
their
sperm
miRNA
content,
which
induce
phenotypes
offspring.
However,
how
each
stress
paradigm
alters
the
levels
distinct
sets
miRNAs
is
not
known.
We
showed
previously
that
exposure
to
chronic
social
instability
(CSI)
results
elevated
anxiety
and
reduced
sociability
specifically
female
offspring
multiple
because
it
reduces
miR-34c
stressed
males
unstressed
Here,
we
describe
evidence
astrocyte-derived
exosomes
(A-Exos)
carrying
mediate
CSI
has
this
transgenerational
effect
on
sperm.
found
decreases
carried
A-Exos
prefrontal
cortex
amygdala,
as
well
blood
males.
Importantly,
are
also
these
tissues
F1
offspring,
who
despite
being
exposed
stress,
exhibit
transmit
same
stress-associated
traits
Furthermore,
restoring
content
CSI-stressed
intravenous
injection
miR-34c-containing
restores
These
findings
reveal
an
unexpected
role
for
maintaining
a
process
when
suppressed
mediates
example
epigenetic
inheritance.
Molecular Neurobiology,
Год журнала:
2025,
Номер
unknown
Опубликована: Март 17, 2025
Abstract
Neurodegenerative
diseases
(NDs)
like
Alzheimer’s,
Parkinson’s,
and
ALS
rank
among
the
most
challenging
global
health
issues,
marked
by
substantial
obstacles
in
early
diagnosis
effective
treatment.
Current
diagnostic
techniques
frequently
demonstrate
inadequate
sensitivity
specificity,
whilst
conventional
treatment
strategies
encounter
challenges
related
to
restricted
bioavailability
insufficient
blood–brain
barrier
(BBB)
permeability.
Recently,
exosomes—nanoscale
vesicles
packed
with
proteins,
RNAs,
lipids—have
emerged
as
promising
agents
potential
reshape
therapeutic
approaches
these
diseases.
Unlike
drug
carriers,
they
naturally
traverse
BBB
can
deliver
bioactive
molecules
affected
neural
cells.
Their
molecular
cargo
influence
cell
signaling,
reduce
neuroinflammation,
potentially
slow
neurodegenerative
progression.
Moreover,
exosomes
serve
non-invasive
biomarkers,
enabling
precise
while
allowing
real-time
disease
monitoring.
Additionally,
engineered
exosomes,
loaded
molecules,
enhance
this
capability
targeting
diseased
neurons
overcoming
barriers.
By
offering
enhanced
reduced
immunogenicity,
an
ability
bypass
physiological
limitations,
exosome-based
present
a
transformative
advantage
over
existing
approaches.
This
review
examines
multifaceted
role
of
NDDs,
emphasizing
their
capabilities,
intrinsic
functions,
advanced
vehicles.