Exosomes as Biomarkers and Therapeutic Agents in Neurodegenerative Diseases: Current Insights and Future Directions
Sam Dehghani,
Ozgecan Ocakcı,
Pars Tan Hatipoglu
и другие.
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.
Язык: Английский
Chiral Carbon Nanodots Modulate α‐Synuclein Homeostasis to Combat Parkinson's Disease
Small Methods,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 15, 2025
Abstract
Inhibiting
α‐synuclein
(α‐syn)
aggregation
is
an
effective
treatment
for
Parkinson's
disease
(PD),
and
chiral
recognition
of
proteins
offers
a
novel
strategy
designing
efficient
inhibitors.
However,
the
impact
selectivity
on
α‐syn
its
regulatory
mechanisms
remain
ambiguous.
In
this
work,
it
synthesized
carbon
nanodots
(CNDs),
including
L‐CNDs,
D‐CNDs,
DL‐CNDs,
found
that
D‐CNDs
exhibited
most
potent
inhibitory
effect
aggregation.
¹H‐¹⁵N
heteronuclear
single
quantum
coherence
nuclear
magnetic
resonance
spectroscopy
revealed
CNDs
primarily
interact
with
through
electrostatic
interactions,
specifically
targeting
key
aggregation‐prone
residues,
thereby
disrupting
β‐sheet
formation
reducing
fibril
assembly.
contrast,
L‐CNDs
DL‐CNDs
limited
effects,
attributed
to
their
weak
affinity
non‐amyloid‐β
component
region.
Moreover,
efficiently
crossed
blood‐brain
barrier,
significantly
reduced
accumulation,
alleviated
neuronal
damage,
ameliorated
cognitive
function.
This
work
underlines
critical
role
chirality
in
modulating
provides
developing
enantiomer‐selective
inhibitors
PD
therapy.
Язык: Английский