Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(12), P. 2665 - 2665
Published: Nov. 22, 2024
Liver
fibrosis
represents
a
common
pathway
in
the
progression
of
various
chronic
liver
diseases
towards
cirrhosis
and
failure.
Extracellular
vesicles
(EVs)
are
membrane-enclosed
particles
secreted
by
diverse
cell
types,
including
exosomes,
microvesicles,
apoptotic
vesicles,
recently
identified
migrasomes.
These
can
be
taken
up
recipient
cells,
thereby
modulating
their
function
through
transport
cargo
molecules.
EVs
facilitate
intercellular
communication
play
significant
role
development
fibrosis.
Moreover,
detection
body
fluids
offers
sensitive
diagnostic
tools
for
assessing
Additionally,
may
serve
as
therapeutic
targets,
potential
agents,
drug
delivery
vehicles.
This
article
reviews
recent
advances
field
concerning
related
diseases,
with
particular
focus
on
newly
discovered
migrasomes
intracellular
crosstalk
within
liver.
Cancer Cell International,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: March 25, 2025
Migrasomes
are
a
newly
discovered
type
of
extracellular
vesicle
(EV)
formed
during
cell
migration,
playing
pivotal
role
in
intercellular
communication.
These
vesicles
generated
by
retracting
fibers
migrating
cells
and
encapsulate
various
molecules,
such
as
proteins,
lipids,
RNA,
allowing
the
transfer
biochemical
signals
to
neighboring
cells.
Current
evidence
suggests
that
migrasomes
involved
wide
range
physiological
processes
embryogenesis,
angiogenesis,
immune
modulation,
mitochondrial
quality
control.
Moreover,
implicated
pathological
conditions,
including
cancer
metastasis,
cardiovascular
diseases,
viral
infections.
To
fully
understand
their
significance,
it
is
critical
first
explore
molecular
mechanisms
underlying
formation
function.
Recent
studies
have
shed
light
on
biogenesis,
release,
biological
properties
migrasomes,
all
which
key
understanding
cell-to-cell
In
this
review,
we
provide
an
up-to-date
summary
migrasome
characterization,
activities
communication,
while
also
proposing
potential
new
functions
for
these
vesicles.
Journal of Nanobiotechnology,
Journal Year:
2025,
Volume and Issue:
23(1)
Published: April 20, 2025
Migrasomes
are
newly
identified
organelles
that
were
first
discovered
in
2015.
Since
then,
their
biological
structure,
formation
process,
and
physiological
functions
have
been
gradually
elucidated.
Research
recent
years
has
expanded
our
understanding
of
these
aspects,
highlighting
significance
various
pathological
processes.
found
to
play
crucial
roles
normal
functions,
including
embryonic
development,
vascular
homeostasis,
material
transport,
mitochondrial
quality
control.
Additionally,
emerging
evidence
suggests
involvement
diseases;
however,
clinical
research
on
remains
limited.
Current
studies
indicate
migrasomes
may
contribute
disease
pathogenesis
hold
potential
for
diagnostic
therapeutic
applications.
This
review
consolidates
existing
migrasomes,
focusing
role
mechanisms
use
medical
By
examining
structure
function,
this
aims
generate
insights
encourage
further
research,
ultimately
contributing
advancements
prevention
treatment.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: May 15, 2025
Migrasomes
are
newly
discovered
extracellular
organelles
released
by
migrating
cells,
such
as
immune
tumor
and
other
special
functional
cells
like
podocytes
embryonic
cells.
They
contain
a
diverse
array
of
constituents,
including
proteins,
lipids,
RNA
which
can
be
to
the
designated
location
activate
surrounding
thereby
facilitating
intercellular
communication
signal
transduction.
Since
then,
our
understanding
mechanism
function
migrasomes
has
expanded
exponentially,
with
recent
evidence
indicating
they
involved
in
various
physiological
pathological
processes,
particularly
regulation.
Furthermore,
methods
techniques
for
extracting,
detecting,
characterizing
constantly
advancing.
Herein,
we
summarize
current
their
key
roles
modulating
responses,
well
prospective
challenges
clinical
application,
aiming
provide
novel
insights
into
emerging
organelles.
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(31)
Published: Aug. 27, 2024
Decellularized
adipose-derived
matrix
(DAM)
has
emerged
as
a
promising
biomaterial
for
soft
tissue
reconstruction.
However,
due
to
lack
of
research
on
its
complex
composition,
the
understanding
key
components
in
DAM
remains
limited,
leading
inconsistent
adipogenic
properties
and
challenges
optimizing
preparation
methods
purposefully.
In
this
study,
it
is
proposed
first
time
that
comprises
two
distinct
components:
hydrophilic
(H-DAM)
lipophilic
(L-DAM),
each
with
markedly
different
effects
fat
regeneration.
It
confirmed
H-DAM
component
inducing
regeneration
enhanced
cell-cell
cell-scaffold
interactions,
primarily
mediated
by
Hedgehog
signaling
pathway.
contrast,
L-DAM
exhibits
poor
cell
adhesion
contains
more
antigenic
components,
higher
immunoinflammatory
response
reduced
adipogenesis.
addition,
found
intracellular
proteins,
which
are
abundant
H-DAM,
can
be
retained
beneficial
their
hydrophilicity,
contrary
conventional
view
they
shall
removed.
Accordingly,
purified
bioscaffold
unprecedented
efficacy
immunogenicity.
This
finding
provides
insights
developing
scaffolds
promotes
realization
xenotransplantation.
The FASEB Journal,
Journal Year:
2024,
Volume and Issue:
38(22)
Published: Nov. 18, 2024
Fat
grafting
is
an
emerging
clinical
technique
to
address
soft
tissue
deficiencies.
This
study
investigates
whether
the
secretory
function
of
beige
adipose
tissue(BeigeAT)
grafts
involved
in
promoting
regeneration
fat
grafting.
In
this
study,
mice
were
randomly
divided
into
white
(WAT)
and
BeigeAT
groups.
Each
type
(0.3
mL)
was
transplanted
respective
groups,
samples
harvested
at
2,
4,
12
week.
Subsequently,
further
three
group,
with
CXCL13
treatment
TAK-779
investigate
role
transplants.
Graft
retention
rate,
vascularization,
fibrosis
levels
compared
among
Compared
WAT
transplants,
transplants
exhibited
moderate
inflammation,
enhanced
revascularization,
reduced
fibrosis,
increased
infiltration
M2
macrophages
endothelial
progenitor
cells
early
stages
following
expression
significantly
higher
week
post-grafting.
Additionally,
modulation
affected
cells.
However,
superior
rates
groups
after
weeks
achieve
improved
through
CXCL13-induced