The Journal of Cell Biology,
Journal Year:
2025,
Volume and Issue:
224(4)
Published: Jan. 29, 2025
Sphingolipids
serve
as
building
blocks
of
membranes
to
ensure
subcellular
compartmentalization
and
facilitate
intercellular
communication.
How
cell
type–specific
lipid
compositions
are
achieved
what
is
their
functional
significance
in
tissue
morphogenesis
maintenance
has
remained
unclear.
Here,
we
identify
a
stem
cell–specific
role
for
ceramide
synthase
4
(CerS4)
orchestrating
fate
decisions
skin
epidermis.
Deletion
CerS4
prevents
the
proper
development
adult
hair
follicle
bulge
(HFSC)
compartment
due
altered
differentiation
trajectories.
Mechanistically,
HFSC
defects
arise
from
an
imbalance
key
ceramides
derivate
sphingolipids,
resulting
hyperactivation
noncanonical
Wnt
signaling.
This
impaired
establishment
leads
disruption
architecture
barrier
function,
ultimately
triggering
T
helper
2–dominated
immune
infiltration
resembling
human
atopic
dermatitis.
work
uncovers
fundamental
state–specific
sphingolipid
profile
homeostasis
maintaining
intact
barrier.
Bioactive Materials,
Journal Year:
2023,
Volume and Issue:
34, P. 51 - 63
Published: Dec. 14, 2023
Effective
bone
regeneration
through
tissue
engineering
requires
a
combination
of
osteogenic
progenitors,
osteoinductive
biofactors
and
biocompatible
scaffold
materials.
Mesenchymal
stem
cells
(MSCs)
represent
the
most
promising
seed
for
engineering.
As
multipotent
that
can
self-renew
differentiate
into
multiple
lineages
including
fat,
MSCs
be
isolated
from
numerous
tissues
exhibit
varied
differentiation
potential.
To
identify
an
optimal
progenitor
cell
source
engineering,
we
analyzed
proliferative
activity
potential
four
commonly-used
mouse
MSC
sources,
immortalized
embryonic
fibroblasts
(iMEF),
marrow
stromal
(imBMSC),
calvarial
mesenchymal
progenitors
(iCAL),
adipose-derived
(iMAD).
We
found
iMAD
exhibited
highest
adipogenic
capabilities
upon
BMP9
stimulation
Oncogene,
Journal Year:
2024,
Volume and Issue:
43(9), P. 624 - 635
Published: Jan. 5, 2024
Abstract
Hepatocellular
carcinoma
(HCC)
is
one
of
the
leading
contributors
to
cancer-related
mortality
worldwide.
Nop2/Sun
domain
family
member
5
(NSUN5),
a
conserved
RNA
5-methylcytosine
methyltransferase,
conventionally
recognized
as
oncogenic.
However,
its
role
in
HCC
development
remains
unknown.
In
this
study,
we
observed
remarkable
upregulation
NSUN5
expression
both
tumor
tissues
from
patients
with
HCC,
establishing
correlation
unfavorable
clinical
outcomes.
knockdown
and
overexpression
significantly
inhibited
promoted
cell
proliferation,
respectively.
Additionally,
employing
combination
methylated
immunoprecipitation
sequencing
(MeRIP-seq)
RIP-seq
techniques,
identified
zinc
finger
BED
domain-containing
protein
3
(ZBED3)
novel
downstream
target
NSUN5.
found
that
ZBED3
counteracted
tumor-suppressing
effect
simultaneously
reversed
inhibition
Wnt/β-catenin
signaling
pathway.
summary,
elucidated
oncogenic
ZBED3/Wnt/β-catenin
pathway
target.
This
study
provides
therapeutic
for
further
treatment.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
204, P. 107200 - 107200
Published: May 6, 2024
Targeting
specific
molecular
drivers
of
tumor
growth
is
a
key
approach
in
cancer
therapy.
Among
these
targets,
the
low-density
lipoprotein
receptor-related
protein
6
(LRP6),
vital
component
Wnt
signaling
pathway,
has
emerged
as
an
intriguing
candidate.
As
cell-surface
receptor
and
co-receptor,
LRP6
frequently
overexpressed
various
types,
implicating
its
pivotal
role
driving
progression.
The
pursuit
target
for
treatment
gained
substantial
traction,
offering
promising
avenue
therapeutic
intervention.
Here,
this
comprehensive
review
explores
recent
breakthroughs
our
understanding
LRP6's
functions
underlying
mechanisms,
providing
profound
discussion
involvement
pathogenesis
drug
resistance.
Importantly,
we
go
beyond
discussing
by
diverse
potential
approaches
targeting
enigmatic
protein.
These
encompass
wide
spectrum,
including
pharmacological
agents,
natural
compounds,
non-coding
RNAs,
epigenetic
factors,
proteins,
peptides
that
modulate
expression
or
disrupt
interactions.
In
addition,
also
discussed
challenges
associated
with
developing
inhibitors
their
advantages
over
inhibitors,
well
drugs
have
entered
phase
II
clinical
trials.
By
shedding
light
on
innovative
strategies,
aim
to
underscore
significance
valuable
multifaceted
treatment,
igniting
enthusiasm
further
research
facilitating
translation
into
applications.
Trends in Cell Biology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
HighlightsA
cell
possesses
competency
if
it
expresses
specific
receptors
and
can
thus
react
to
complementary
signalling
ligands.Signalling
ligands
be
disseminated
via
filopodia
called
cytonemes
exovesicles
such
as
exosomes.Cytonemes
exosomes
also
transport
receiving
cells.Upon
acquiring
transferred
receptors,
cells
the
appropriate
signal
acquire
adoptive
competency.AbstractCellular
communication
through
dissemination
of
molecules
is
vital
for
tissue
organisation
homeostasis.
The
mechanisms
spreading
include
binding-protein-assisted
transport,
long
membrane
protrusions
known
cytonemes,
exovesicles.
Recent
research
indicates
that
not
only
but
facilitate
regulated
distribution
thereby
enabling
transduction
in
lacking
endogenous
receptors.
This
mechanism
allows
non-responsive
temporarily
ability
respond
ligands.
review
explores
our
understanding
ligand
receptor
dispersal,
offering
fresh
insights
into
fundamental
concept
cellular
competence.
Notably,
these
findings
may
have
significant
implications
diseases
their
associated
therapeutic
targets,
highlighting
urgency
importance
this
area.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(2), P. 228 - 228
Published: Jan. 12, 2025
Triple-negative
breast
cancer
(TNBC)
is
one
of
the
most
difficult
subtypes
to
treat
due
its
distinct
clinical
and
molecular
characteristics.
Patients
with
TNBC
face
a
high
recurrence
rate,
an
increased
risk
metastasis,
lower
overall
survival
compared
other
subtypes.
Despite
advancements
in
targeted
therapies,
traditional
chemotherapy
(primarily
using
platinum
compounds
taxanes)
continues
be
standard
treatment
for
TNBC,
often
limited
long-term
efficacy.
tumors
are
heterogeneous,
displaying
diverse
mutation
profile
considerable
chromosomal
instability,
which
complicates
therapeutic
interventions.
The
development
chemoresistance
frequently
associated
process
epithelial–mesenchymal
transition
(EMT),
during
epithelial
tumor
cells
acquire
mesenchymal-like
phenotype.
This
shift
enhances
metastatic
potential,
while
simultaneously
reducing
effectiveness
chemotherapeutics.
It
has
also
been
suggested
that
EMT
plays
central
role
stem
cells.
Hence,
there
growing
interest
exploring
small-molecule
inhibitors
target
as
future
strategy
overcoming
resistance
improving
outcomes
patients
TNBC.
review
focuses
on
progression
drug
emphasis
these
processes.
We
present
TNBC-specific
EMT-related
features,
key
protein
markers,
various
signaling
pathways
involved.
discuss
important
mechanisms
factors
related
within
context
EMT,
highlighting
improve
patients’
outcomes.
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: July 21, 2023
Hepatocellular
carcinoma
(HCC)
is
one
of
the
deadliest
cancers
due
to
multifocal
development
and
distant
metastasis
resulting
from
late
diagnosis.
Consequently,
new
approaches
HCC
diagnosis
treatment
are
required
reduce
mortality
rates.
A
large
body
evidence
suggests
that
non-coding
RNAs
(ncRNAs)
important
in
cancer
initiation
progression.
Cancer
cells
release
many
these
ncRNAs
into
blood
or
urine,
enabling
their
use
as
a
diagnostic
tool.
Circular
(CircRNAs)
members
regulate
cell
expansion,
migration,
metastasis,
chemoresistance
through
different
mechanisms
such
Wnt/β-catenin
Signaling
pathway.
The
pathway
plays
prominent
roles
several
biological
processes
including
organogenesis,
stem
regeneration,
survival.
Aberrant
signaling
both
pathways
mentioned
above
could
affect
progression
cancers,
HCC.
Based
on
studies
investigated
current
review,
circRNAs
have
an
effect
formation
by
sponging
miRNAs
RNA-binding
proteins
(RBPs)
regulating
Therefore,
circRNAs/miRNAs
RBPs/Wnt/β-catenin
be
considered
promising
prognostic
therapeutic
targets
Journal of Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12(3), P. 20 - 20
Published: Aug. 2, 2024
The
formation
of
embryonic
axes
is
a
critical
step
during
animal
development,
which
contributes
to
establishing
the
basic
body
plan
in
each
particular
organism.
Wnt
signaling
pathways
play
pivotal
roles
this
fundamental
process.
Canonical
that
dependent
on
β-catenin
regulates
patterning
dorsoventral,
anteroposterior,
and
left–right
axes.
Non-canonical
independent
modulates
cytoskeletal
organization
coordinate
cell
polarity
changes
asymmetric
movements.
It
now
well
documented
components
these
biochemically
functionally
interact
mediate
cell–cell
communications
instruct
cellular
polarization
breaking
symmetry.
dysfunction
disrupts
axis
specification
proper
tissue
morphogenesis,
mutations
pathway
genes
are
associated
with
birth
defects
humans.
This
review
discusses
regulatory
by
focusing
vertebrate
models.
highlights
current
progress
decoding
conserved
mechanisms
underlying
establishment
asymmetry
along
three
primary
By
providing
an
in-depth
analysis
canonical
non-canonical
regulating
fates
behaviors,
work
offers
insights
into
intricate
processes
contribute
setting
up
embryos.
Journal of Neuroinflammation,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: Oct. 19, 2024
The
blood-brain
barrier
(BBB)
is
a
critical
interface
that
maintains
the
central
nervous
system
homeostasis
by
controlling
exchange
of
substances
between
blood
and
brain.
Disruption
BBB
plays
vital
role
in
development
neuroinflammation
neurological
dysfunction
sepsis,
but
mechanisms
which
becomes
disrupted
during
sepsis
are
not
well
understood.
Here,
we
induced
endotoxemia,
major
type
mice
intraperitoneal
injection
lipopolysaccharide
(LPS).
LPS
acutely
increased
permeability,
activated
microglia,
heightened
inflammatory
responses
brain
endothelium
parenchyma.
Concurrently,
or
proinflammatory
cytokines
NF-κB
pathway,
inhibiting
Wnt/β-catenin
signaling
endothelial
cells
vitro
vivo.
Cell
culture
study
revealed
p65
directly
interacted
with
β-catenin
to
suppress
signaling.
Pharmacological
pathway
inhibition
restored
activity
mitigated
disruption
septic
mice.
Furthermore,
genetic
pharmacological
activation
substantially
alleviated
LPS-induced
leakage
neuroinflammation,
while
conditional
ablation
Wnt7a/7b
co-receptor
Gpr124
exacerbated
caused
LPS.
Mechanistically,
rectified
reduced
expression
levels
tight
junction
protein
ZO-1
transcytosis
suppressor
Mfsd2a
both
paracellular
transcellular
permeability
BBB.
Our
findings
demonstrate
endotoxemia-associated
systemic
inflammation
decreases
through
activating
resulting
acute
neuroinflammation.
Targeting
may
offer
promising
therapeutic
strategy
for
preserving
integrity
treating
sepsis.