Molecular Medicine Reports,
Journal Year:
2024,
Volume and Issue:
31(1)
Published: Nov. 5, 2024
Long
non‑coding
RNAs
serve
a
crucial
role
in
autophagy
of
vascular
smooth
muscle
cells
(VSMCs).
The
present
study
aimed
to
investigate
the
effect
small
nucleolar
RNA
host
gene
1
(SNHG1)
on
VSMCs
and
associated
underlying
mechanisms.
Rapamycin
was
used
induce
effects
SNHG1
proliferation
migration
change
phenotype
were
tested
following
overexpression
silencing
SNHG1.
target
predicted
validated.
SNHG1‑regulated
via
C‑type
lectin
domain
family
7
member
A
(CLEC7A)
determined
by
combined
CLEC7A.
Rapamycin‑induced
changed
cell
from
contractile
synthetic,
with
decreased
expression
α‑smooth
actin
protein
22a
increased
osteopontin.
Overexpression
caused
same
while
opposite
observed
silencing.
promoted
VSMCs.
CLEC7A
identified
as
direct
binding
relationship
between
them
confirmed
immunoprecipitation
pull‑down
assays.
both
during
reduced
this
In
conclusion,
autophagy.
promotes
conversion
synthetic
facilitating
expression.
Journal of Oral Rehabilitation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 26, 2024
ABSTRACT
Background
Early
treatment
of
mandibular
advancement
device
(MAD)
reverses
the
abnormal
changes
resulting
from
obstructive
sleep
apnoea
(OSA),
but
underlying
mechanism
is
not
clear.
We
analysed
genioglossus
function
before
and
after
MAD
in
OSA
rabbits
explored
mitochondrial
autophagy.
Methods
Eighteen
male
New
Zealand
were
randomised
into
three
groups:
control
group,
Group
OSA,
MAD.
After
successful
modelling,
all
animals
induced
supine
positions
for
4–6
h
per
day
8
weeks.
Cone
beam
computed
tomography
(CBCT)
polysomnography
(PSG)
performed
to
record
conditions.
The
contractile
force
levels
LC3‐I,
LC3‐II,
Beclin‐1,
PINK1
Parkin
detected
groups.
In
vitro,
C2C12
myoblast
cells
cultured
under
normoxic
or
hypoxic
conditions
24
h,
then
structure
accumulation
autolysosomes
by
transmission
electron
microscopy
(TEM).
Results
tension
was
significantly
lower
than
that
group.
ratio
LC3II/LC3I
higher
And
tended
be
normal
treatment.
disrupted,
number
increased
hypoxia.
Conclusions
may
decrease
increase
level
autophagy
caused
OSA.
mediated
PINK1/Parkin
pathway
rabbits.
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: Dec. 8, 2023
Autophagy,
a
crucial
cellular
mechanism
responsible
for
degradation
and
recycling
of
intracellular
components,
is
modulated
by
an
intricate
network
molecular
signals.
Its
paradoxical
involvement
in
oncogenesis,
acting
as
both
tumor
suppressor
promoter,
has
been
underscored
recent
studies.
Central
to
this
regulatory
are
the
epigenetic
modifications
DNA
RNA
methylation,
notably
presence
N6-methyldeoxyadenosine
(6mA)
genomic
N6-methyladenosine
(m6A)
eukaryotic
mRNA.
The
6mA
modification
adds
extra
dimension
regulation,
potentially
impacting
transcriptional
dynamics
genes
linked
autophagy
and,
especially,
cancer.
Conversely,
m6A
modification,
governed
methyltransferases
demethylases,
influences
mRNA
stability,
processing,
translation,
affecting
central
autophagic
pathways.
As
we
delve
deeper
into
complexities
importance
these
methylation
grows
more
evident.
interplay
6mA,
m6A,
points
layered
mechanism,
illuminating
reactions
range
conditions.
This
review
delves
nexus
between
their
influence
on
cancer
contexts.
By
closely
examining
markers,
underscore
promise
therapeutic
avenues,
suggesting
novel
approaches
intervention
through
modulation.
Physiological Research,
Journal Year:
2024,
Volume and Issue:
unknown, P. 189 - 203
Published: April 30, 2024
This
comprehensive
review
explores
the
physiological
and
pathophysiological
significance
of
VPS13A,
a
protein
encoded
by
VPS13A
gene.
The
gene
is
associated
with
Chorea-acanthocytosis
(ChAc),
rare
hereditary
neurodegenerative
disorder.
covers
essential
aspects,
beginning
genetics
highlighting
its
role
in
pathogenesis
ChAc,
addressing
spectrum
genetic
variants
involved.
It
delves
into
structure
function
protein,
emphasizing
presence
various
tissues
potential
involvement
trafficking
lipid
homeostasis.
Molecular
functions
brain
tissue
other
cell
types
or
respect
to
their
cytoskeletal
regulation
autophagy
are
explored.
Finally,
it
intriguing
link
between
mutations,
imbalances,
neurodegeneration,
shedding
light
on
future
research
directions.
Overall,
this
serves
as
resource
for
understanding
pivotal
health
disease,
particularly
context
ChAc.
Key
words:
Chorein
,
Tumor,
Actin,
Microfilament,
Gene
expression,
Chorea-acanthocytosis.
Journal of Dental Sciences,
Journal Year:
2024,
Volume and Issue:
20(1), P. 487 - 501
Published: May 15, 2024
Heat
stress
is
essential
for
improving
the
efficacy
of
mesenchymal
stem
cell
(MSC)-based
regeneration
medicine.
However,
it
still
unclear
whether
and
how
heat
influences
differentiation
cells
from
apical
papilla
(SCAPs).
This
research
aimed
to
explore
potential
mechanism
glucose-regulated
protein
78
(GRP78)
in
regulating
under
SCAPs.
The
proliferation
ability
was
assessed
using
5-Ethynyl-2'-
deoxyuridine
(EdU)
assay,
counting
kit
assay
(CCK-8),
flow
cytometry
(FCM).
osteogenic
odontogenic
capacities
were
investigated
through
Western
blot,
quantitative
reverse
transcription
polymerase
chain
reaction
(qRT-PCR),
alkaline
phosphatase
(ALP)
staining
activity
alizarin
red
S
(ARS)
staining,
as
well
immunofluorescence
staining.
blot
transmission
electron
microscopy
(TEM)
used
detect
autophagy.
enhanced
SCAPs,
but
did
not
significantly
affect
proliferation.
Besides,
GRP78
has
been
confirmed
modulate
induced
by
stress.
Autophagy
triggered
while
knockdown
or
inhibitor
autophagy
suppressed
differentiation.
induces
SCAPs
GRP78-mediated
Molecular Medicine Reports,
Journal Year:
2024,
Volume and Issue:
31(1)
Published: Nov. 5, 2024
Long
non‑coding
RNAs
serve
a
crucial
role
in
autophagy
of
vascular
smooth
muscle
cells
(VSMCs).
The
present
study
aimed
to
investigate
the
effect
small
nucleolar
RNA
host
gene
1
(SNHG1)
on
VSMCs
and
associated
underlying
mechanisms.
Rapamycin
was
used
induce
effects
SNHG1
proliferation
migration
change
phenotype
were
tested
following
overexpression
silencing
SNHG1.
target
predicted
validated.
SNHG1‑regulated
via
C‑type
lectin
domain
family
7
member
A
(CLEC7A)
determined
by
combined
CLEC7A.
Rapamycin‑induced
changed
cell
from
contractile
synthetic,
with
decreased
expression
α‑smooth
actin
protein
22a
increased
osteopontin.
Overexpression
caused
same
while
opposite
observed
silencing.
promoted
VSMCs.
CLEC7A
identified
as
direct
binding
relationship
between
them
confirmed
immunoprecipitation
pull‑down
assays.
both
during
reduced
this
In
conclusion,
autophagy.
promotes
conversion
synthetic
facilitating
expression.