Nuclear receptor subfamily 4 group A member 1 promotes myocardial ischemia/reperfusion injury through inducing mitochondrial fission factor-mediated mitochondrial fragmentation and inhibiting FUN14 domain containing 1-depedent mitophagy
Junyan Wang,
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Haowen Zhuang,
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Lianqun Jia
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et al.
International Journal of Biological Sciences,
Journal Year:
2024,
Volume and Issue:
20(11), P. 4458 - 4475
Published: Jan. 1, 2024
This
study
investigated
the
mechanism
by
which
NR4A1
regulates
mitochondrial
fission
factor
(Mff)-related
and
FUN14
domain
1
(FUNDC1)-mediated
mitophagy
following
cardiac
ischemia-reperfusion
injury(I/R).
Our
findings
showed
that
damage
regulation
was
positively
correlated
with
pathological
pan-apoptosis
of
myocardial
cell
mitochondria.
Compared
wild-type
mice
(WT),
NR4A1-knockout
exhibited
resistance
to
injury
fission,
characterized
activation.
Results
increased
expression
level,
activating
mediated
Mff
restoring
phenotype
FUNDC1.
The
inactivation
FUNDC1
phosphorylation
could
not
mediate
normalization
in
a
timely
manner,
leading
an
excessive
stress
response
unfolded
proteins
imbalance
homeostasis.
process
disrupted
quality
control
network,
accumulation
damaged
mitochondria
activation
pan-apoptotic
programs.
data
indicate
is
novel
critical
target
I/R
exertsand
negative
regulatory
effects
Mff-mediated
mito-fission
inhibiting
FUNDC1-mediated
mitophagy.
Targeting
crosstalk
balance
between
NR4A1-Mff-FUNDC1
potential
approach
for
treating
I/R.
Language: Английский
A novel PDE4 inhibitor ZX21011 alleviates neuronal apoptosis by decreasing GSK3β-mediated Drp1 Ser616 phosphorylation in cerebral ischemia reperfusion
Huizhen Wen,
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Xingxing Tu,
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Fulan Luo
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et al.
Chemico-Biological Interactions,
Journal Year:
2025,
Volume and Issue:
unknown, P. 111405 - 111405
Published: Jan. 1, 2025
Language: Английский
Adaptive Divergence and Functional Convergence: The Evolution of Pulmonary Gene Expression in Amphibians of the Qingzang Plateau
Liming Chang,
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Wei Zhu,
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Qiheng Chen
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et al.
Molecular Ecology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 3, 2025
ABSTRACT
The
Qingzang
Plateau,
with
its
harsh
environmental
conditions—low
oxygen,
high
ultraviolet
radiation
and
significant
temperature
fluctuations—demands
specialised
adaptations
for
survival.
While
genetic
have
been
extensively
studied,
gene
expression's
role
in
amphibian
adaptation
to
elevations
remains
understudied.
This
study
analysed
pulmonary
expression
119
amphibians
across
the
plateau
explore
how
factors
shape
evolution.
Transcriptomic
analyses
revealed
interspecies
variation,
driven
by
like
temperature,
oxygen
levels,
UVB
precipitation.
Principal
Component
Mantel
found
no
correlation
between
divergence
distance.
Instead,
species‐specific
traits
pressures
were
pivotal
shaping
patterns.
PERMANOVA
analysis
showed
had
varying
impacts
on
species.
For
instance,
Bufo
gargarizans
exhibited
a
strong
response
multiple
factors,
while
Scutiger
boulengeri
was
less
influenced,
reflecting
diverse
adaptive
strategies.
Functional
enrichment
highlighted
convergence
key
biological
processes,
such
as
energy
metabolism,
apoptosis
autophagy,
despite
differences.
These
processes
are
critical
surviving
plateau's
extremes.
findings
suggest
that
evolution
Plateau
is
shaped
both
diversity
pressures.
Although
profiles
vary,
they
converge
essential
functions,
offering
insights
into
mechanisms
extreme
environments.
Language: Английский
Preconditioning with Ginsenoside Rg3 mitigates cardiac injury induced by high-altitude hypobaric hypoxia exposure in mice by suppressing ferroptosis through inhibition of the RhoA/ROCK signaling pathway
Junling Liu,
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Caixia Pei,
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Nan Jia
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et al.
Journal of Ethnopharmacology,
Journal Year:
2024,
Volume and Issue:
337, P. 118861 - 118861
Published: Sept. 24, 2024
Language: Английский
Decreased ATF5 level contributes to improved mitochondrial function in oocytes exposed to vitrification stress
Guizhen Zhou,
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Aiju Liu,
No information about this author
Jiachen Bai
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et al.
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: Sept. 20, 2024
Background
Mitochondrial
unfolded
protein
response
(mtUPR)
plays
an
essential
role
in
the
of
mitochondria
to
stress-induced
damage.
Activating
transcription
factor
5
(ATF5)
can
help
sustain
mitochondrial
function
and
regulate
organelle
recovery
under
stress.
Vitrification
is
a
stressor
that
disrupts
activity
cell
homeostasis.
However,
little
known
about
ATF5
extreme
biophysical
chemical
stresses
during
oocyte
vitrification.
Methods
The
expression
mtUPR
biomarkers
were
measured
fresh
vitrified
oocytes.
Subsequently,
oocytes
with
deficiency
constructed
by
siRNA
microinjection,
development
analyzed
Furthermore,
transcriptome
analysis
was
performed
uncover
molecular
network
regulated
Results
In
present
study,
membrane
potential
ATP
levels
decreased
knockdown
oocytes,
line
phenotypes
observed
addition,
resulted
temperature,
reduced
levels,
abnormal
dynamics
(fusion
fission),
increased
autophagy.
Subsequent
experiments
indicated
suppressed
knockdown.
Interestingly,
aberrantly
upregulated
exposed
vitrification
Reduced
homeostatic
level
led
accumulated
potential.
Moreover,
germinal
vesicle
breakdown
(GVBD)
rate
detected
after
vitro
maturation.
Transcriptome
revealed
involved
stress
response,
maturation
through
cAMP-PKA
PI3K/AKT
pathways.
Discussion
Our
findings
indicate
initiated
stimuli,
downregulated
state
contributes
improved
results
highlight
crucial
regulation
mediating
mtUPR.
Language: Английский