Sodium propionate protects against bronchopulmonary dysplasia by inhibiting IL-17-mediated apoptosis of alveolar epithelial cells
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: April 5, 2025
Sodium
propionate
(SP)
has
been
shown
to
enhance
alveolar
growth
retardation
in
Bronchopulmonary
Dysplasia
(BPD),
but
the
mechanism
remains
unclear.
The
aim
of
this
study
is
explore
potential
SP
treatment
BPD
by
utilizing
animal
and
cell
models
along
with
bioinformation
analysis.
Neonatal
mice
were
exposed
either
air
(21%
O2)
or
hyperoxia
(85%
from
first
day
after
birth
establish
model.
neonatal
intraperitoneally
injected
normal
saline
(control
group)
(500
mg/kg,
8
14.
significantly
reduced
inflammatory
condition
septal
thickening,
decreased
fusion
mitigated
weight
loss
mice.
ELISA
results
demonstrated
that
inhibited
secretion
IL-17,
IL-6
TNFα.
Transcriptome
analysis
confirmed
IL-17
signaling
pathway
closely
related
therapeutic
effects
on
BPD.
In
addition,
MX2,
MMP10,
IL-11,
ZMAT4
SEC1
genes
identified
as
key
targets
involved
treating
Meanwhile,
mouse
epithelial
cells,
apoptosis
was
induced
hyperoxia,
it
following
intervention.
expression
genes:
IL-17A,
IL-6,
TNFα
cox2
treated
cells
conclusion,
through
transcriptome
analysis,
experiments,
we
explored
role
sodium
attenuating
a
model
pathway.
Language: Английский
dNTP depletion and beyond: the multifaceted nature of SAMHD1-mediated viral restriction
Journal of Virology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
ABSTRACT
SAMHD1
is
a
dNTPase
of
mammalian
cells.
In
2011,
was
found
to
be
host
restriction
factor
against
retroviruses
through
dNTP
reduction.
Recent
research
provides
evidence
that
the
antiviral
mechanisms
cannot
explained
solely
by
its
activity.
Instead,
versatility
SAMHD1-mediated
various
viruses
suggests
extend
beyond
depletion.
This
explains
multifaceted
and
broad
functions
play
significant
role
in
innate
immunity.
Language: Английский
CRL4-DCAF1 Ubiquitin Ligase Dependent Functions of HIV Viral Protein R and Viral Protein X
Ashley Dobransky,
No information about this author
Mary Root,
No information about this author
Nicholas Hafner
No information about this author
et al.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(8), P. 1313 - 1313
Published: Aug. 17, 2024
The
Human
Immunodeficiency
Virus
(HIV)
encodes
several
proteins
that
contort
the
host
cell
environment
to
promote
viral
replication
and
spread.
This
is
often
accomplished
through
hijacking
of
cellular
ubiquitin
ligases.
These
reprogrammed
complexes
initiate
or
enhance
ubiquitination
may
otherwise
act
restrain
replication.
Ubiquitination
target
alter
protein
function
proteasome-dependent
destruction.
HIV
Viral
Protein
R
(Vpr)
related
HIV-2
X
(Vpx),
engage
CRL4-DCAF1
ligase
complex
numerous
proteins.
In
this
review
we
describe
its
interactions
with
Vpr
Vpx.
We
additionally
summarize
targeted
by
association
as
well
observed
hypothesized
impact
on
HIV.
Language: Английский
The avengers: SAMHD1 cooperates with MX2/MxB to defend against HIV-1
Zhi Wan,
No information about this author
Gang Zhong,
No information about this author
Huiqing Wang
No information about this author
et al.
mBio,
Journal Year:
2024,
Volume and Issue:
15(10)
Published: Sept. 6, 2024
SAMHD1
is
an
intrinsic
limiting
factor
that
effectively
prevents
HIV-1
infection
in
macrophages,
dendritic
cells,
and
resting
CD4+
T
cells.
Extensive
studies
have
underscored
the
indispensable
role
of
dNTPase
activity
its
antiviral
function
by
primarily
depleting
dNTPs
quiescent
thereby
impeding
cDNA
synthesis.
However,
recent
advancements
understanding
posttranslational
modifications
revealed
specific
modification
site
mutants
maintain
their
ability
to
reduce
dNTP
levels
while
impairing
inhibition
replication.
Thus,
precise
anti-HIV-1
mechanism
remains
enigmatic,
necessitating
a
comprehensive
underlying
mechanisms
develop
novel
therapeutic
strategies
targeting
activity.
Recent
findings
Guo
et
al.
shed
light
on
as
core
sensor
suppressing
after
viral
synthesis
through
interaction
with
MX2
(H.
Guo,
W.
Yang,
H.
Li,
J.
al.,
mBio
15:e01363-24,
2024,
https://doi.org/10.1128/mbio.01363-24).
Language: Английский