Proteomics Suggests the Role of Cxcl12 Secreted by Hucmscs in the Treatment of Lipopolysaccharide-Acute Lung Injury
Jinfeng Cui,
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Xiaozhi Wang,
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Liqing Luo
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et al.
Published: Jan. 1, 2025
Language: Английский
CD177 neutrophils exacerbate septic lung injury via the NETs/AIM2 pathway: An experimental and bioinformatics study
International Immunopharmacology,
Journal Year:
2025,
Volume and Issue:
151, P. 114292 - 114292
Published: Feb. 24, 2025
Language: Английский
Targeting neutrophil dysfunction in acute lung injury: insights from active components of Chinese medicine
Saiya Ye,
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Lin Ma,
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Yayun Chi
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et al.
Phytomedicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 156664 - 156664
Published: March 1, 2025
Language: Английский
Serum ferritin is a superior biomarker for evaluating disease activity and kidney injury compared with C-reactive protein in anti-neutrophil cytoplasmic antibody-associated vasculitis
Liyuan Xie,
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Xinyun Qiu,
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Yu-Nan Li
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et al.
Clinical Rheumatology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 2, 2025
Language: Английский
Wogonin alleviates sepsis-induced acute lung injury by modulating macrophage polarization through the SIRT1-FOXO1 pathways
Jinlin Ge,
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Huanhuan Yang,
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Ningning Yu
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et al.
Tissue and Cell,
Journal Year:
2024,
Volume and Issue:
88, P. 102400 - 102400
Published: May 5, 2024
Sepsis-induced
acute
lung
injury
is
a
common
and
severe
complication
of
sepsis,
for
which
effective
treatments
are
currently
lacking.
Previous
studies
have
demonstrated
the
influence
wogonin
in
treating
(ALI).
However,
its
precise
mechanism
action
remains
unclear.
To
delve
deeper
into
mechanisms
underlying
wogonin's
impacts
sepsis-induced
injury,
we
established
mouse
sepsis
model
through
cecal
ligation
puncture
conducted
further
cell
experiments
using
lipopolysaccharide-treated
MH-S
MLE-12
cells
to
explore
potential
ALI.
Our
results
revealed
that
significantly
increased
survival
rate
mice,
alleviated
pulmonary
pathological
damage
inflammatory
infiltration,
activated
SIRT1-FOXO1
pathway.
Additionally,
suppressed
release
pro-inflammatory
factors
by
M1
macrophages
induced
activation
M2
anti-inflammatory
factors.
Further
vitro
confirmed
effectively
inhibited
macrophage
polarization
pathway,
thereby
mitigating
changes
caused
In
summary,
our
study
regulated
M1/M2
attenuating
response
improving
This
discovery
provided
solid
mechanistic
foundation
therapeutic
use
ALI,
shedding
new
light
on
strategies
treatment
Language: Английский
ROS responsive nanozyme loaded with STING silencing for the treatment of sepsis-induced acute lung injury
Y. F. Zhang,
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Lingyang Chen,
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Lin Feng
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et al.
Toxicology and Applied Pharmacology,
Journal Year:
2024,
Volume and Issue:
493, P. 117155 - 117155
Published: Nov. 12, 2024
Language: Английский
Neutrophil extracellular traps promote the activation of the NLRP3 inflammasome and PBMCs pyroptosis via the ROS-dependent signaling pathway in Kawasaki disease
International Immunopharmacology,
Journal Year:
2024,
Volume and Issue:
145, P. 113783 - 113783
Published: Dec. 7, 2024
Language: Английский
Identification of sepsis-related genes by integrating eQTL data with Mendelian randomization analysis
Chao Wen,
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Dongliang Yang,
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Hongyan Guo
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et al.
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 24, 2024
Abstract
Background
Sepsis
is
defined
as
a
life-threatening
organ
dysfunction
caused
by
dysfunctional
host
response
to
infection
and
associated
with
high
mortality.
However,
there
currently
no
effective
treatment
strategy
for
sepsis.
Methods
We
obtained
GSE263789,
GSE54514
GSE66099
from
the
Gene
Expression
Omnibus
(GEO)
database
selected
differentially
expressed
genes
(DEGs).
extracted
expression
quantitative
trait
loci
(eQTL)
exposure
sepsis
GWAS
outcome
IEU
Open
database.
MR
analysis
was
used
assess
causality
between
eQTL
The
overlapping
of
DEGs
significant
were
identified
key
genes.
Enrichment
immune
cell
infiltration
performed
verified
in
validation
cohort.
Results
18
sepsis-related
genes,
including
11
up-regulated
(SEMA4A,
LRPAP1,
FAM89B,
TOMM40L,
SLC22A15,
MACF1,
MCTP2,
NTSR1,
PNKD,
ACTR10,
CPNE3)
7
down-regulated
(IKZF3,
TNFRSF25,
HDC,
HCP5,
LYRM4,
TFAM,
RPS15A).
analyses
showed
that
these
are
mainly
involved
biological
processes
related
inflammatory
response.
Compared
healthy
controls,
abundance
neutrophils
activated
mast
cells
increased
group.
Most
correlated
cells,
neutrophils,
CD8
T
resting
NK
plasma
memory
B
macrophage
subtypes.
Conclusion
By
combining
bioinformatics
analysis,
we
sepsis,
enhancing
our
understanding
genetic
pathogenesis
providing
new
insights
into
therapeutic
targets
Language: Английский
CircIRAK3 Promotes Neutrophil Extracellular Trap Formation by Improving the Stability of ELANE mRNA in Sepsis
Yao Lu,
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Huang Wu,
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Yuanyuan Luo
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et al.
Inflammation,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 21, 2024
Language: Английский