Neochlorogenic acid ameliorates allergic airway inflammation by suppressing type 2 immunity and upregulating HO-1 expression
International Immunopharmacology,
Journal Year:
2024,
Volume and Issue:
146, P. 113867 - 113867
Published: Dec. 16, 2024
Language: Английский
Eosinophils and pleural macrophages counter regulate IL-33-elicited airway inflammation via the 12/15-lipoxygenase pathway
E. Ito,
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Reika Hayashizaki,
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Tetsuya Hosaka
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et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 17, 2025
Fatty
acid
metabolism
plays
a
crucial
role
in
regulating
airway
inflammation
through
the
synthesis
of
lipid
mediators.
We
have
previously
demonstrated
that
12/15-lipoxygenase
(12/15-LOX
or
Alox15)-derived
mediator
attenuates
IL-33-induced
eosinophilic
mice.
However,
cellular
sources
these
mediators
remain
unclear.
To
identify
sources,
we
used
several
cell
type-specific
conditional
12/15-LOX-deficient
found
eosinophils
and
pleural
macrophages
were
major
12/15-LOX-expressing
types
responsible
for
attenuating
inflammation.
Eosinophils
population
cells
inflamed
lung
tissue.
In
addition,
thoracic
cavity
to
translocate
into
tissue
response
This
study
suggests
cooperatively
regulate
via
12/15-LOX
expression.
Targeting
may
offer
new
therapeutic
strategies
severe
asthma.
Language: Английский
Pulsed 980 nm Near-Infrared Photobiomodulation Attenuates OVA-Induced Allergic Asthma by Modulating Th2 Cytokine Responses and Inflammatory Cell Infiltration
Zhengyi Wu,
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Jia Zhang,
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Qingxiang Gao
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et al.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 6, 2025
Abstract
Photobiomodulation
(PBM)
is
a
non-invasive
therapeutic
strategy
that
uses
specific
light
wavelengths
to
stimulate
cellular
processes
promote
tissue
repair,
reduce
inflammation,
and
alleviate
pain.
In
this
study,
we
evaluated
the
efficacy
of
high-intensity
980
nm
near-infrared
(NIR)
pulsed
laser
in
murine
model
ovalbumin
(OVA)-induced
allergic
asthma.
OVA-sensitized
mice,
typical
features
were
noted,
including
airway
wall
thickening,
significant
peribronchial
perivascular
inflammatory
cell
infiltration,
compressed
alveolar
spaces.
NIR
PBM
treatment
markedly
attenuated
these
histological
changes.
At
molecular
level,
significantly
downregulated
type
2
cytokine
gene
expression,
IL-4,
IL-5
IL-13,
lung
tissue.
Flow
cytometry
analyses
further
revealed
reduced
infiltration
pulmonary
eosinophils
monocytes.
Transcriptomic
profiling
coupled
with
set
enrichment
analysis
(GSEA)
indicated
suppressed
NF-κB-mediated
signaling
while
modulating
Th2-related
responses.
Collectively,
our
findings
demonstrate
effectively
mitigates
key
asthma
model,
supporting
its
potential
as
non-pharmacological,
adjunct
therapy
for
management.
Language: Английский
Eosinophil-Airway Epithelial Cells crosstalk reveals the eosinophils-mediated DUOX1 up-regulation in a murine allergic inflammation setting
Journal of Leukocyte Biology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 24, 2024
Abstract
Blood
and
airway
eosinophilia
represent
markers
for
the
endotype-driven
treatment
of
allergic
asthma.
Little
is
known
on
mechanisms
that
link
eosinophils
epithelial
cells
before
after
these
are
infiltrated
by
during
response.
Given
innate
immune
mechanisms,
mainly
mediated
epithelial-derived
cytokines
(interleukin
[IL]-33,
IL-25,
TSLP
[thymic
stromal
lymphopoietin]),
induce
eosinophil-maturing/attractive
substances,
we
thought
to
evaluate
crosstalk
between
in
context
IL-33–mediated
inflammation.
DUOX1
was
previously
described
clinically
relevant
aspects
inflammation
a
HDM
-induced
asthma
mice
model,
patients
with
chronic
sinusitis
or
Thus,
evaluated
involvement
regulation
cells.
To
recapitulate
lung
environment
present
at
allergen
challenge
time
acute
asthma,
set
up
an
vitro
model
based
murine
bone
marrow–derived
differentiated
IL-5
then
activated
IL-33
(EOs33)
TC1
C57
We
found
induced
eosinophil-attractive
increased
expression.
Importantly,
coculture
EOs33
conditioned
medium
from
enhanced
expression
DUOX1,
which
further
combined
stimulation
(HDM
plus
EOs33).
Our
results
suggest
recruited
once
could
be
involved
loop
DUOX1-mediated
secretion.
Language: Английский