Macrophage polarization and its impact on idiopathic pulmonary fibrosis
Zhouling Ge,
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Yong Q. Chen,
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Leikai Ma
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et al.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: July 26, 2024
Idiopathic
pulmonary
fibrosis
(IPF)
is
a
lung
disease
that
worsens
over
time,
causing
in
the
lungs
and
ultimately
resulting
respiratory
failure
high
risk
of
death.
Macrophages
play
crucial
role
immune
system,
showing
flexibility
by
transforming
into
either
pro-inflammatory
(M1)
or
anti-inflammatory
(M2)
macrophages
when
exposed
to
different
stimuli,
impacting
development
IPF.
Recent
research
has
indicated
polarization
onset
progression
M1
secrete
inflammatory
cytokines
agents
early
damage
fibrosis,
while
M2
support
tissue
healing
releasing
cytokines.
Developing
novel
treatments
for
IPF
relies
on
thorough
comprehension
processes
involved
macrophage
The
review
outlines
regulation
its
impact
IPF,
with
goal
investigating
possible
therapeutic
benefits
advancement
Language: Английский
Multi-omics and chemical profiling approaches to understand the material foundation and pharmacological mechanism of sophorae tonkinensis radix et rhizome-induced liver injury in mice
Si-wei Rao,
No information about this author
Chengjun Liu,
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Dong Liang
No information about this author
et al.
Journal of Ethnopharmacology,
Journal Year:
2024,
Volume and Issue:
330, P. 118224 - 118224
Published: April 19, 2024
Language: Английский
Role of pattern recognition receptors in the development of MASLD and potential therapeutic applications
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
175, P. 116724 - 116724
Published: May 17, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
has
become
one
of
the
most
prevalent
diseases
worldwide,
and
its
occurrence
is
strongly
associated
with
obesity,
insulin
resistance
(IR),
genetics,
metabolic
stress.
Ranging
from
simple
fatty
to
steatohepatitis
(MASH),
even
severe
complications
such
as
fibrosis
advanced
cirrhosis
or
hepatocellular
carcinoma,
underlying
mechanisms
MASLD
progression
are
complex
involve
multiple
cellular
mediators
related
signaling
pathways.
Pattern
recognition
receptors
(PRRs)
innate
immune
system,
including
Toll-like
(TLRs),
C-type
lectin
(CLRs),
NOD-like
(NLRs),
RIG-like
(RLRs),
DNA
receptors,
have
been
demonstrated
potentially
contribute
pathogenesis
for
MASLD.
Their
pathways
can
induce
inflammation,
mediate
oxidative
stress,
affect
gut
microbiota
balance,
ultimately
resulting
in
hepatic
steatosis,
inflammatory
injury
fibrosis.
Here
we
review
available
literature
regarding
involvement
PRR-associated
signals
pathogenic
clinical
features
MASLD,
vitro
animal
models
We
also
discuss
emerging
targets
PRRs
drug
developments
that
involved
agent
therapies
intended
arrest
reverse
progression,
thus
enabling
refinement
therapeutic
accelerate
development.
Language: Английский
Exercise promotes peripheral glycolysis in skeletal muscle through miR-204 induction via the HIF-1α pathway
Sang R. Lee,
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Kang Joo Jeong,
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Moeka Mukae
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et al.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 9, 2025
The
mechanisms
underlying
exercise-induced
insulin
sensitization
are
of
great
interest,
as
exercise
is
a
clinically
critical
intervention
for
diabetic
patients.
Some
microRNAs
(miRs)
secreted
from
skeletal
muscle
after
where
they
regulate
sensitivity,
and
have
potential
diagnostic
markers
in
miR-204
well-known
its
involvement
development,
cancer,
metabolism;
however,
role
glycemic
control
remains
unclear.
In
the
present
study,
endurance
mice
increased
expression
levels
muscle.
chronic
model,
were
elevated
along
with
glycolytic
enzymes
When
muscular
hypoxia
was
induced
exercise,
also
upregulation
hypoxia-inducible
factor
1-alpha
(HIF-1α).
Furthermore,
HIF-1α
overexpression
led
to
expression.
Treatment
mimic
C2C12
cells
significantly
enhanced
glycolysis
rate
mRNA
enzymes.
Notably,
intravenous
administration
glucose
clearance
following
refeeding.
initially
blood
at
an
early
stage
refeeding
but
later
promoted
reduction
continued.
Additionally,
upregulated
muscles
miR-204-injected
mice.
These
findings
suggest
novel
physiological
promoting
glycolysis,
particularly
situations
action
limited.
Language: Английский
Advancing precision medicine in metabolic dysfunction-associated steatotic liver disease
Trends in Endocrinology and Metabolism,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
Language: Английский
E2F2 Reprograms Macrophage Function By Modulating Material and Energy Metabolism in the Progression of Metabolic Dysfunction‐Associated Steatohepatitis
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(48)
Published: Oct. 28, 2024
Abstract
Macrophages
are
essential
for
the
development
of
steatosis,
hepatic
inflammation,
and
fibrosis
in
metabolic
dysfunction‐associated
steatohepatitis(MASH).
However,
roles
macrophage
E2F2
progression
MASH
have
not
been
elucidated.
This
study
reveals
that
expression
is
dramatically
downregulated
livers
from
mice
humans,
this
adversely
correlated
with
severity
disease.
Myeloid‐specific
depletion
aggravates
intrahepatic
stellate
cell
activation,
hepatocyte
lipid
accumulation
during
progression.
Mechanistically,
can
inhibit
SLC7A5
transcription
directly.
deficiency
upregulates
to
mediate
amino
acids
flux,
resulting
enhanced
glycolysis,
impaired
mitochondrial
function,
increased
macrophages
proinflammatory
response
a
Leu‐mTORC1‐dependent
manner.
Moreover,
bioinformatics
analysis
CUT
&Tag
assay
identify
direct
binding
Nrf2
promoter
promote
its
nuclear
translocation.
Genetic
or
pharmacological
activation
effectively
activates
attenuate
Finally,
patients
treated
CDK4/6
inhibitors
demonstrate
reduced
activity
but
PBMCs.
These
findings
indicated
suppresses
by
reprogramming
acid
metabolism
via
SLC7A5‐
Leu‐mTORC1
signaling
pathway.
Activating
holds
promise
as
therapeutic
strategy
MASH.
Language: Английский
Processed Buthus martensii Karsch scorpions ameliorate diet-induced NASH in mice by attenuating Kv1.3-mediated macrophage activation
Erjin Xu,
No information about this author
Ming Sang,
No information about this author
W. Xu
No information about this author
et al.
Journal of Ethnopharmacology,
Journal Year:
2024,
Volume and Issue:
337, P. 118794 - 118794
Published: Sept. 6, 2024
Language: Английский
Lipotoxicity-driven metabolic dysfunction-associated steatotic liver disease (MASLD)
Santiago Iturbe-Rey,
No information about this author
Cláudia Maccali,
No information about this author
Marco Arrese
No information about this author
et al.
Atherosclerosis,
Journal Year:
2024,
Volume and Issue:
400, P. 119053 - 119053
Published: Nov. 14, 2024
Metabolic
dysfunction-associated
steatotic
liver
disease
(MASLD)
encompasses
a
spectrum
of
lesions,
ranging
from
simple
steatosis
to
metabolic
steatohepatitis
(MASH),
that
may
further
progress
cirrhosis.
MASLD
is
estimated
affect
more
than
one
third
the
general
population
and
it
represents
risk
factor
for
end-stage
failure
cancer,
substantially
contributing
liver-related
morbidity
mortality.
Although
pathogenesis
incompletely
understood,
known
consist
multifactorial
process
influenced
by
extrinsic
intrinsic
factors
such
as
metabolic,
environmental
demographic
features,
gut
microbiota
genetics.
Dysregulation
both
extracellular
intracellular
lipid
composition
promote
generation
toxic
species,
thereby
triggering
lipotoxicity
cellular
stress.
These
events
ultimately
lead
activation
distinct
cell
death
pathways,
resulting
in
inflammation,
fibrogenesis
and,
eventually,
carcinogenesis.
In
this
manuscript,
we
provide
comprehensive
review
role
during
pathogenesis,
discussing
most
relevant
species
related
molecular
mechanisms,
summarizing
type-specific
effects
highlighting
promising
putative
therapeutic
strategies
modulating
metabolism
MASLD.
Language: Английский
Whole-Transcriptome Analysis Reveals Potential CeRNA Regulatory Mechanism in Takifugu rubripes against Cryptocaryon irritans Infection
Biology,
Journal Year:
2024,
Volume and Issue:
13(10), P. 788 - 788
Published: Oct. 1, 2024
Cryptocaryon
irritans
(C.
irritans)
is
a
proto-ciliate
parasite
that
infects
marine
fishes,
including
the
cultured
species
Takifugu
rubripes
(T.
rubripes),
causing
disease
and
potential
mortality.
In
host
organisms,
infection
by
parasites
triggers
an
immune
response
modulated
regulatory
elements
proteins
non-coding
RNAs.
this
study,
whole
transcriptome
RNA
sequencing
of
T.
gill
tissue
before
after
with
C.
was
performed
to
reveal
competitive
endogenous
(ceRNA)
network.
Histomorphology
revealed
segment
swelling
parasitic
invasion
in
infected
group.
The
analysis
identified
18
differentially
expressed
miRNAs
(DEMs),
214
lncRNAs
(DELs),
2501
genes
(DEGs),
7
circRNAs
(DECs)
Gene
Ontology
(GO)
enrichment
these
were
notably
enriched
Wnt
signaling
pathway
mTOR
pathway.
co-expression
networks
(lncRNA/circRNA-miRNA-mRNA)
constructed
based
on
correlation
Further
suggested
LOC105418663-circ_0000361-fru-miR-204a-fzd3a
ceRNA
axis
potentially
involved
regulation
responses
against
infection.
Finally,
expression
levels
DEG,
DEL,
DEM
validated.
This
study
reveals
mechanism
candidate
network,
providing
insights
into
rubripes’
irritans.
Language: Английский