International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(14), P. 7634 - 7634
Published: July 17, 2021
Exacerbations
largely
determine
the
character
of
progression
and
prognosis
chronic
obstructive
pulmonary
disease
(COPD).
are
connected
with
changes
in
microbiological
landscape
bronchi
due
to
a
violation
their
immune
homeostasis.
Many
metabolic
processes
involved
COPD
associated
bacterial
colonization
bronchi.
The
objective
this
review
is
analysis
molecular
mechanisms
lipid
metabolism
response
disorders
lungs
exacerbations.
complex
role
pathogenesis
some
infections
only
beginning
be
understood,
however,
there
already
fewer
doubts
even
now
about
its
significance
both
infectious
exacerbations
general
disease.
It
shown
that
rafts
plasma
membranes
cells
many
related
detection
pathogens,
signal
transduction,
penetration
pathogens
into
cell.
Smoking
disrupts
normally
proceeded
lungs,
which
part
pathogenesis.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(7), P. 3790 - 3790
Published: March 28, 2024
Cutaneous
wound
healing
is
a
complex
biological
process
involving
series
of
well-coordinated
events
aimed
at
restoring
skin
integrity
and
function.
Various
experimental
models
have
been
developed
to
study
the
mechanisms
underlying
repair
evaluate
potential
therapeutic
interventions.
This
review
explores
diverse
array
utilized
in
research,
ranging
from
rodent
excisional
wounds
advanced
tissue
engineering
constructs
microfluidic
platforms.
More
importantly,
influence
lipids
on
examined,
emphasizing
their
role
enhancing
barrier
function
restoration,
modulating
inflammation,
promoting
cell
proliferation,
remodeling.
Lipids,
such
as
phospholipids,
sphingolipids,
ceramides,
play
crucial
roles
membrane
structure,
signaling,
repair.
Understanding
interplay
between
microenvironment
provides
valuable
insights
into
development
novel
strategies
for
efficient
regeneration.
highlights
significance
investigating
elucidating
intricate
involvement
process,
offering
avenues
improving
clinical
outcomes
management.
Frontiers in Microbiology,
Journal Year:
2021,
Volume and Issue:
12
Published: Feb. 4, 2021
Membrane
rafts
are
dynamic,
small
(10–200
nm)
domains
enriched
with
cholesterol
and
sphingolipids
that
compartmentalize
cellular
processes.
Rafts
participate
in
roles
essential
to
the
lifecycle
of
different
viral
families
including
virus
entry,
assembly
and/or
budding
events.
seem
attachment
recruitment
cell
surface,
as
well
endocytic
non-endocytic
mechanisms
some
viruses
use
enter
host
cells.
In
this
review,
we
will
introduce
specific
role
entry
define
factors
implied
choice
one
pathway
over
others.
Finally,
summarize
most
relevant
information
about
raft
participation
process
enveloped
non-enveloped
viruses.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: Dec. 16, 2021
Since
its
appearance,
the
Severe
Acute
Respiratory
Syndrome
Coronavirus
(SARS-CoV-2),
causal
agent
of
Disease
2019
(COVID-19),
represents
a
global
problem
for
human
health
that
involves
host
lipid
homeostasis.
Regarding,
rafts
are
functional
membrane
microdomains
with
highly
and
tightly
packed
molecules.
These
regions
enriched
in
sphingolipids
cholesterol
recruit
concentrate
several
receptors
molecules
involved
pathogen
recognition
cellular
signaling.
Cholesterol-rich
have
multiple
functions
viral
replication;
however,
their
role
SARS-CoV-2
infection
remains
unclear.
In
this
review,
we
discussed
novel
evidence
on
cholesterol-rich
as
platform
entry,
where
such
angiotensin-converting
enzyme-2
(ACE-2),
heparan
sulfate
proteoglycans
(HSPGs),
Toll-like
(TLRs),
transmembrane
serine
proteases
(TMPRSS),
CD-147
HDL-scavenger
receptor
B
type
1
(SR-B1)
recruited
interaction
spike
protein.
FDA-approved
drugs
statins,
metformin,
hydroxychloroquine,
cyclodextrins
(methyl-β-cyclodextrin)
can
disrupt
to
regulate
key
immune
signaling
pathways
triggered
by
infection.
Taken
together,
better
knowledge
SARS-CoV-2-host
interactions
will
provide
valuable
insights
into
pathogenesis
identification
therapeutic
targets.
International Journal of Molecular Sciences,
Journal Year:
2020,
Volume and Issue:
21(23), P. 8992 - 8992
Published: Nov. 26, 2020
Carbohydrates,
fats,
and
proteins
are
the
underlying
energy
sources
for
animals
catabolized
through
specific
biochemical
cascades
involving
numerous
enzymes.
The
catabolites
metabolites
in
these
metabolic
pathways
crucial
many
cellular
functions;
therefore,
an
imbalance
and/or
dysregulation
of
causes
dysfunction,
resulting
various
diseases.
Bone,
a
highly
mineralized
organ
that
serves
as
skeleton
body,
undergoes
continuous
active
turnover,
which
is
required
maintenance
healthy
bony
components
deposition
resorption
bone
matrix
minerals.
This
coordinated
event
regulated
throughout
life
by
cells
such
osteoblasts,
osteoclasts,
osteocytes,
requires
synchronized
activities
from
different
pathways.
Here,
we
aim
to
provide
comprehensive
review
metabolism
involved
development
homeostasis,
revealed
mouse
genetic
studies.
Cellular and Molecular Immunology,
Journal Year:
2022,
Volume and Issue:
19(3), P. 327 - 336
Published: Jan. 11, 2022
Cholesterol
is
a
critical
lipid
for
all
mammalian
cells,
ensuring
proper
membrane
integrity,
fluidity,
and
biochemical
function.
Accumulating
evidence
indicates
that
macrophages
rapidly
profoundly
reprogram
their
cholesterol
metabolism
in
response
to
activation
signals
support
host
defense
processes.
However,
our
understanding
of
the
molecular
details
underlying
how
why
homeostasis
specifically
reshaped
during
immune
responses
remains
less
well
understood.
This
review
discusses
current
knowledge
cellular
homeostatic
machinery
introduces
emerging
concepts
regarding
plasma
partitioned
into
distinct
pools.
We
then
discuss
proinflammatory
can
markedly
reshape
macrophages,
with
focus
on
differences
between
MyD88-dependent
pattern
recognition
receptors
interferon
signaling
pathway.
also
recent
work
investigating
capacity
these
selectively
homeostasis.
examine
changes
influence
sensitivity
set
microbial
pore-forming
toxins
known
as
cholesterol-dependent
cytolysins
target
effector
functions.
whether
metabolic
reprogramming
be
leveraged
therapy
mitigate
tissue
damage
mediated
by
necrotizing
fasciitis
other
related
infections.
expect
advancing
crosstalk
innate
immunity
will
help
explain
inflammation
underlies
diseases
highlight
pathways
could
targeted
normalize
disease
states.
Nutrients,
Journal Year:
2022,
Volume and Issue:
14(16), P. 3417 - 3417
Published: Aug. 19, 2022
Lipid
rafts
in
cell
plasma
membranes
play
a
critical
role
the
life
cycle
of
many
viruses.
However,
involvement
membrane
cholesterol-rich
lipid
entry
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
into
target
cells
is
not
well
known.
In
this
study,
we
investigated
whether
presence
microdomains
required
for
SARS-CoV-2
host
cells.
Our
results
show
that
depletion
cholesterol
by
methyl-beta-cyclodextrin
(MβCD)
treatment
impaired
expression
surface
receptor
angiotensin-converting
enzyme
(ACE2),
resulting
significant
increase
The
effects
exerted
MβCD
could
be
substantially
reversed
exogenous
replenishment.
contrast,
disturbance
intracellular
homeostasis
statins
or
siRNA
knockdown
key
genes
involved
biosynthesis
and
transport
pathways
reduced
study
also
reveals
SREBP2-mediated
process
These
suggest
cholesterol-enriched
cellular
are
essential
Pharmacological
manipulation
might
provide
new
therapeutic
strategies
to
alleviate
Circulation Research,
Journal Year:
2024,
Volume and Issue:
134(7)
Published: Feb. 20, 2024
BACKGROUND:
Many
cardiovascular
pathologies
are
induced
by
signaling
through
G-protein-coupled
receptors
via
Gsα
(G
protein
stimulatory
α
subunit)
proteins.
However,
the
specific
cellular
mechanisms
that
driven
and
contribute
to
development
of
atherosclerosis
remain
unclear.
METHODS:
High-throughput
screening
involving
data
from
single-cell
bulk
sequencing
were
used
explore
expression
in
atherosclerosis.
The
differentially
activity
analyzed
immunofluorescence
cAMP
measurements.
Macrophage-specific
knockout
(Mac-Gsα
KO
)
mice
generated
study
effect
on
role
was
determined
transplanting
bone
marrow
performing
assays
for
foam
cell
formation,
Dil-ox-LDL
(oxidized
low-density
lipoprotein)
uptake,
chromatin
immunoprecipitation,
luciferase
reporter
assays.
RESULTS:
ScRNA-seq
showed
elevated
Gnas
atherosclerotic
mouse
aorta’s
cholesterol
metabolism
macrophage
cluster,
while
confirmed
increased
GNAS
human
plaque
content.
A
significant
upregulation
active
occurred
macrophages
plaques.
Ox-LDL
could
translocate
lipid
rafts
short-term
promote
transcription
ERK1/2
activation
C/EBPβ
phosphorylation
oxidative
stress
long-term.
Atherosclerotic
lesions
Mac-Gsα
displayed
decreased
deposition
compared
with
those
control
mice.
Additionally,
deficiency
alleviated
uptake
formation.
Mechanistically,
levels
transcriptional
response
element
binding
protein,
which
resulted
CD36
SR-A1.
In
translational
experiments,
inhibiting
suramin
or
cpGN13
reduced
progression
plaques
vivo.
CONCLUSIONS:
is
enhanced
during
increases
genetic
chemical
inactivation
inhibit
mice,
suggesting
drugs
targeting
may
be
useful
treatment
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: July 4, 2024
T
lymphocytes
play
a
primary
role
in
the
adaptive
antiviral
immunity.
Both
lymphocytosis
and
lymphopenia
were
found
to
be
associated
with
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
While
indicates
an
active
anti-viral
response,
is
sign
of
poor
prognosis.
T-cells,
essence,
rarely
express
ACE2
receptors,
making
cause
cell
depletion
enigmatic.
Moreover,
emerging
strains
posed
immunological
challenge,
potentially
alarming
for
next
pandemic.
Herein,
we
review
how
possible
indirect
direct
key
mechanisms
could
contribute
SARS-CoV-2-associated-lymphopenia.
The
fundamental
mechanism
inflammatory
cytokine
storm
elicited
by
viral
infection,
which
alters
host
metabolism
into
more
acidic
state.
This
"hyperlactic
acidemia"
together
suppresses
T-cell
proliferation
triggers
intrinsic/extrinsic
apoptosis.
SARS-CoV-2
infection
also
results
shift
from
steady-state
hematopoiesis
stress
hematopoiesis.
Even
low
expression,
presence
cholesterol-rich
lipid
rafts
on
activated
T-cells
may
enhance
entry
syncytia
formation.
Finally,
indicate
participation
other
receptors
or
auxiliary
proteins
that
can
work
alone
concert
mechanisms.
Therefore,
address
CD147-a
novel
route-for
its
new
variants.
CD147
not
only
expressed
but
it
interacts
co-partners
orchestrate
various
biological
processes.
Given
these
features,
appealing
candidate
pathogenicity.
Understanding
molecular
cellular
behind
SARS-CoV-2-associated-lymphopenia
will
aid
discovery
potential
therapeutic
targets
improve
resilience
our
immune
system
against
this
rapidly
evolving
virus.