Frontiers in Cardiovascular Medicine,
Journal Year:
2020,
Volume and Issue:
7
Published: Nov. 17, 2020
Adipose
tissue
is
a
critical
regulator
of
systemic
metabolism
and
bodily
homeostasis
as
it
secretes
myriad
adipokines,
including
inflammatory
anti-inflammatory
cytokines.
As
the
main
storage
pool
lipids,
subcutaneous
visceral
adipose
tissues
undergo
marked
hypertrophy
hyperplasia
in
response
to
nutritional
excess
leading
hypoxia,
adipokine
dysregulation
subsequent
low-grade
inflammation
that
characterized
by
increased
infiltration
activation
innate
adaptive
immune
cells.
The
specific
localization,
physiology,
susceptibility
heterogeneity
cell
population
each
depot
are
unique
thus
dictate
possible
complications
chronic
inflammation.
Several
lines
evidence
link
particularly
perivascular,
pericardial
perirenal
development
metabolic
syndrome,
insulin
resistance,
type
2
diabetes
cardiovascular
diseases.
In
addition
implication
system
regulation
function,
components
pivotal
detrimental
or
otherwise
favorable
remodeling
thermogenesis.
resident
infiltrating
cells
morphological
adaptation
based
on
energy
status
better
comprehension
address
this
review,
we
discuss
role
across
various
physiological
pathophysiological
states
pertain
progression
diseases
associated
with
disorders.
Understanding
such
mechanisms
allows
for
exploitation
tissue-immune
crosstalk,
exploring
how
might
be
targeted
strategy
treat
derangements
dysfunctions.
Gut Microbes,
Journal Year:
2025,
Volume and Issue:
17(1)
Published: Feb. 20, 2025
Next-generation
live
biotherapeutics
are
promising
to
aid
the
treatment
of
obesity
and
metabolic
diseases.
Here,
we
reported
a
novel
anti-obesity
probiotic
candidate,
Roseburia
hominis,
that
was
depleted
in
stool
samples
obese
subjects
compared
with
lean
controls,
its
abundance
negatively
correlated
body
mass
index
serum
triglycerides.
Supplementation
R.
hominis
prevented
weight
gain
disorders
glucose
lipid
metabolism,
fatty
liver,
inhibited
white
adipose
tissue
expansion
brown
whitening
mice
fed
high-fat
diet,
boosted
lean-related
species.
The
effects
could
be
partially
attributed
production
nicotinamide
riboside
upregulation
Sirtuin1/mTOR
signaling
pathway.
These
results
indicated
is
candidate
for
development
next-generation
prevention
Biochemical Journal,
Journal Year:
2020,
Volume and Issue:
477(6), P. 1089 - 1107
Published: March 23, 2020
Adipose
tissue
regulates
metabolic
homeostasis
by
participating
in
endocrine
and
immune
responses
addition
to
storing
releasing
lipids
from
adipocytes.
Obesity
skews
adipose
adipokine
degrades
the
coordination
of
adipocyte
lipogenesis
lipolysis.
These
defects
metabolism
can
promote
ectopic
lipid
deposition
inflammation
insulin-sensitive
tissues
such
as
skeletal
muscle
liver.
Sustained
caloric
excess
expand
white
a
point
maladaptation
exacerbating
both
local
systemic
inflammation.
Multiple
sources,
instigators
propagators
occur
during
obesity.
Cross-talk
between
professional
cells
(i.e.
macrophages)
adipocytes)
stress
metaflammation).
Metabolic
endogenous
danger
signals
engage
pathogen
recognition
receptors
(PRRs)
innate
system
thereby
activating
pro-inflammatory
pathways
tissue.
The
Nod-like
receptor
protein
3
(NLRP3)
inflammasome
act
sensor
wide
range
pathogen-
damage-associated
molecular
patterns
(PAMPs
DAMPs).
Activation
NLRP3
facilitates
caspase-1
dependent
production
cytokines
IL-1β
IL-18.
pyroptotic
cell
death,
but
is
also
involved
adipogenesis.
This
review
discusses
role
immunometabolism
relevant
disease.
Understanding
potential
sources
activation
consequences
effectors
may
reveal
therapeutic
opportunities
break
or
fine-tune
connection
Metabolites,
Journal Year:
2020,
Volume and Issue:
10(5), P. 179 - 179
Published: April 30, 2020
White
adipose
tissue
(WAT)
is
a
highly
adaptive
endocrine
organ
that
continuously
remodels
in
response
to
nutritional
cues.
WAT
expands
store
excess
energy
by
increasing
adipocyte
number
and/or
size.
Failure
expansion
has
serious
consequences
on
metabolic
health
resulting
altered
lipid,
glucose,
and
inflammatory
profiles.
Besides
an
impaired
adipogenesis,
fibrosis
low-grade
inflammation
also
characterize
dysfunctional
WAT.
Nevertheless,
the
precise
mechanisms
leading
expansibility
are
yet
unresolved.
Autophagy
conserved
essential
process
for
cellular
homeostasis,
which
constitutively
allows
recycling
of
damaged
or
long-lived
proteins
organelles,
but
induced
under
stress
conditions
provide
nutrients
remove
pathogens.
By
modulating
protein
organelle
content,
autophagy
cell
remodeling,
maintenance,
survival.
In
this
line,
been
involved
many
processes
affected
during
maladaptation,
including
adipocyte,
macrophage
function,
response,
fibrosis.
dysregulation
related
obesity
diabetes.
However,
it
remains
unclear
whether
alteration
obese
diabetic
patients
cause
consequence
malfunction.
review,
current
data
regarding
these
issues
discussed,
focusing
evidence
from
human
studies.
Frontiers in Cardiovascular Medicine,
Journal Year:
2020,
Volume and Issue:
7
Published: Nov. 17, 2020
Adipose
tissue
is
a
critical
regulator
of
systemic
metabolism
and
bodily
homeostasis
as
it
secretes
myriad
adipokines,
including
inflammatory
anti-inflammatory
cytokines.
As
the
main
storage
pool
lipids,
subcutaneous
visceral
adipose
tissues
undergo
marked
hypertrophy
hyperplasia
in
response
to
nutritional
excess
leading
hypoxia,
adipokine
dysregulation
subsequent
low-grade
inflammation
that
characterized
by
increased
infiltration
activation
innate
adaptive
immune
cells.
The
specific
localization,
physiology,
susceptibility
heterogeneity
cell
population
each
depot
are
unique
thus
dictate
possible
complications
chronic
inflammation.
Several
lines
evidence
link
particularly
perivascular,
pericardial
perirenal
development
metabolic
syndrome,
insulin
resistance,
type
2
diabetes
cardiovascular
diseases.
In
addition
implication
system
regulation
function,
components
pivotal
detrimental
or
otherwise
favorable
remodeling
thermogenesis.
resident
infiltrating
cells
morphological
adaptation
based
on
energy
status
better
comprehension
address
this
review,
we
discuss
role
across
various
physiological
pathophysiological
states
pertain
progression
diseases
associated
with
disorders.
Understanding
such
mechanisms
allows
for
exploitation
tissue-immune
crosstalk,
exploring
how
might
be
targeted
strategy
treat
derangements
dysfunctions.