Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(20)
Published: May 11, 2023
Abstract
Isocitrate
dehydrogenase
(IDH)
mutation,
a
known
pathologic
classifier,
initiates
metabolic
reprogramming
in
glioma
cells
and
has
been
linked
to
the
reaction
status
of
glioma‐associated
microglia/macrophages
(GAMs).
However,
it
remains
unclear
how
IDH
genotypes
contribute
GAM
phenotypes.
Here,
is
demonstrated
that
gliomas
expressing
mutant
determine
M1‐like
polarization
GAMs,
while
archetypal
induces
M2‐like
polarization.
Intriguingly,
IDH‐mutant
secrete
excess
cholesterol,
resulting
cholesterol‐rich,
pro‐inflammatory
GAMs
without
altering
their
cholesterol
biosynthesis,
simultaneously
exhibiting
low
levels
tumoral
due
expression
remodeling
transport
molecules,
particularly
upregulation
ABCA1
downregulation
LDLR.
Mechanistically,
miR‐19a/LDLR
axis‐mediated
novel
post‐transcriptional
regulation
uptake
identified,
modulated
by
influencing
tumor
cell
proliferation
invasion.
mutation‐induced
PERK
activation
enhances
export
from
via
axis
ABCA1/APOE
upregulation.
Further,
synthetic
activator,
CCT020312
introduced,
which
markedly
stimulates
efflux
wild‐type
cells,
consequently
suppresses
The
findings
reveal
an
essential
role
PERK/miR‐19a/LDLR
signaling
pathway
orchestrating
gliomal
subsequent
phenotypes
thereby
highlighting
potential
target
for
therapy.
FEBS Journal,
Journal Year:
2022,
Volume and Issue:
290(6), P. 1420 - 1453
Published: Jan. 8, 2022
Alzheimer’s
disease
(AD)
is
an
age‐associated
neurodegenerative
disorder
with
multifactorial
etiology,
intersecting
genetic
and
environmental
risk
factors,
a
lack
of
disease‐modifying
therapeutics.
While
the
abnormal
accumulation
lipids
was
described
in
very
first
report
AD
neuropathology,
it
not
until
recent
decades
that
lipid
dyshomeostasis
became
focus
research.
Clinically,
lipidomic
metabolomic
studies
have
consistently
shown
alterations
levels
various
classes
emerging
early
stages
brains.
Mechanistically,
discovery
research
revealed
multifaceted
interactions
between
metabolism
key
pathogenic
mechanisms
including
amyloidogenesis,
bioenergetic
deficit,
oxidative
stress,
neuroinflammation,
myelin
degeneration.
In
present
review,
converging
evidence
defining
summarized,
followed
by
discussions
on
which
contributes
to
pathogenesis
modifies
risk.
Furthermore,
lipid‐targeting
therapeutic
strategies,
modification
their
efficacy
stage,
ApoE
status,
metabolic
vascular
profiles,
are
reviewed.
Science Advances,
Journal Year:
2022,
Volume and Issue:
8(37)
Published: Sept. 16, 2022
Lipids
are
crucial
components
of
cellular
function
owing
to
their
role
in
membrane
formation,
intercellular
signaling,
energy
storage,
and
homeostasis
maintenance.
In
the
brain,
lipid
dysregulations
have
been
associated
with
etiology
progression
neurodegeneration
other
neurological
pathologies.
Hence,
brain
lipids
emerging
as
important
potential
targets
for
early
diagnosis
prognosis
diseases.
This
review
aims
highlight
significance
usefulness
lipidomics
diagnosing
treating
We
explored
alterations
diseases,
paying
attention
organ-specific
characteristics
functions
lipids.
As
recent
advances
would
impossible
without
analytical
techniques,
we
provide
up-to-date
information
on
mass
spectrometric
approaches
integrative
analysis
omic
approaches.
Last,
present
applications
combined
artificial
intelligence
techniques
interdisciplinary
collaborative
research
diseases
clinical
heterogeneities.
Frontiers in Molecular Neuroscience,
Journal Year:
2022,
Volume and Issue:
15
Published: Aug. 25, 2022
Alzheimer’s
disease
(AD)
is
a
neurodegenerative
disorder
that
one
of
the
most
devastating
and
widespread
diseases
worldwide,
mainly
affecting
aging
population.
One
key
factors
contributing
to
AD-related
neurotoxicity
production
aggregation
amyloid
β
(Aβ).
Many
studies
have
shown
ability
Aβ
bind
cell
membrane
disrupt
its
structure,
leading
death.
Because
damage
affects
different
parts
brain
differently,
it
seems
likely
not
only
but
also
nature
interface
with
which
interacts,
helps
determine
final
neurotoxic
effect.
cholesterol
dominant
component
plasma
membrane,
plays
an
important
role
in
Aβ-induced
toxicity.
Elevated
levels
their
regulation
by
statins
been
be
influencing
progression
neurodegeneration.
However,
data
from
many
has
both
neuroprotective
aggravating
effects
relation
development
AD.
In
this
review,
we
attempt
summarize
recent
findings
on
toxicity
mediated
binding
pathogenesis
AD
consider
broader
context
lipid
composition
membranes.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
158, P. 114206 - 114206
Published: Jan. 5, 2023
The
term
type
III
diabetes
(T3DM)
has
been
proposed
for
Alzheimer's
disease
(AD)
due
to
the
shared
molecular
and
cellular
features
between
2
(T2DM)
insulin
resistance-associated
memory
deficits
cognitive
decline
in
elderly
individuals.
Astrocytes
elicit
neuroprotective
or
deleterious
effects
AD
progression
severity.
Patients
with
T2DM
are
at
a
high
risk
of
impairment,
targeting
astrocytes
might
be
promising
alleviating
neurodegeneration
diabetic
brain.
Recent
studies
focusing
on
cell-specific
activities
brain
have
revealed
important
role
metabolism
(e.g.,
glucose
metabolism,
lipid
metabolism),
neurovascular
coupling,
synapses,
synaptic
plasticity.
In
this
review,
we
discuss
how
their
dysfunction
result
multiple
pathological
clinical
from
metabolic
perspective
potential
comorbid
mechanism
these
two
diseases
astrocytes.
Annual Review of Neuroscience,
Journal Year:
2023,
Volume and Issue:
46(1), P. 59 - 78
Published: July 10, 2023
All
mammalian
cell
membranes
contain
cholesterol
to
maintain
membrane
integrity.
The
transport
of
this
hydrophobic
lipid
is
mediated
by
lipoproteins.
Cholesterol
especially
enriched
in
the
brain,
particularly
synaptic
and
myelin
membranes.
Aging
involves
changes
sterol
metabolism
peripheral
organs
also
brain.
Some
those
alterations
have
potential
promote
or
counteract
development
neurodegenerative
diseases
during
aging.
Here,
we
summarize
current
knowledge
general
principles
humans
mice,
most
widely
used
model
organism
biomedical
research.
We
discuss
that
occur
aged
brain
highlight
recent
developments
type-specific
fast-growing
research
field
aging
age-related
diseases,
focusing
on
Alzheimer's
disease.
propose
handling
interplay
between
types
critically
influence
disease
processes.
The Journal of Experimental Medicine,
Journal Year:
2024,
Volume and Issue:
221(4)
Published: March 1, 2024
Alzheimer’s
disease
(AD)
is
characterized
by
amyloid
plaques
and
neurofibrillary
tangles,
in
addition
to
neuroinflammation
changes
brain
lipid
metabolism.
25-Hydroxycholesterol
(25-HC),
a
known
modulator
of
both
inflammation
metabolism,
produced
cholesterol
25-hydroxylase
encoded
Ch25h
expressed
as
“disease-associated
microglia”
signature
gene.
However,
whether
influences
tau-mediated
neurodegeneration
unknown.
Here,
we
show
that
the
absence
resultant
reduction
25-HC,
there
strikingly
reduced
age-dependent
hippocampus
entorhinal/piriform
cortex
PS19
mice,
which
express
P301S
mutant
human
tau
transgene.
Transcriptomic
analyses
bulk
hippocampal
tissue
single
nuclei
revealed
deficiency
mice
strongly
suppressed
proinflammatory
signaling
microglia.
Our
results
suggest
key
role
for
Ch25h/25-HC
potentiating
promote
neurodegeneration.
may
represent
novel
therapeutic
target
primary
tauopathies,
AD,
other
neuroinflammatory
diseases.
Experimental & Molecular Medicine,
Journal Year:
2024,
Volume and Issue:
56(8), P. 1685 - 1690
Published: Aug. 1, 2024
The
brain
contains
the
highest
concentration
of
cholesterol
in
human
body,
which
emphasizes
importance
physiology.
Cholesterol
is
involved
neurogenesis
and
synaptogenesis,
age-related
reductions
levels
can
lead
to
synaptic
loss
impaired
plasticity,
potentially
contribute
neurodegeneration.
maintenance
homeostasis
neuronal
plasma
membrane
essential
for
normal
function,
imbalances
distribution
are
associated
with
various
neurodegenerative
disorders,
including
Alzheimer's
disease,
Parkinson's
Huntington's
disease.
This
review
aims
explore
molecular
pathological
mechanisms
by
imbalance
neurotransmission
defects
neurodegeneration,
focusing
on
four
key
mechanisms:
(1)
dysfunction,
(2)
alterations
structure
protein
clustering,
(3)
oligomers
amyloid
beta
(Aβ)
protein,
(4)
α-synuclein
aggregation.
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(1), P. 10 - 10
Published: Jan. 2, 2025
Huntington's
disease
(HD)
is
a
multifaceted
neurological
disorder
characterized
by
the
progressive
deterioration
of
motor,
cognitive,
and
psychiatric
functions.
Despite
limited
understanding
its
pathogenesis,
research
has
implicated
abnormal
trinucleotide
cytosine-adenine-guanine
CAG
repeat
expansion
in
huntingtin
gene
(HTT)
as
critical
factor.
The
development
innovative
strategies
imperative
for
early
detection
predictive
biomarkers,
enabling
timely
intervention
mitigating
irreversible
cellular
damage.
Lipidomics,
comprehensive
analytical
approach,
emerged
an
indispensable
tool
systematically
characterizing
lipid
profiles
elucidating
their
role
pathology.
A
MedLine
search
was
performed
to
identify
studies
that
use
lipidomics
characterization
HD.
Search
terms
included
"Huntington
disease";
"lipidomics";
"biomarker
discovery";
"NMR";
"Mass
spectrometry".
This
review
highlights
significance
HD
diagnosis
treatment,
exploring
changes
brain
lipids
Recent
breakthroughs
techniques,
particularly
mass
spectrometry
NMR
spectroscopy,
have
revolutionized
research,
researchers
gain
deeper
insights
into
complex
lipidome
brain.
broad
spectrum
alterations
vital
precise
diagnostic
evaluation
effective
management.
integration
with
artificial
intelligence
interdisciplinary
collaboration
holds
promise
addressing
clinical
variability