Frontiers in Aging Neuroscience,
Journal Year:
2023,
Volume and Issue:
15
Published: Dec. 19, 2023
Copper
(Cu)
plays
a
crucial
role
as
trace
element
in
various
physiological
processes
humans.
Nonetheless,
free
copper
ions
accumulate
the
brain
over
time,
resulting
range
of
pathological
changes.
Compelling
evidence
indicates
that
excessive
deposition
contributes
to
cognitive
decline
individuals
with
Alzheimer’s
disease
(AD).
Free
levels
serum
and
AD
patients
are
notably
elevated,
leading
reduced
antioxidant
defenses
mitochondrial
dysfunction.
Moreover,
accumulation
triggers
specific
form
cell
death,
namely
copper-dependent
death
(cuproptosis).
This
article
aimed
review
correlation
between
dysregulation
pathogenesis
AD,
along
primary
pathways
regulating
homoeostasis
copper-induced
AD.
Additionally,
efficacy
safety
natural
synthetic
agents,
including
chelators,
lipid
peroxidation
inhibitors,
antioxidants,
were
examined.
These
treatments
can
restore
equilibrium
prevent
cases.
Another
aim
this
was
highlight
significance
promote
development
pharmaceutical
interventions
address
it.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Feb. 16, 2024
Abstract
The
human
gastrointestinal
tract
is
populated
with
a
diverse
microbial
community.
vast
genetic
and
metabolic
potential
of
the
gut
microbiome
underpins
its
ubiquity
in
nearly
every
aspect
biology,
including
health
maintenance,
development,
aging,
disease.
advent
new
sequencing
technologies
culture-independent
methods
has
allowed
researchers
to
move
beyond
correlative
studies
toward
mechanistic
explorations
shed
light
on
microbiome–host
interactions.
Evidence
unveiled
bidirectional
communication
between
central
nervous
system,
referred
as
“microbiota–gut–brain
axis”.
microbiota–gut–brain
axis
represents
an
important
regulator
glial
functions,
making
it
actionable
target
ameliorate
development
progression
neurodegenerative
diseases.
In
this
review,
we
discuss
mechanisms
As
provides
essential
cues
microglia,
astrocytes,
oligodendrocytes,
examine
communications
microbiota
these
cells
during
healthy
states
Subsequently,
diseases
using
metabolite-centric
approach,
while
also
examining
role
microbiota-related
neurotransmitters
hormones.
Next,
targeting
intestinal
barrier,
blood–brain
meninges,
peripheral
immune
system
counteract
dysfunction
neurodegeneration.
Finally,
conclude
by
assessing
pre-clinical
clinical
evidence
probiotics,
prebiotics,
fecal
transplantation
A
thorough
comprehension
will
foster
effective
therapeutic
interventions
for
management
Journal of Neuroinflammation,
Journal Year:
2023,
Volume and Issue:
20(1)
Published: Aug. 5, 2023
Microglia
are
the
resident
innate
immune
cells
in
brain
with
a
major
role
orchestrating
responses.
They
also
provide
frontline
of
host
defense
central
nervous
system
(CNS)
through
their
active
phagocytic
capability.
Being
professional
phagocyte,
microglia
participate
and
autophagic
clearance
cellular
waste
debris
as
well
toxic
protein
aggregates,
which
relies
on
optimal
lysosomal
acidification
function.
Defective
microglial
leads
to
impaired
functions
result
perpetuation
neuroinflammation
progression
neurodegeneration.
Reacidification
lysosomes
has
been
shown
reverse
neurodegenerative
pathology
Alzheimer's
disease.
In
this
review,
we
summarize
key
factors
mechanisms
contributing
impairment
associated
dysfunction
microglia,
how
these
defects
contribute
We
further
discuss
techniques
monitor
pH
therapeutic
agents
that
can
reacidify
under
disease
conditions.
Finally,
propose
future
directions
investigate
lysosome-mitochondria
crosstalk
neuron-glia
interaction
for
more
comprehensive
understanding
its
broader
CNS
physiological
pathological
implications.
Molecular Neurodegeneration,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: Jan. 16, 2024
Abstract
Protein
misfolding
and
accumulation
defines
a
prevailing
feature
of
many
neurodegenerative
disorders,
finally
resulting
in
the
formation
toxic
intra-
extracellular
aggregates.
Intracellular
aggregates
can
enter
space
be
subsequently
transferred
among
different
cell
types,
thus
spreading
between
connected
brain
districts.
Although
microglia
perform
predominant
role
removal
aggregated
proteins,
mounting
evidence
suggests
that
astrocytes
actively
contribute
to
clearing
process.
However,
molecular
mechanisms
used
by
remove
misfolded
proteins
are
still
largely
unknown.
Here
we
first
provide
brief
overview
progressive
transition
from
soluble
monomers
insoluble
fibrils
characterizes
amyloid
referring
α-Synuclein
Tau
as
archetypical
examples.
We
then
highlight
at
basis
astrocyte-mediated
clearance
with
focus
on
their
potential
ability
recognize,
collect,
internalize
digest
protein
Finally,
explore
targeting
future
therapeutic
approach
for
treatment
disorders
characterized
accumulation.
Frontiers in Cellular Neuroscience,
Journal Year:
2024,
Volume and Issue:
18
Published: Feb. 28, 2024
Traumatic
brain
injury
(TBI)
is
one
of
the
most
common
pathological
conditions
impacting
central
nervous
system
(CNS).
A
neurological
deficit
associated
with
TBI
results
from
a
complex
pathogenetic
mechanisms
including
glutamate
excitotoxicity,
inflammation,
demyelination,
programmed
cell
death,
or
development
edema.
The
critical
components
contributing
to
CNS
response,
damage
control,
and
regeneration
after
are
glial
cells–in
reaction
tissue
damage,
their
activation,
hypertrophy,
proliferation
occur,
followed
by
formation
scar.
scar
creates
barrier
in
damaged
helps
protect
acute
phase
post-injury.
However,
this
process
prevents
complete
recovery
late/chronic
producing
permanent
scarring,
which
significantly
impacts
function.
Various
types
participate
formation,
but
mostly
attributed
reactive
astrocytes
microglia,
play
important
roles
several
pathologies.
Novel
technologies
whole-genome
transcriptomic
epigenomic
analyses,
unbiased
proteomics,
show
that
both
microglia
represent
groups
heterogenic
subpopulations
different
genomic
functional
characteristics,
responsible
for
role
neurodegeneration,
neuroprotection
regeneration.
Depending
on
representation
distinct
glia
subpopulations,
as
well
regenerative
processes
delayed
neurodegeneration
may
thus
differ
nearby
remote
areas
structures.
This
review
summarizes
process,
where
resultant
effect
severity-,
region-
time-dependent
determined
model
distance
explored
area
lesion
site.
Here,
we
also
discuss
findings
concerning
intercellular
signaling,
long-term
possibilities
novel
therapeutical
approaches.
We
believe
comprehensive
study
an
emphasis
cells,
involved
post-injury
processes,
be
helpful
further
research
decisive
factor
when
choosing
model.
Glia,
Journal Year:
2022,
Volume and Issue:
71(4), P. 848 - 865
Published: Nov. 29, 2022
Microglial
cells
are
crucial
in
maintaining
central
nervous
system
(CNS)
homeostasis
and
mediating
CNS
disease
pathogenesis.
Increasing
evidence
supports
that
alterations
the
mechanical
properties
of
microenvironments
influence
glial
cell
phenotypes,
but
mechanisms
regulating
microglial
function
remain
elusive.
Here,
we
examined
mechanosensitive
Piezo1
channel
cells,
particularly,
how
activation
regulates
pro-inflammatory
production
cytokines,
using
BV2
primary
cells.
expression
was
detected
both
at
mRNA
protein
levels.
Application
activator
Yoda1
induced
Ca2+
flux
to
increase
intracellular
concentration
reduced
by
treatment
with
ruthenium
red,
a
inhibitor,
or
Piezo1-specific
siRNA,
supporting
functions
as
surface
-permeable
channel.
Priming
lipopolysaccharide
(LPS)
TNF-α
IL-6,
which
were
inhibited
Yoda1.
Furthermore,
LPS
priming
ERK,
p38
MAPKs,
NF-κB.
LPS-induced
NF-κB,
not
ERK
p38,
Yoda1-induced
inhibition
blunted
siRNA-mediated
depletion
and,
furthermore,
BAPTA-AM
prevent
increase.
Collectively,
our
results
support
downregulates
especially
initiating
signaling
inhibit
NF-κB
inflammatory
pathway.
These
findings
reveal
previously
unrecognized
mechanism
function,
raising
an
interesting
perspective
on
targeting
this
molecular
alleviate
neuroinflammation
associated
pathologies.
Neuron,
Journal Year:
2023,
Volume and Issue:
112(3), P. 342 - 361
Published: Nov. 14, 2023
Physical
forces
are
ubiquitous
in
biological
processes
across
scales
and
diverse
contexts.
This
review
highlights
the
significance
of
mechanical
nervous
system
development,
homeostasis,
disease.
We
provide
an
overview
signals
present
delve
into
mechanotransduction
mechanisms
translating
these
cues
biochemical
signals.
During
regulate
a
plethora
processes,
including
cell
proliferation,
differentiation,
migration,
network
formation,
cortex
folding.
Forces
then
continue
exerting
their
influence
on
physiological
such
as
neuronal
activity,
glial
function,
interplay
between
different
types.
Notably,
changes
tissue
mechanics
manifest
neurodegenerative
diseases
brain
tumors,
potentially
offering
new
diagnostic
therapeutic
target
opportunities.
Understanding
role
cellular
physiology
pathology
adds
facet
to
neurobiology,
shedding
light
many
that
remain
incompletely
understood.
Journal of Neuroinflammation,
Journal Year:
2023,
Volume and Issue:
20(1)
Published: Oct. 4, 2023
Abstract
Microglia
are
so
versatile
that
they
not
only
provide
immune
surveillance
for
central
nervous
system,
but
participate
in
neural
circuitry
development,
brain
blood
vessels
formation,
blood–brain
barrier
architecture,
and
intriguingly,
the
regulation
of
emotions
behaviors.
have
a
profound
impact
on
neuronal
survival,
wiring
synaptic
plasticity.
As
professional
phagocytic
cells
brain,
remove
dead
cell
debris
neurotoxic
agents
via
an
elaborate
mechanism.
The
functional
profile
microglia
varies
considerately
depending
age,
gender,
disease
context
other
internal
or
external
environmental
factors.
Numerous
studies
demonstrated
pivotal
involvement
neuropsychiatric
disorders,
including
negative
affection,
social
deficit,
compulsive
behavior,
fear
memory,
pain
symptoms
associated
with
major
depression
disorder,
anxiety
autism
spectrum
disorder
schizophrenia.
In
this
review,
we
summarized
latest
discoveries
regarding
microglial
ontogeny,
subtypes
state
spectrum,
biological
functions
mechanistic
underpinnings
emotional
behavioral
disorders.
Furthermore,
highlight
potential
microglia-targeted
therapies
propose
outstanding
questions
to
be
addressed
future
research
human
microglia.