ACS Chemical Neuroscience,
Journal Year:
2016,
Volume and Issue:
7(4), P. 470 - 483
Published: March 17, 2016
Neuroinflammation
is
implicated
in
the
pathophysiology
of
a
growing
number
human
disorders,
including
multiple
sclerosis,
chronic
pain,
traumatic
brain
injury,
and
amyotrophic
lateral
sclerosis.
As
result,
interest
development
novel
methods
to
investigate
neuroinflammatory
processes,
for
purpose
diagnosis,
new
therapies,
treatment
monitoring,
has
surged
over
past
15
years.
Neuroimaging
offers
wide
array
non-
or
minimally
invasive
techniques
characterize
processes.
The
intent
this
Review
provide
brief
descriptions
currently
available
neuroimaging
image
neuroinflammation
central
nervous
system
(CNS)
vivo.
Specifically,
because
relatively
widespread
accessibility
equipment
nuclear
imaging
(positron
emission
tomography
[PET];
single
photon
computed
[SPECT])
magnetic
resonance
(MRI),
we
will
focus
on
strategies
utilizing
these
technologies.
We
first
working
definition
"neuroinflammation"
then
discuss
study
that
target
(1)
activation
CNS
immunocompetent
cells
(e.g.
glial
with
TSPO
tracer
[11C]PBR28),
(2)
compromised
BBB
identification
MS
lesions
gadolinium-enhanced
MRI),
(3)
CNS-infiltration
circulating
immune
tracking
monocyte
infiltration
into
parenchyma
iron
oxide
nanoparticles
(4)
pathological
consequences
apoptosis
[99mTc]Annexin
V
accumulation
T2*
relaxometry).
This
provides
an
overview
state-of-the-art
which
have
potential
impact
patient
care
foreseeable
future.
Physiological Reviews,
Journal Year:
2017,
Volume and Issue:
98(1), P. 239 - 389
Published: Dec. 24, 2017
Astrocytes
are
neural
cells
of
ectodermal,
neuroepithelial
origin
that
provide
for
homeostasis
and
defense
the
central
nervous
system
(CNS).
highly
heterogeneous
in
morphological
appearance;
they
express
a
multitude
receptors,
channels,
membrane
transporters.
This
complement
underlies
their
remarkable
adaptive
plasticity
defines
functional
maintenance
CNS
development
aging.
tightly
integrated
into
networks
act
within
context
tissue;
astrocytes
control
at
all
levels
organization
from
molecular
to
whole
organ.
Progress in Retinal and Eye Research,
Journal Year:
2015,
Volume and Issue:
51, P. 1 - 40
Published: June 23, 2015
The
mammalian
retina
provides
an
excellent
opportunity
to
study
glia–neuron
interactions
and
the
of
glia
with
blood
vessels.
Three
main
types
glial
cells
are
found
in
that
serve
maintain
retinal
homeostasis:
astrocytes,
Müller
resident
microglia.
cells,
astrocytes
microglia
not
only
provide
structural
support
but
they
also
involved
metabolism,
phagocytosis
neuronal
debris,
release
certain
transmitters
trophic
factors
K+
uptake.
Astrocytes
mostly
located
nerve
fibre
layer
accompany
vessels
inner
nuclear
layer.
Indeed,
like
astrocytic
processes
cover
forming
barrier
fulfil
a
significant
role
ion
homeostasis.
Among
other
activities,
can
be
stimulated
macrophage
function,
as
well
interact
neurons
by
secreting
growth
factors.
This
review
summarizes
functional
relationships
between
neurons,
presenting
general
picture
recently
modified
based
on
experimental
observations.
preferential
involvement
distinct
terms
activity
is
discussed,
for
example,
while
may
progenitors
responsible
synaptic
pruning.
Since
different
participate
together
activities
retina,
it
imperative
explore
order
redundancy
heterogeneity
among
these
cells.
Recent
studies
revealed
association
cell
specific
functions.
Finally,
neuroprotective
effects
photoreceptors
ganglion
under
normal
adverse
conditions
will
explored.
Trends in Immunology,
Journal Year:
2020,
Volume and Issue:
41(9), P. 758 - 770
Published: Aug. 17, 2020
Astrocytes
are
neural
parenchymal
cells
that
ubiquitously
tile
the
central
nervous
system
(CNS).
In
addition
to
playing
essential
roles
in
healthy
tissue,
astrocytes
exhibit
an
evolutionarily
ancient
response
all
CNS
insults,
referred
as
astrocyte
reactivity.
Long
regarded
passive
and
homogeneous,
reactivity
is
being
revealed
a
heterogeneous
functionally
powerful
component
of
mammalian
innate
immunity.
Nevertheless,
concepts
about
what
comprises
it
does
incomplete
sometimes
controversial.
This
review
discusses
goal
differentiating
reactive
subtypes
states
based
on
composite
pictures
molecular
expression,
cell
morphology,
cellular
interactions,
proliferative
state,
normal
functions,
disease-induced
dysfunctions.
A
working
model
conceptual
framework
presented
for
characterizing
diversity
Frontiers in Cellular Neuroscience,
Journal Year:
2017,
Volume and Issue:
11
Published: Feb. 13, 2017
Glial
cells,
consisting
of
microglia,
astrocytes
and
oligodendrocyte
lineage
cells
as
their
major
components,
constitute
a
large
fraction
the
mammalian
brain.
Originally
considered
purely
non-functional
glue
for
neurons,
decades
research
have
highlighted
importance
well
further
functions
glial
cells.
Although
many
aspects
these
are
characterized
nowadays,
different
populations
in
brain
under
both
physiological
pathological
conditions
remain,
at
least
to
certain
extent,
unresolved.
To
tackle
important
questions,
broad
range
depletion
approaches
been
developed
which
or
(i.e.
NG2-glia
oligodendrocytes)
specifically
ablated
from
adult
network
with
subsequent
analysis
consequences.
As
very
heterogeneous,
it
is
imperative
ablate
single
cell
instead
inducing
death
all
general.
Thanks
modern
genetic
manipulation
methods,
can
now
directly
be
targeted
type
interest
making
ablation
more
specific
compared
general
that
used
earlier
on.
In
this
review
we
will
give
detailed
summary
on
studies,
focusing
mouse
central
nervous
system
(CNS)
functional
readouts.
We
also
provide
an
outlook
how
could
exploited
future.
Brain,
Journal Year:
2015,
Volume and Issue:
138(3), P. 604 - 615
Published: Jan. 8, 2015
Although
substantial
evidence
has
established
that
microglia
and
astrocytes
play
a
key
role
in
the
establishment
maintenance
of
persistent
pain
animal
models,
glial
cells
human
disorders
remains
unknown.
Here,
using
novel
technology
integrated
positron
emission
tomography-magnetic
resonance
imaging
recently
developed
radioligand
(11)C-PBR28,
we
show
increased
brain
levels
translocator
protein
(TSPO),
marker
activation,
patients
with
chronic
low
back
pain.
As
Ala147Thr
polymorphism
TSPO
gene
affects
binding
affinity
for
nine
patient-control
pairs
were
identified
from
larger
sample
subjects
screened
genotyped,
compared
matched-pairs
design,
which
each
patient
was
matched
to
polymorphism-,
age-
sex-matched
control
subject
(seven
Ala/Ala
two
Ala/Thr,
five
males
four
females
group;
median
age
difference:
1
year;
range:
29-63
28-65
controls).
Standardized
uptake
values
normalized
whole
significantly
higher
than
controls
multiple
regions,
including
thalamus
putative
somatosensory
representations
lumbar
spine
leg.
The
thalamic
negatively
correlated
clinical
circulating
proinflammatory
citokine
interleukin-6,
suggesting
expression
exerts
pain-protective/anti-inflammatory
effects
humans,
as
predicted
by
studies.
Given
activated
glia
or
pain,
present
findings
offer
implications
may
serve
guide
future
studies
pathophysiology
management
variety
conditions.
Frontiers in Cellular Neuroscience,
Journal Year:
2018,
Volume and Issue:
12
Published: April 27, 2018
In
a
state
of
oxidative
stress,
there
is
an
increase
reactive
species,
which
induce
altered
intracellular
signaling,
leading
to
dysregulation
the
inflammatory
response.
The
inability
antioxidant
defense
systems
modulate
proinflammatory
response
key
onset
and
progression
neurodegenerative
diseases.
aim
this
work
review
effect
stress
on
loss
regulation
microglia
astrocytes,
induction
different
CD4+T
cell
populations
in
neuroinflammation,
as
well
its
role
some
For
purpose,
intentional
search
original
articles,
short
communications,
reviews,
was
carried
out
following
databases:
PubMed,
Scopus,
Google
Scholar.
articles
reviewed
included
period
from
1997
2017.
With
evidence
obtained,
we
conclude
that
redox
balance
induces
alterations
differentiation
number
subpopulations,
Th1
Th17
This
contributes
development
neuroinflammation
diseases
such
Alzheimer's
(AD),
Parkinson's
(PD),
Multiple
Sclerosis
(MS).
contrast,
regulatory
T
cells
(Tregs)
Th2
cells,
microglia,
astrocytes.
respect,
it
has
been
found
mobilization
with
anti-inflammatory
characteristics
toward
damaged
regions
CNS
can
provide
neuroprotection
become
therapeutic
strategy
control
processes
neurodegeneration.