Nature Aging,
Год журнала:
2022,
Номер
2(9), С. 837 - 850
Опубликована: Сен. 20, 2022
Abstract
Microglia
and
complement
can
mediate
neurodegeneration
in
Alzheimer’s
disease
(AD).
By
integrative
multi-omics
analysis,
here
we
show
that
astrocytic
microglial
proteins
are
increased
Tau
P301S
synapse
fractions
with
age
a
C1q-dependent
manner.
In
addition
to
microglia,
identified
astrocytes
contribute
substantially
elimination
hippocampi.
Notably,
found
relatively
more
excitatory
marker
lysosomes,
whereas
lysosomes
contained
inhibitory
material.
C1q
deletion
reduced
astrocyte–synapse
association
decreased
synapses
engulfment
mice
rescued
density.
Finally,
an
AD
mouse
model
combines
β-amyloid
pathologies,
of
the
risk
gene
Trem2
impaired
phagocytosis
synapses,
engulfed
around
plaques.
Together,
our
data
reveal
contact
eliminate
manner
thereby
pathological
loss
compensate
for
dysfunction.
Science,
Год журнала:
2018,
Номер
362(6411), С. 181 - 185
Опубликована: Окт. 11, 2018
Glia
constitute
roughly
half
of
the
cells
central
nervous
system
(CNS)
but
were
long-considered
to
be
static
bystanders
its
formation
and
function.
Here
we
provide
an
overview
how
diverse
dynamic
functions
glial
orchestrate
essentially
all
aspects
Radial
glia,
astrocytes,
oligodendrocyte
progenitor
cells,
oligodendrocytes,
microglia
each
influence
development,
from
neuronal
birth,
migration,
axon
specification,
growth
through
circuit
assembly
synaptogenesis.
As
neural
circuits
mature,
distinct
glia
fulfill
key
roles
in
synaptic
communication,
plasticity,
homeostasis,
network-level
activity
monitoring
alteration
CNS
structure
Continued
elucidation
cell
biology,
interactions
neurons
will
enrich
our
understanding
formation,
health,
Nature Communications,
Год журнала:
2020,
Номер
11(1)
Опубликована: Март 5, 2020
Abstract
Astrocytes,
a
major
cell
type
found
throughout
the
central
nervous
system,
have
general
roles
in
modulation
of
synapse
formation
and
synaptic
transmission,
blood–brain
barrier
formation,
regulation
blood
flow,
as
well
metabolic
support
other
brain
resident
cells.
Crucially,
emerging
evidence
shows
specific
adaptations
astrocyte-encoded
functions
regions,
such
spinal
cord
cerebellum.
To
investigate
true
extent
astrocyte
molecular
diversity
across
forebrain
we
used
single-cell
RNA
sequencing.
Our
analysis
identifies
five
transcriptomically
distinct
subtypes
adult
mouse
cortex
hippocampus.
Validation
our
data
situ
reveals
spatial
positioning
defined
subtypes,
reflecting
distribution
morphologically
physiologically
populations.
findings
are
for
specialized
between
within
regions.
The
available
through
an
online
database
(
https://holt-sc.glialab.org/
),
providing
resource
on
which
to
base
explorations
local
function
brain.
Trends in Immunology,
Год журнала:
2020,
Номер
41(9), С. 758 - 770
Опубликована: Авг. 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
Molecular Psychiatry,
Год журнала:
2019,
Номер
25(1), С. 148 - 167
Опубликована: Авг. 7, 2019
Alzheimer’s
disease
is
a
devastating
neurodegenerative
disorder
with
no
cure.
Countless
promising
therapeutics
have
shown
efficacy
in
rodent
models
yet
failed
to
benefit
human
patients.
While
hope
remains
that
earlier
intervention
existing
will
improve
outcomes,
it
becoming
increasingly
clear
new
approaches
understand
and
combat
the
pathophysiology
of
are
needed.
Human
induced
pluripotent
stem
cell
(iPSC)
technologies
changed
face
preclinical
research
iPSC-derived
types
being
utilized
study
an
array
conditions,
including
disease.
All
major
brain
can
now
be
differentiated
from
iPSCs,
while
complex
co-culture
systems
developed
facilitate
neuroscience
research.
Many
cellular
functions
perturbed
recapitulated
using
cells
vitro,
platforms
beginning
yield
insights
into
interactions
occur
between
during
neurodegeneration.
Further,
iPSC-based
genome
editing
tools
critical
understanding
roles
numerous
genes
mutations
found
modify
risk
past
decade.
still
their
relative
infancy,
these
developing
hold
considerable
promise
push
forward
efforts
other
disorders.
Frontiers in Immunology,
Год журнала:
2020,
Номер
11
Опубликована: Июль 16, 2020
Based
on
discoveries
enabled
by
new
technologies
and
analyzed
using
novel
computational
tools,
neuroscience
can
be
re-conceived
in
terms
of
information
exchange
dense
networks
intercellular
connections
rather
than
the
context
individual
populations,
such
as
glia
or
neurons..
Cross-talk
between
neurons
microglia
astrocytes
are
has
been
addressed,
however,
manner
which
non-neuronal
cells
communicate
interact
remains
less
well
understood.
We
review
this
intriguing
crosstalk
among
CNS
cells,
focusing
how
it
contributes
to
brain
development
two
neurodegenerative
diseases:
Alzheimer
disease
GRN-FTLD
most
prevalent
tumor,
astrocytoma.
The
goal
studying
these
communications
is
promote
our
ability
combat
incurable
neurological
disorders.
Frontiers in Cellular Neuroscience,
Год журнала:
2020,
Номер
14
Опубликована: Март 19, 2020
A
plethora
of
neurological
disorders
shares
a
final
common
deadly
pathway
known
as
excitotoxicity.
Among
these
disorders,
ischemic
injury
is
prominent
cause
death
and
disability
worldwide.
Brain
ischemia
stems
from
cardiac
arrest
or
stroke,
both
responsible
for
insufficient
blood
supply
to
the
brain
parenchyma.
Glucose
oxygen
deficiency
disrupts
oxidative
phosphorylation,
which
results
in
energy
depletion
ionic
imbalance,
followed
by
cell
membrane
depolarization,
calcium
(Ca2+)
overload,
extracellular
accumulation
excitatory
amino
acid
glutamate.
If
tight
physiological
regulation
fails
clear
surplus
this
neurotransmitter,
subsequent
prolonged
activation
glutamate
receptors
forms
vicious
circle
between
elevated
concentrations
intracellular
Ca2+
ions
aberrant
release,
aggravating
effect
pathway.
The
downstream
Ca2+-dependent
enzymes
has
catastrophic
impact
on
nervous
tissue
leading
death,
accompanied
formation
free
radicals,
edema,
inflammation.
After
decades
"neuron-centric"
approaches,
recent
research
also
finally
shed
some
light
role
glial
cells
diseases.
It
becoming
more
evident
that
neurons
glia
depend
each
other.
Neuronal
cells,
astrocytes,
microglia,
NG2
glia,
oligodendrocytes
all
have
their
roles
what
However,
who
main
contributor
pathway,
unsuspecting
victim?
In
review
article,
we
summarize
so-far-revealed
central
system,
with
particular
attention
ischemia-induced
excitotoxicity,
its
origins,
consequences.
Annual Review of Neuroscience,
Год журнала:
2019,
Номер
42(1), С. 107 - 127
Опубликована: Июль 8, 2019
Maturation
of
neuronal
circuits
requires
selective
elimination
synaptic
connections.
Although
neuron-intrinsic
mechanisms
are
important
in
this
process,
it
is
increasingly
recognized
that
glial
cells
also
play
a
critical
role.
Without
proper
functioning
these
cells,
the
number,
morphology,
and
function
contacts
profoundly
altered,
resulting
abnormal
connectivity
behavioral
abnormalities.
In
addition
to
their
role
refinement,
have
been
implicated
pathological
synapse
loss
dysfunction
following
injury
or
nervous
system
degeneration
adults.
regulating
glia-mediated
still
being
uncovered,
clear
complex
process
involves
many
cues
promote
inhibit
removal
specific
Gaining
greater
understanding
signals
contribution
different
cell
types
will
not
only
provide
insight
into
biological
event
but
be
instrumental
advancing
knowledge
brain
development
neural
disease.
Nature Communications,
Год журнала:
2018,
Номер
9(1)
Опубликована: Апрель 18, 2018
Abstract
Non-pial
neocortical
astrocytes
have
historically
been
thought
to
comprise
largely
a
nondiverse
population
of
protoplasmic
astrocytes.
Here
we
show
that
the
mouse
somatosensory
cortex
manifest
layer-specific
morphological
and
molecular
differences.
Two-
three-dimensional
observations
revealed
in
different
layers
possess
distinct
morphologies
as
reflected
by
differences
cell
orientation,
territorial
volume,
arborization.
The
extent
ensheathment
synaptic
clefts
layer
II/III
was
greater
than
those
VI.
Moreover,
gene
expression
were
observed
between
upper-layer
deep-layer
Importantly,
astrocyte
properties
abrogated
reeler
Dab1
conditional
knockout
mice,
which
neuronal
are
disturbed,
suggesting
prerequisite
for
This
study
thus
demonstrates
existence
interactions
neurons
astrocytes,
may
underlie
their
functions.