Astrocytes
participate
in
numerous
aspects
of
central
nervous
system
(CNS)
physiology
ranging
from
ion
balance
to
metabolism,
and
disruption
their
physiological
roles
can
therefore
be
a
contributor
CNS
dysfunction
pathology.
Cellular
senescence,
one
the
mechanisms
aging,
has
been
proposed
as
component
age
dependency
neurodegenerative
disorders.
Cumulative
evidence
supports
an
integral
role
astrocytes
initiation
progression
disease
cognitive
decline
with
aging.
The
loss
astrocyte
function
or
gain
neuroinflammatory
result
cellular
senescence
could
have
profound
implications
for
aging
brain
disorders,
we
propose
term
"astrosenescence"
describe
this
phenotype.
This
review
summarizes
current
pertaining
early
evidence,
vitro
characterization
relationship
age-related
disease.
We
discuss
significance
targeting
senescent
novel
approach
toward
therapies
age-associated
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
Annual Review of Neuroscience,
Год журнала:
2019,
Номер
42(1), С. 187 - 207
Опубликована: Июль 8, 2019
Astrocytes
are
morphologically
complex,
ubiquitous
cells
that
viewed
as
a
homogeneous
population
tiling
the
entire
central
nervous
system
(CNS).
However,
this
view
has
been
challenged
in
last
few
years
with
availability
of
RNA
sequencing,
immunohistochemistry,
electron
microscopy,
morphological
reconstruction,
and
imaging
data.
These
studies
suggest
astrocytes
represent
diverse
they
display
brain
area–
disease–specific
properties
functions.
In
review,
we
summarize
these
observations,
emphasize
areas
where
clear
conclusions
can
be
made,
discuss
potential
unifying
themes.
We
also
identify
knowledge
gaps
need
to
addressed
order
exploit
astrocyte
diversity
biological
phenomenon
physiological
relevance
CNS.
thus
provide
summary
perspective
on
vertebrate
Acta Physiologica,
Год журнала:
2020,
Номер
229(3)
Опубликована: Март 29, 2020
The
new
coronavirus,
classified
as
severe
acute
respiratory
syndrome
(SARS)-CoV-2
that
emerged
in
Hubei
province
China,
causes
a
coronavirus
disease,
which
was
termed
COVID-19
by
WHO
on
11
February
2020.
claimed
more
than
65
000
lives
around
the
world
5th
of
April
It
is
not
first
infects
humans;
pathogenic
viruses
cause
human
diseases
(human
coronaviruses,
HCoV)
include
6
other
members
designated
SARS-CoV,
middle
east
(MERS)-CoV,
HCoV-HKU1,
HCoV-NL63,
HCoV-OC43
and
HCoV-229E.
clinical
presentation
mainly
manifested
malignant
pneumonia;
although
many
patients
present
neurological
symptoms,
such
vomiting,
dizziness,
headache
delirium.1
Human
coronaviruses
were
identified
mid-1960s;
they
named
for
crown-like
spikes
their
surface.
SARS-CoV-2
virus
belongs
to
β-coronavirus,
also
MERS-CoV,
SARS-CoV-1,
NCoV-OC43
HCoV-HKU1.
primary
target
cells
are
epithelial
gastrointestinal
tract,
contain
angiotensin
converting
enzyme
2
(ACE2),
utilized
enter
cell;
it
is,
however,
hard
believe
penetration
viral
agent
into
organism
limited
only
these
tissues.2
Clinical
pre-clinical
data
from
studies
with
suggest
wider
tissue
invasiveness
an
evident
neurotropism,
may
result
complex
scenarios.
Can
central
nervous
system
(CNS)
infect
neural
cells?
And
if
yes,
how
CNS
damage
contributes
pathophysiology
COVID-19,
its
signs,
symptoms
progression
well
sequelae.
In
words,
had
significant
could
presence
be
pathophysiologically
relevant?
has
been
demonstrated
especially
β-coronaviruses
belongs,
do
limit
tract
frequently
invade
CNS.
This
propensity
convincingly
documented
MERS-CoV
responsible
porcine
haemagglutinating
encephalomyelitis
(HEV
67N).3-5
Previous
findings
demonstrate
ACE2
represents
key,
but
exclusive,
site
entry
cell.
expressed
brain,
being
particularly
brain
stem
regions
regulation
cardiovascular
function
including
subfornical
organ,
paraventricular
nucleus,
nucleus
tractus
solitarius,
rostral
ventrolateral
medulla;
expression
found
both
neurones
glia.6,
7
Non-ACE2
pathways
infection
cannot
excluded;
marked
liver,
organ
lower
levels
ACE
compared
CNS,
strongly
supports
assumption
cell
routes
can
vary.8
Be
this
all
may,
have
reported2
SARS-CoV-1
tissues
obtained
infected
patients.9
intranasal
administration
SARS-CoV-110
or
MERS-COV11
resulted
rapid
invasion
particles
possibly
through
olfactory
bulb
via
trans-synaptic
route.
pathway
when
enters
peripheral
nerves
spreads
synaptic
contacts
well-documented
several
CoVs.12
brainstem,
hosts
neuronal
circuit
medulla,
severely
types
viruses,
contribute
degradation
failure
centres.
When
nasal
infecting
charges
delivered
extremely
low
doses,
colonized,
absent
lungs,11
corroborating
potent
neurotropism
coronarovirus
strains.
testifies
property
ignored
complete
understanding
impact
organism.
Although
direct
evidence
currently
lacking,
high
identity
between
suggests,
latter
strain
ability
clearly
family
belong.
β-coronavirus
NCoV-OC43,
upper
disorder,
lines
culture;
encephalitis
associated
apoptosis
necrosis
mice.13
At
least
two
cases
encephalitis/encepahlomyelitis
caused
reported.14,
15
About
12%
children
hospitalised
at
Children's
Hospital
Chenzhou,
China
May
2014
2015
anti-CoV
antibodies
serum
cerebrospinal
fluid.16
considerable
interest
distribution
shown
cerebrum,
cerebellum.17
These
parts
exhibit
distinct
ratios
neuroglia;
neocortex
number
non-neuronal
(most
represented
neuroglia)
almost
four
times
larger
neurones,
whereas
cerebellum
account
~90%
cells.18
Upon
because
forms
neuroglial
become
reactive,
representing
most
classic
neuropathological
scenario
ongoing
neuroinflammation.
Therefore,
possible
triggers
reactive
astrogliosis
activation
microglia.
framework,
learned
Tick-borne
(TBEV)
Zika
(ZIKV),
predicts
strong
role
astrocytes
microglia
orchestrating
response
neuroinfection
spread
brain.
One
fundamental
events
pathogen
crossing
blood-brain
barrier
(BBB).
Astrocytes
form
parenchymal
portion
BBB
endfeet,
extensively
plaster
(~98%
coverage)
intracranial
blood
vessels.
grey
mater
occupy
separate
territorial
domains
integrate
elements
vasculature
forming
neurovascular
unit.19
Both
TBEV
ZIKV
belong
Flaviviridae
family,
endocytosis20,
21
thus
instigating
neuroinfection.
Internalization
mediated
clathrin-dependent
endocytosis
known
West
Nile
virus,
Dengue
Hepatitis
C
Bovine
Viral
Diarrhoea
virus.21
Whether
SARS-Co-V2
astroglial
remains
studied,
interneuronal
transfer
another
HEV67
utilises
endocytotic/exocytotic
pathway.4
rodent
no
detrimental
effect
viability
hence
likely
represent
reservoir
where
further
re-infection
occur.
Once
within
cell,
traffic
different
compartments.
astroglia
uses
endosomal
cytoplasm.22
virus-loaded
vesicles
exhibits
directional
mobility,
driven
protein
motors
carrying
along
cytoskeletal
elements,
microtubules,
actin
intermediate
filaments.
On
hand,
non-directional
characterized
randomness
free
diffusion.
As
time,
there
series
virus-infected
cells,
leading
increased
per
astrocytes,
pronounced
increase
particle
mobility.22
Similar
infiltration
TBEV,
recently
confirmed
mechanism
microglia.23
Among
susceptible
released
progeny
tolerated
higher
loads
neurones.20
occurrence
affect
chemosensing
centre
damaging
ventilatory
lung
function.
Further
support
hypothesis
route
organism,
provided
observations
early
profound
anosmia
subjects
(Ear,
Nose
Throat
surgery
society,
ENT
UK;
https://www.entuk.org/sites/default/files/files/LossofsenseofsmellasmarkerofCOVID.pdf).
Another
aspect
SARS
CoV2
substantial
systemic
inflammatory
storm
massive
release
cytokines,
chemokines,
inflammation
signals
subsequent
break
BBB,
instigates
amplifies
neuroinflammatory
process.
Numerous
preclinical
consistently
inflammation,
regardless
nature,
bacterial,
toxic,
compromises
injures
glia
limitans,
activates
Toll-like
receptors
residing
innate
immunity,
ultimately
promoting
neuroinflammation
disturb
homeostasis
death.24
process
functional
explain
experience
according
even
who
overcome
pneumonia,
onset
cognitive
impairment
behavioural
changes
observed.
Delirium
deficits
abnormalities
situation
conditions
prolonged
hypoxia
induces
persistent
uncontrolled
neuroinflammation—responsible,
turn,
hippocampus
cortical
areas
functions
alterations.25
Elderly
recovering
pneumonia
often
delirium
attention
memory
persist
over
time
require
treatment,
remarkably
demanding.
commonly
provoked
inflammation.
Elevated
concentrations
pro-interleukins
S100B,
(recognized
index
disruption),
observed
during
elderly
patients.26
Neuroinflammation
appears
obligatory
component
neurodegenerative
disorders27
implicated
psychiatric
pathologies
psychosis
schizophrenia,
autism
spectrum
affective
disorders
name
few.28
There
association
depressive
syndromes
infections
rising
risk
episodes
~60%.28
animal
models,
injections
cytokines
sickness
behaviour29;
very
similar
"flu-like
syndrome"
anhedonia,
anorexia,
fever,
fatigue,
pain,
sleep
disturbances,
confusion.
Furthermore,
accompanying
long-lasting
hypoxia,
arguably
affects
neurocognitive
alterations.
To
conclude:
neurotropic,
exception;
routes,
notably
inoculation
though
using
pathways.
Coronaviruses
express
ACE2,
endocytotic
(similar
those
ZIKA
viruses)
excluded.
Coronavirueses
predominantly
nuclei
cardio-respiratory
control;
injuries
exacerbate
lead
failure.
Direct
together
accompanies
promote
neuropsychiatric
developments
impairments
chronic.
aspects
attack
must
therefore
considered
designing
therapeutic
strategies
rehabilitation
paradigms
aimed
victims
SARS-CoV-2.
No
conflict
declare.
Frontiers in Aging Neuroscience,
Год журнала:
2019,
Номер
11
Опубликована: Март 19, 2019
Astrocytes,
one
of
the
largest
glial
cell
population
in
Central
Nervous
System,
play
key
function
several
events
brain
development
and
function,
such
as
synapse
formation
control
neurotransmitters
release
uptake,
production
trophic
factors
neuronal
survival.
Initially
described
a
homogenous
population,
evidences
have
pointed
that
astrocytes
are
highly
heterogeneous,
both
morphologically
functionally,
within
same
region,
across
different
regions.
Recent
findings
suggest
heterogeneity
expression
profile
proteins
involved
astrocyte
may
predict
selective
vulnerability
regions
to
specific
diseases,
well
age-related
cognitive
decline.
However,
molecular
mechanisms
underlying
these
changes,
either
aging
disease
scarce.
Neuroinflammation,
hallmark
neurodegenerative
diseases
aging,
is
reported
dubious
impact
on
activation,
cells
pro-
anti-inflammatory
cytokines
chemokines,
anti-oxidants,
free
radicals,
neurotrophic
factors.
Despite
emerging
evidence
supporting
reactive
duality
their
phenotype,
neurotoxic
or
neuroprotective
properties,
depending
age
stimuli,
cellular
interplays
regional
still
matter
discussion.
In
this
review,
we
will
summarize
recent
phenotypes,
likely
for
during
neural
diseases.
We
focus
molecules
triggered
by
Finally,
discuss
new
how
modulation
phenotype
could
synaptic
deficits
dysfunction
present
pathological
states.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Июнь 26, 2023
Abstract
Spinal
cord
injury
(SCI)
remains
a
severe
condition
with
an
extremely
high
disability
rate.
The
challenges
of
SCI
repair
include
its
complex
pathological
mechanisms
and
the
difficulties
neural
regeneration
in
central
nervous
system.
In
past
few
decades,
researchers
have
attempted
to
completely
elucidate
mechanism
identify
effective
strategies
promote
axon
circuit
remodeling,
but
results
not
been
ideal.
Recently,
new
SCI,
especially
interactions
between
immune
cell
responses,
revealed
by
single-cell
sequencing
spatial
transcriptome
analysis.
With
development
bioactive
materials
stem
cells,
more
attention
has
focused
on
forming
intermediate
networks
reconstruction
than
promoting
axonal
corticospinal
tract.
Furthermore,
technologies
control
physical
parameters
such
as
electricity,
magnetism
ultrasound
constantly
innovated
applied
fate
regulation.
Among
these
advanced
novel
technologies,
therapy,
biomaterial
transplantation,
electromagnetic
stimulation
entered
into
stage
clinical
trials,
some
them
already
treatment.
this
review,
we
outline
overall
epidemiology
pathophysiology
expound
latest
research
progress
related
detail,
propose
future
directions
for
applications.
International Journal of Biological Sciences,
Год журнала:
2021,
Номер
17(9), С. 2181 - 2192
Опубликована: Янв. 1, 2021
Extracellular
neuritic
plaques
composed
of
amyloid‑β
(Aβ)
protein
and
intracellular
neurofibrillary
tangles
containing
phosphorylated
tau
are
the
two
hallmark
proteins
Alzheimer's
disease
(AD),
separate
neurotoxicity
these
in
AD
has
been
extensively
studied.
However,
interventions
that
target
Aβ
or
individually
have
not
yielded
substantial
breakthroughs.
The
interest
interactions
between
is
increasing,
but
related
drug
investigations
their
infancy.
This
review
discusses
how
accelerates
phosphorylation
possible
mechanisms
pathways
by
which
mediates
toxicity.
also
describes
synergistic
effects
on
microglial
cells
astrocytes.
Studies
suggest
coexistence
to
mechanism
facilitates
propagation
aggregation
plaques.
mediate
cognitive
dysfunction
patients
with
AD.
In
summary,
this
summarizes
recent
data
interplay
promote
a
better
understanding
roles
pathological
process
provide
new
insights
into
against