Frontiers in Aging Neuroscience,
Journal Year:
2018,
Volume and Issue:
10
Published: July 17, 2018
The
biology
of
brain
microvascular
pericytes
is
an
active
area
research
and
discovery,
as
their
interaction
with
the
endothelium
critical
for
multiple
aspects
cerebrovascular
function.
There
growing
evidence
that
pericyte
loss
or
dysfunction
involved
in
pathogenesis
Alzheimer's
disease,
vascular
dementia,
ischemic
stroke
injury.
However,
strategies
to
mitigate
compensate
this
remain
limited.
In
review,
we
highlight
a
novel
finding
adult
are
structurally
dynamic
vivo,
actively
endothelial
coverage
by
extending
far-reaching
processes
maintain
contact
regions
exposed
endothelium.
Structural
remodeling
may
present
opportunity
foster
pericyte-endothelial
communication
should
be
explored
potential
means
counteract
dementia
disease.
We
discuss
pathophysiological
consequences
on
capillary
function,
biochemical
pathways
control
remodeling.
also
offer
guidance
observing
such
structural
can
more
broadly
studied
mouse
models
Journal of Cerebral Blood Flow & Metabolism,
Journal Year:
2020,
Volume and Issue:
40(1_suppl), P. S6 - S24
Published: Sept. 14, 2020
The
blood–brain
barrier
(BBB)
is
a
critical
regulator
of
CNS
homeostasis.
It
possesses
physical
and
biochemical
characteristics
(i.e.
tight
junction
protein
complexes,
transporters)
that
are
necessary
for
the
BBB
to
perform
this
physiological
role.
Microvascular
endothelial
cells
require
support
from
astrocytes,
pericytes,
microglia,
neurons,
constituents
extracellular
matrix.
This
intricate
relationship
implies
existence
neurovascular
unit
(NVU).
NVU
cellular
components
can
be
activated
in
disease
contribute
dynamic
remodeling
BBB.
especially
true
resident
immune
brain,
which
polarize
into
distinct
proinflammatory
(M1)
or
anti-inflammatory
(M2)
phenotypes.
Current
data
indicate
M1
pro-inflammatory
microglia
dysfunction
vascular
“leak”,
while
M2
play
protective
role
at
Understanding
biological
mechanisms
involved
activation
provides
unique
opportunity
develop
novel
treatment
approaches
neurological
diseases.
In
review,
we
highlight
describe
how
these
phenotypes
modulate
physiology.
Additionally,
outline
other
cell
types
regulating
microglial
targeted
with
focus
on
ischemic
stroke
Alzheimer’s
disease.
Acta Neuropathologica,
Journal Year:
2018,
Volume and Issue:
136(4), P. 507 - 523
Published: Aug. 10, 2018
Many
central
nervous
system
diseases
currently
lack
effective
treatment
and
are
often
associated
with
defects
in
microvascular
function,
including
a
failure
to
match
the
energy
supplied
by
blood
used
on
neuronal
computation,
or
breakdown
of
blood–brain
barrier.
Pericytes,
an
under-studied
cell
type
located
capillaries,
crucial
importance
regulating
diverse
functions,
such
as
angiogenesis,
barrier,
capillary
flow
movement
immune
cells
into
brain.
They
also
form
part
"glial"
scar
isolating
damaged
parts
CNS,
may
have
stem
cell-like
properties.
Recent
studies
suggested
that
pericytes
play
role
neurological
diseases,
thus
therapeutic
target
disorders
stroke,
traumatic
brain
injury,
migraine,
epilepsy,
spinal
cord
diabetes,
Huntington's
disease,
Alzheimer's
multiple
sclerosis,
glioma,
radiation
necrosis
amyotrophic
lateral
sclerosis.
Here
we
report
recent
advances
our
understanding
pericyte
biology
discuss
how
could
be
targeted
develop
novel
approaches
disorders,
increasing
flow,
preserving
barrier
entry
modulating
formation
vessels
in,
glial
around,
regions.
Proceedings of the National Academy of Sciences,
Journal Year:
2020,
Volume and Issue:
117(43), P. 27022 - 27033
Published: Oct. 13, 2020
The
essential
function
of
the
circulatory
system
is
to
continuously
and
efficiently
supply
O2
nutrients
necessary
meet
metabolic
demands
every
cell
in
body,
a
which
vast
capillary
networks
play
key
role.
Capillary
serve
an
additional
important
central
nervous
system:
acting
as
sensory
network,
they
detect
neuronal
activity
form
elevated
extracellular
K+
initiate
retrograde,
propagating,
hyperpolarizing
signal
that
dilates
upstream
arterioles
rapidly
increase
local
blood
flow.
Yet,
little
known
about
how
entering
this
network
distributed
on
branch-to-branch
basis
reach
specific
neurons
need.
Here,
we
demonstrate
capillary-enwrapping
projections
junctional,
contractile
pericytes
within
postarteriole
transitional
region
differentially
constrict
structurally
dynamically
determine
morphology
junctions
thereby
regulate
branch-specific
We
further
found
these
are
capable
receiving
propagating
K+-induced
signals
through
channeling
red
cells
toward
initiating
signal.
By
controlling
flow
at
junctions,
functionally
distinct
maintain
efficiency
effectiveness
enabling
optimal
perfusion
brain.
Cellular and Molecular Life Sciences,
Journal Year:
2018,
Volume and Issue:
76(6), P. 1081 - 1092
Published: Dec. 6, 2018
The
blood–brain
barrier
is
a
dynamic
multicellular
interface
that
regulates
the
transport
of
molecules
between
blood
circulation
and
brain
parenchyma.
Proteins
peptides
required
for
homeostasis
cross
via
transcellular
transport,
but
mechanisms
control
this
pathway
are
not
well
characterized.
Here,
we
highlight
recent
studies
on
intracellular
transcytosis
across
barrier.
Endothelial
cells
at
possess
an
intricate
endosomal
network
allows
sorting
to
diverse
cellular
destinations.
Internalization
from
plasma
membrane,
sorting,
exocytosis
all
contribute
regulation
transcytosis.
Transmembrane
receptors
blood-borne
proteins
utilize
different
pathways
endothelial
cells.
Alterations
in
during
diseases
central
nervous
system
disruption
disease
progression.
Harnessing
can
help
improve
delivery
biotherapeutics
brain.
Frontiers in Immunology,
Journal Year:
2020,
Volume and Issue:
11
Published: Dec. 16, 2020
Chimeric
antigen
receptor
(CAR)
T
cells
provide
new
therapeutic
options
for
patients
with
relapsed/refractory
hematologic
malignancies.
However,
neurotoxicity
is
a
frequent,
and
potentially
fatal,
complication.
The
spectrum
of
manifestations
ranges
from
delirium
language
dysfunction
to
seizures,
coma,
fatal
cerebral
edema.
This
novel
syndrome
has
been
designated
immune
effector
cell-associated
(ICANS).
In
this
review,
we
draw
an
arc
our
current
understanding
how
systemic
local
cytokine
release
act
on
the
CNS,
toward
possible
preventive
approaches.
We
systematically
review
reported
correlations
secreted
inflammatory
mediators
in
serum/plasma
cerebrospinal
fluid
risk
ICANS
receiving
CAR
cell
therapy.
Possible
pathophysiologic
impacts
CNS
are
covered
detail
most
promising
candidate
cytokines,
including
IL-1,
IL-6,
IL-15,
GM-CSF.
To
insight
into
final
common
pathways
inflammation,
place
context
other
conditions
that
associated
neurologic
dysfunction,
sepsis-associated
encephalopathy,
malaria,
thrombotic
microangiopathy,
infections,
hepatic
encephalopathy.
then
what
known
about
interaction
components
neurovascular
unit,
endothelial
cells,
pericytes,
astrocytes,
microglia
neurons
respond
challenges.
Current
approaches,
corticosteroids
blockade
IL-1
IL-6
signaling,
reviewed
role
cytokines
ICANS.
Throughout,
point
out
gaps
knowledge
approaches
investigation
mechanism,
prevention,
treatment
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(5), P. 2681 - 2681
Published: March 6, 2021
Emerging
data
indicate
that
neurological
complications
occur
as
a
consequence
of
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
infection.
The
blood–brain
barrier
(BBB)
is
critical
interface
regulates
entry
circulating
molecules
into
the
CNS,
and
regulated
by
signals
arise
from
brain
blood
compartments.
In
this
review,
we
discuss
mechanisms
which
SARS-CoV-2
interactions
with
BBB
may
contribute
to
dysfunction
associated
disease
2019
(COVID-19),
caused
SARS-CoV-2.
We
consider
aspects
peripheral
disease,
such
hypoxia
systemic
inflammatory
response
syndrome/cytokine
storm,
well
CNS
infection
viral
brain.
also
contribution
risk
factors
for
developing
COVID-19
could
increase
or
otherwise
damage
Annual Review of Physiology,
Journal Year:
2021,
Volume and Issue:
84(1), P. 331 - 354
Published: Oct. 21, 2021
The
vast
majority
of
the
brain's
vascular
length
is
composed
capillaries,
where
our
understanding
blood
flow
control
remains
incomplete.
This
review
synthesizes
current
knowledge
on
across
microvascular
zones
by
addressing
issues
with
nomenclature
and
drawing
new
developments
from
in
vivo
optical
imaging
single-cell
transcriptomics.
Recent
studies
have
highlighted
important
distinctions
mural
cell
morphology,
gene
expression,
contractile
dynamics,
which
can
explain
observed
differences
response
to
vasoactive
mediators
between
arteriole,
transitional,
capillary
zones.
Smooth
muscle
cells
arterioles
ensheathing
pericytes
arteriole-capillary
transitional
zone
large-scale,
rapid
changes
flow.
In
contrast,
downstream
act
slower
smaller
scales
are
involved
establishing
resting
tone
heterogeneity.
Many
unresolved
remain,
including
that
activate
different
pericyte
types
vivo,
role
pericyte-endothelial
communication
conducting
signals
capillaries
arterioles,
how
neurological
disease
affects
these
mechanisms.