Frontiers in Molecular Neuroscience,
Год журнала:
2023,
Номер
16
Опубликована: Июнь 23, 2023
Classic
experiments
with
peripheral
sympathetic
neurons
established
an
absolute
dependence
upon
NGF
for
survival.
A
forgotten
problem
is
how
these
become
resistant
to
deprivation
of
trophic
factors.
The
question
whether
and
can
survive
in
the
absence
support.
However,
mechanism
not
understood
switch
their
phenotype
lose
on
factors,
such
as
BDNF.
Here,
we
approach
by
considering
requirements
support
hippocampal
from
central
nervous
system.
We
developed
cellular
assays
assess
factor
dependency
identified
factors
that
rescue
They
include
enhanced
expression
a
subunit
receptor
(Neurotrophin
Receptor
Homolog,
NRH)
increase
glucocorticoid
neurons.
results
are
significant
since
levels
activity
responsible
many
neuropsychiatric
conditions.
Resistance
may
be
relevant
underlying
basis
longevity,
well
important
element
preventing
neurodegeneration.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(2), С. 1688 - 1688
Опубликована: Янв. 14, 2023
It
has
been
proposed
that
mechanosensitive
Piezo1
channels
trigger
migraine
pain
in
trigeminal
nociceptive
neurons,
but
the
mechanosensitivity
of
satellite
glial
cells
(SGCs)
supporting
neuronal
sensitization
not
tested
before.
Moreover,
tools
to
monitor
previous
activation
are
available.
Therefore,
by
using
live
calcium
imaging
with
Fluo-4
AM
and
labeling
FM1-43
dye,
we
explored
a
new
strategy
identify
Piezo
channels'
activity
mouse
SGCs,
isolated
meninges.
The
specific
agonist
Yoda1
induced
transients
both
neurons
suggesting
functional
expression
types
cells.
In
Piezo1-transfected
HEK
cells,
produced
only
transient
fluorescent
response,
whereas
co-application
provided
higher
signals
remarkable
long-lasting
'tail
response'.
A
similar
Piezo1-related
trapping
was
observed
SGCs.
non-specific
channel
blocker,
Gadolinium,
inhibited
peak,
confirming
involvement
receptors.
Finally,
demonstrated
meningeal
tissues
3.5
h
after
washout.
Our
data
indicated
SGCs
express
channels,
their
provides
sustained
FM1-43.
This
labelling
can
be
used
ongoing
system,
which
is
implicated
pain.
Cell Reports,
Год журнала:
2023,
Номер
42(10), С. 113128 - 113128
Опубликована: Сен. 23, 2023
Neuronal
swelling
during
cytotoxic
edema
is
triggered
by
Na+
and
Cl−
entry
Ca2+
independent.
However,
the
causes
of
neuronal
death
are
unknown.
Here,
we
investigate
role
large-conductance
Pannexin-1
(Panx1)
channels
in
edema.
Panx1
channel
inhibitors
reduce
delay
voltage-gated
with
veratridine.
downstream
production
reactive
oxygen
species
(ROS)
that
opens
channels.
We
confirm
ROS
activates
currents
whole-cell
electrophysiology
find
scavenging
neuroprotective.
opening
subsequent
ATP
release
attract
microglial
processes
to
contact
neurons.
Depleting
microglia
using
CSF1
receptor
antagonist
PLX3397
or
blocking
P2Y12
receptors
exacerbates
death,
suggesting
Panx1-ATP-dependent
contacts
conclude
triggers
oxidative
stress
neurons
trigger
but
also
initiates
neuroprotective
feedback
mediated
contacts.
Journal of Neuroscience,
Год журнала:
2024,
Номер
44(28), С. e1441232024 - e1441232024
Опубликована: Июнь 3, 2024
The
vagal
ganglia,
comprised
of
the
superior
(jugular)
and
inferior
(nodose)
ganglia
vagus
nerve,
receive
somatosensory
information
from
head
neck
or
viscerosensory
inner
organs,
respectively.
Developmentally,
cranial
neural
crest
gives
rise
to
all
glial
cells
neurons
jugular
while
epibranchial
placode
nodose
ganglia.
Crest-derived
progenitors
can
additionally
generate
autonomic
in
peripheral
nervous
system,
but
how
these
is
unknown.
Here,
we
found
that
some
Sox10+
crest-derived
in,
surrounding,
ganglion
transiently
expressed
Phox2b,
a
master
regulator
system
development,
during
early
embryonic
life.
Our
genetic
lineage-tracing
analysis
mice
either
sex
revealed
despite
their
common
developmental
origin
extreme
spatial
proximity,
substantial
proportion
nodose,
not
neighboring
have
history
Phox2b
expression.
We
used
single-cell
RNA-sequencing
demonstrate
give
major
subtypes
including
Schwann
cells,
satellite
glia,
precursors,
mapped
distribution
by
situ
hybridization.
Lastly,
integration
transcriptomic
similarities
between
dorsal
root
immature
subtypes.
work
demonstrates
express
entire
complement
display
transcriptional
program
may
underlie
bipotent
nature.
The Journal of Physiology,
Год журнала:
2024,
Номер
unknown
Опубликована: Июнь 21, 2024
Abstract
Autonomic
dysregulation,
including
sympathetic
hyperactivity,
is
a
common
feature
of
hypertension
(HT)
and
other
cardiovascular
diseases.
The
CNS
plays
role
in
driving
chronic
activation
disease,
but
several
lines
evidence
suggest
that
neuroplasticity
the
periphery
may
also
contribute.
potential
contribution
postganglionic
neurons
to
sustained
hyperactivity
not
well
understood.
We
recently
discovered
noradrenergic
stellate
ganglion
(SG)
have
excitatory
cholinergic
collateral
connections
within
ganglion.
hypothesize
remodelling
these
increased
transmission
contributes
diseases,
HT.
To
test
hypothesis,
we
examined
activity
isolated
SG
under
control
conditions
after
1
week
HT
induced
by
peripheral
angiotensin
II
infusion,
using
whole‐cell
patch
clamp
recordings.
Despite
absence
central
inputs,
observed
elevated
spontaneous
synaptic
from
hypertensive
mice
required
generation
action
potentials.
Genetically
disrupting
decreased
basal
neuronal
prevented
II‐mediated
enhancement
activity.
Similar
changes
activity,
driven
transmission,
were
identified
cardiac
projecting
brown
adipose
tissue.
These
altered
A‐type
K
+
currents.
This
suggests
stimulates
throughout
intraganglionic
network
connections,
contributing
characteristic
disease.
image
Key
points
Sympathetic
ganglia
II‐treated
are
more
active
than
despite
activation.
enhanced
result
ganglionic
collaterals,
rather
intrinsic
excitability.
Increased
was
both
tissue‐projecting
neurons,
which
involved
homeostasis.
Glia,
Год журнала:
2024,
Номер
72(10), С. 1766 - 1784
Опубликована: Июнь 22, 2024
The
central
and
peripheral
nervous
systems
(CNS
PNS,
respectively)
exhibit
remarkable
diversity
in
the
capacity
to
regenerate
following
neuronal
injury
with
PNS
injuries
being
much
more
likely
than
those
that
occur
CNS.
Glial
responses
damage
greatly
influence
likelihood
of
regeneration
by
either
promoting
or
inhibiting
axonal
regrowth
over
time.
However,
despite
our
understanding
how
some
glial
lineages
participate
nerve
degeneration
regeneration,
less
is
known
about
contributions
satellite
cells
(SGC)
failure
axon
branch
dorsal
root
ganglia
(DRG)
sensory
neurons.
Here,
using
vivo,
time-lapse
imaging
larval
zebrafish
coupled
laser
axotomy,
we
investigate
role
SGCs
regeneration.
In
studies
show
respond
relocating
their
nuclei
site
during
same
period
DRG
neurons
produce
new
neurites.
Laser
ablation
prior
results
neurite
growth
attempts
ultimately
a
higher
rate
successful
regrowth,
implicating
as
inhibitors
We
also
demonstrate
this
SGC
response
mediated
part
ErbB
signaling,
chemical
inhibition
receptor
reduced
motility
enhanced
regrowth.
These
findings
provide
insights
into
SGC-neuron
interactions
under
conditions
these
system
repair.
Journal of Neuroendocrinology,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Glial
cells
are
an
integral
component
of
the
nervous
system,
performing
crucial
functions
that
extend
beyond
structural
support,
including
modulation
immune
tissue
repair,
and
maintaining
homeostasis.
Recent
studies
have
highlighted
importance
glial
as
key
mediators
stress
responses
across
different
organs.
This
review
focuses
on
roles
in
peripheral
tissues
health
their
involvement
diseases
linked
to
psychological
stress.
Populations
glia
associated
with
("GAPS")
emerge
a
promising
target
cell
population
our
basic
understanding
stress-associated
pathologies,
highlighting
role
deleterious
effects
various
conditions.
Ultimately,
new
insights
into
impact
populations
periphery
may
support
clinical
efforts
aimed
at
improving
state
patients
for
improved
outcomes.
Korean Journal of Physiology and Pharmacology,
Год журнала:
2023,
Номер
28(1), С. 93 - 103
Опубликована: Дек. 29, 2023
Satellite
glial
cells
(SGCs),
a
major
type
of
cell
in
the
autonomic
ganglia,
closely
envelop
body
and
even
synaptic
regions
single
neuron
with
very
narrow
gap.
This
structurally
unique
organization
suggests
that
neurons
SGCs
may
communicate
reciprocally.
Glial
Ca
Frontiers in Synaptic Neuroscience,
Год журнала:
2022,
Номер
14
Опубликована: Сен. 30, 2022
The
Spontaneously
Hypertensive
Rat
(SHR)
has
increased
sympathetic
drive
to
the
periphery
that
precedes
and
contributes
development
of
high
blood
pressure,
making
it
a
useful
model
for
study
neurogenic
hypertension.
Comparisons
normotensive
Wistar
Kyoto
(WKY)
rat
have
demonstrated
altered
active
intrinsic
properties
SHR
neurons
shortly
before
onset
Here
we
examine
structural
functional
plasticity
postnatal
WKY
cultured
alone
or
co-cultured
with
cardiomyocytes
under
conditions
limited
extrinsic
signaling.
an
number
synaptic
sites
compared
age-matched
neurons,
measured
by
co-localization
presynaptic
vesicular
acetylcholine
transporter
postsynaptic
shank
proteins.
Whole
cell
recordings
show
higher
charge
than
demonstrating
increase
in
is
associated
transmission.
Differences
are
not
firing
rates
between
influenced
interactions
target
from
either
strain.
Both
tonic
patterns
our
cultures,
which
depleted
non-neuronal
ganglionic
cells
provide
neurotrophic
This
suggests
normal
mature,
phasic
requires
signaling,
potentially
differential
responses
prehypertensive
SHR,
been
reported
maintain
at
later
developmental
stages.
While
do
neuronal
differences
display
decreased
hypertrophy
neurons.
These
experiments
suggest
signaling
changes
cardiac-sympathetic
circuit
rats
as
early
period.
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2023,
Номер
unknown
Опубликована: Июль 26, 2023
Neuropeptide
Y
(NPY)
is
best
known
for
its
effects
in
the
brain
as
an
orexigenic
and
anxiolytic
agent
reducing
energy
expenditure.
NPY
also
co-expressed
with
Norepinephrine
(NE)
sympathetic
neurons.
Although
generally
considered
to
modulate
noradrenergic
responses,
specific
roles
autonomic
physiology
remain
under-appreciated.
Here,
we
show
that
sympathetic-derived
essential
metabolic
cardiovascular
regulation
mice.
NE
are
90%
of
prevertebral
neurons
only
43%
paravertebral
NPY-expressing
primarily
innervate
blood
vessels
peripheral
organs.
Sympathetic-specific
deletion
elicits
pronounced
defects
mice,
including
reductions
insulin
secretion,
glucose
tolerance,
cold
pupil
size,
elevation
heart
rate,
while
notably,
however,
basal
pressure
was
unchanged.
These
findings
provide
new
knowledge
about
target
tissue-specific
functions
derived
from
imply
potential
involvement
diseases.