Lateral Ventricular Neural Stem Cells Provide Negative Feedback to Circuit Activation Through GABAergic Signaling
Cells,
Journal Year:
2025,
Volume and Issue:
14(6), P. 426 - 426
Published: March 13, 2025
Recent
studies
have
demonstrated
that
circuit
activation
in
vivo
can
regulate
proliferation
of
lateral
ventricular
neural
stem
cells
(LV
NSCs),
although
the
underlying
molecular
and
cellular
mechanisms
are
not
yet
fully
understood.
Here,
we
investigated
role
GABAergic
signaling
interaction
between
LV
NSCs
anterior
cingulate
cortex-subependymal-choline
acetyltransferase+
(ChAT+)
neuron
(ACC-subep-ChAT+)
circuit.
We
found
monoamine
oxidase
B
(MAOB),
a
key
enzyme
involved
gamma-aminobutyric
acid
(GABA)
synthesis,
is
expressed
NSCs,
ACC-subep-ChAT+
modulate
MAOB
activity.
Additionally,
express
LRRC8D,
core
component
volume-regulated
anion
channels,
GABA
transporter-1
(GAT-1,
SLC6A1).
show
evidence
that,
through
signaling,
LRRC8D
GAT-1
provide
negative
feedback
signal
to
ChAT+
neurons,
NSCs.
These
findings
suggest
MAOB-driven
LRRC8D-regulated
chloride
transport,
GAT-1-facilitated
reuptake
influence
NSC
dynamics
LV.
Language: Английский
Olfactory bulb interneurons – The developmental timeline and targeting defined by embryonic neurogenesis
Molecular and Cellular Neuroscience,
Journal Year:
2025,
Volume and Issue:
unknown, P. 104007 - 104007
Published: March 1, 2025
Language: Английский
Embryonically generated interneurons (EGINs) exhibit a distinctive developmental program and lamination in the olfactory bulb
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 25, 2024
Interneurons
(INs)
in
the
mouse
olfactory
bulb
(OB)
develop
during
an
extensive
period
of
time
that
begins
embryo
and
continues
throughout
lifetime
individual.
The
connectivity
location
these
neurons
is
profoundly
affected
by
generation,
making
developmental
windows
critical
to
understand
circuitry
OB.
Here,
we
focus
on
OB
embryonic
generated
interneurons
(or
EGINs),
which
have
generally
received
less
attention
than
those
adult.
Birthdates
EGINs
were
differentiated
injections
thymidine
analogs
their
final
destinations
phenotypes
analyzed
immunohistochemistry.
We
found
retained
adult
distributed
across
all
layers
However,
a
lateral-to-medial
neurogenic
gradient
seen
only
earliest
EGINs.
Within
granule
cell
layer
(GCL),
predominantly
accumulated
superficial
region
at
almost
ages
remained
there
adulthood.
Immunostaining
for
calbindin,
parvalbumin,
tyrosine
hydroxylase,
calretinin
largely
negative
suggesting
may
represent
subpopulations
INs
are
not
yet
fully
characterized.
Using
utero
electroporation
label
EGIN
progenitors,
demonstrated
they
reach
primordial
as
early
E13
begin
differentiate
apical
dendrites
E15.
At
E16,
progenitors
clustered
into
chain
migrating
neuroblasts
denoting
rostral
migratory
stream
(RMS).
Collectively,
our
data
highlight
importance
studying
isolated
better
formation
circuits
define
responses.
Language: Английский