bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 21, 2024
Abstract
The
dividing
stem
cells
of
the
developing
brain
are
radial
glial
neural
progenitor
(NPCs),
multifunctional
that
proliferate
to
generate
all
brain,
but
also
act
as
scaffolds
for
their
migrating
neuron
progeny,
guideposts
pathfinding
growing
axons
and
regulators
synaptic
activity.
These
remarkable
perform
these
very
different
activities
while
remaining
in
contact
with
inner
outer
surface
ever-growing
brain.
NPCs
synthesize
proteins
locally
support
compartmentalized
protein
expression
required
specialized
functions,
it
is
not
clear
how
necessary
processing
normally
occurs
Golgi
apparatus
achieved
at
locations
far
from
cell
body.
satellites,
motile
organelles
members
maturation
machinery,
control
glycosylation
polarized
like
neurons.
To
investigate
whether
rely
on
we
expressed
a
fluorescent
reporter
label
satellites
intact
brains
Xenopus
laevis
tadpoles.
Quantitative
analysis
vivo
timelapse
images
revealed
dynamic,
distribute
throughout
cell,
suggesting
have
local
proteostasis
diverse
functions.
iScience,
Journal Year:
2024,
Volume and Issue:
27(4), P. 109342 - 109342
Published: Feb. 27, 2024
The
existence
of
neural
stem
cells
(NSCs)
in
adult
human
brain
neurogenic
regions
remains
unresolved.
To
address
this,
we
created
a
cell
atlas
the
subventricular
zone
(SVZ)
derived
from
fresh
neurosurgical
samples
using
single-cell
transcriptomics.
We
discovered
2
radial
glia
(RG)-like
populations,
aRG1
and
aRG2.
shared
features
with
fetal
early
RG
(eRG)
aRG2
were
transcriptomically
similar
to
outer
(oRG).
also
captured
neuronal
oligodendrocytic
NSC
states.
found
that
biological
programs
driven
by
their
transcriptomes
support
roles
as
lineage
NSCs.
Finally,
show
these
NSCs
have
potential
transition
between
states
along
trajectories.
These
data
reveal
multipotent
reside
SVZ.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: April 23, 2024
Thyroid
hormones
(TH)
play
critical
roles
during
nervous
system
development
and
patients
carrying
coding
variants
of
MCT8
(monocarboxylate
transporter
8)
or
THRA
(thyroid
hormone
receptor
alpha)
present
a
spectrum
neurological
phenotypes
resulting
from
perturbed
local
TH
action
early
brain
development.
Recently,
human
cerebral
organoids
(hCOs)
emerged
as
powerful
in
vitro
tools
for
disease
modelling
recapitulating
key
aspects
cortex
To
begin
exploring
prospects
this
model
thyroid
research,
we
performed
detailed
characterization
the
spatiotemporal
expression
developing
hCOs.
Immunostaining
showed
membrane
neuronal
progenitor
cell
types
including
neuroepithelial
cells,
radial
glia
cells
(RGCs),
intermediate
progenitors
outer
RGCs.
In
addition,
detected
robust
protein
deep
layer
upper
neurons.
Spatiotemporal
SLC16A2
mRNA
expression,
by
fluorescent
situ
hybridization
(FISH),
was
highly
concordant
with
across
cortical
layers.
FISH
already
neuroepithelium
before
onset
neurogenesis.
remained
low
ventricular
zone,
increased
subventricular
zone
whereas
strong
observed
excitatory
combination
up-regulation
known
T3
response
genes
following
treatment,
these
observations
show
that
hCOs
provide
promising
experimentally
tractable
to
probe
neurogenesis
eventually
consequences
impaired
function
Neurobiology of Disease,
Journal Year:
2024,
Volume and Issue:
199, P. 106550 - 106550
Published: June 6, 2024
Bioenergetics
describe
the
biochemical
processes
responsible
for
energy
supply
in
organisms.
When
these
changes
become
dysregulated
brain
development,
multiple
neurodevelopmental
diseases
can
occur,
implicating
bioenergetics
as
key
regulators
of
neural
development.
Historically,
discovery
disease
affecting
individual
stages
development
has
revealed
critical
roles
that
play
generating
nervous
system.
Bioenergetic-dependent
disorders
include
tube
closure
defects,
microcephaly,
intellectual
disability,
autism
spectrum
disorders,
epilepsy,
mTORopathies,
and
oncogenic
processes.
Developmental
timing
cell-type
specificity
determine
long-term
effects
bioenergetic
mechanisms
on
form
function.
Here,
we
discuss
metabolic
progenitor
specification,
neuronal
differentiation
(neurogenesis),
gliogenesis.
In
general,
transitions
between
glycolysis
oxidative
phosphorylation
are
regulated
early
oncogenesis,
reactive
oxygen
species
(ROS)
mitochondrial
maturity
later
differentiation.
We
also
how
interface
with
developmental
regulation
other
elements,
including
cerebrospinal
fluid
environment.
While
questions
remain
about
interplay
this
review
integrates
current
state
known
intersections
health
disease.
Annual Review of Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
40(1), P. 427 - 452
Published: Oct. 2, 2024
“What
makes
us
human?”
is
a
central
question
of
many
research
fields,
notably
anthropology.
In
this
review,
we
focus
on
the
development
human
neocortex,
part
brain
with
key
role
in
cognition,
to
gain
neurobiological
insight
toward
answering
question.
We
first
discuss
cortical
stem
and
progenitor
cells
human-specific
genes
that
affect
their
behavior.
thus
aim
understand
molecular
foundation
expansion
neocortex
occurred
course
evolution,
as
generally
thought
provide
basis
for
our
unique
cognitive
abilities.
then
review
emerging
evidence
pointing
differences
between
present-day
humans
Neanderthals,
closest
relatives.
Finally,
have
been
implicated
neuronal
circuitry
offer
perspective
future
studies
addressing
what
human.
Trends in Neurosciences,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 1, 2025
The
human
brain
is
characterized
by
impressive
cognitive
abilities.
neocortex
the
seat
of
higher
cognition,
and
expansion
a
hallmark
evolution.
While
developmental
programs
are
similar
in
different
species,
timing
transitions
capacity
neural
progenitor
cells
(NPCs)
to
proliferate
differ,
contributing
increased
production
neurons
during
cortical
development.
Here,
we
review
epigenetic
regulation
corticogenesis,
focusing
mostly
on
humans
while
building
knowledge
from
studies
mice.
We
discuss
metabolic-epigenetic
interplay
as
potential
mechanism
integrate
extracellular
signals
into
chromatin.
Moreover,
synthesize
current
understanding
how
metabolic
deregulation
can
cause
neurodevelopmental
disorders.
Finally,
outline
be
investigated
using
organoid
models.
Bioengineering,
Journal Year:
2022,
Volume and Issue:
9(11), P. 717 - 717
Published: Nov. 20, 2022
Stroke
is
the
second
cause
of
disability
worldwide
as
it
expected
to
increase
its
incidence
and
prevalence.
Despite
efforts
number
patients
eligible
for
recanalization
therapies,
a
significant
proportion
stroke
survivors
remain
permanently
disabled.
This
outcome
boosted
search
efficient
neurorestorative
methods.
Stem
cells
act
through
multiple
pathways:
cell
replacement,
secretion
growth
factors,
promoting
endogenous
reparative
pathways,
angiogenesis,
modulation
neuroinflammation.
Although
neural
stem
are
difficult
obtain,
pose
series
ethical
issues,
require
intracerebral
delivery,
mesenchymal
less
immunogenic,
easy
can
be
transplanted
via
intravenous,
intra-arterial,
or
intranasal
routes.
Extracellular
vesicles
exosomes
have
similar
actions
easier
also
allowing
engineering
deliver
specific
molecules
RNAs
promote
desired
effects.
Appropriate
timing,
dosing,
delivery
protocols
must
established,
possibility
tumorigenesis
settled.
Nonetheless,
cell-
cell-based
therapies
already
entered
clinical
trials.
safe,
evidence
efficacy
impressive
so
far.
Hopefully,
STEP
guidelines
SPAN
program
will
improve
success
rate.
As
such,
therapy
ischemic
holds
great
promise.