Successful
neurogenesis
requires
adequate
proliferation
of
neural
stem
cells
(NSCs)
and
their
progeny,
followed
by
neuronal
differentiation,
maturation
survival.
NSCs
inhabit
a
complex
cellular
microenvironment,
the
niche,
which
influences
behaviour.
To
ensure
sustained
neurogenesis,
niche
must
respond
to
extrinsic,
environmental
changes
whilst
fulfilling
intrinsic
requirements
neurogenic
program
adapting
roles
accordingly.
However,
very
little
is
known
about
how
different
adjust
properties
such
inputs.
Here,
we
show
that
nutritional
NSC-derived
signals
induce
remodelling
Drosophila
cortex
glia,
this
glial
evolving
needs
NSCs.
First,
nutrition-induced
activation
PI3K/Akt
drives
glia
expand
membrane
processes.
Second,
when
emerge
from
quiescence
resume
proliferation,
they
signal
promote
formation
bespoke
structure
around
each
NSC
lineage.
The
remodelled
essential
for
newborn
neuron
Science,
Journal Year:
2018,
Volume and Issue:
360(6384), P. 99 - 102
Published: April 5, 2018
Staging
quiescent
cells
Tissue-specific
stem
either
divide
or
wait
in
a
state
until
needed
by
the
body.
Quiescent
have
been
thought
to
reside
G
0
stage
before
activating
reenter
cell
cycle.
However,
Otsuki
and
Brand
now
show
that
most
Drosophila
brain
are
arrested
2
.
Cells
two
phases
display
differences;
for
example,
awaken
more
quickly
than
cells,
with
conserved
pseudokinase
Tribbles
playing
regulatory
role.
Elucidating
different
pathways
mechanisms
underlying
quiescence
could
help
inform
regenerative
drug
design.
Science
,
this
issue
p.
99
Frontiers in Neuroscience,
Journal Year:
2014,
Volume and Issue:
8
Published: Nov. 7, 2014
Central
nervous
system
(CNS)
function
is
dependent
on
the
stringent
regulation
of
metabolites,
drugs,
cells,
and
pathogens
exposed
to
CNS
space.
Cellular
blood-brain
barrier
(BBB)
structures
are
highly
specific
checkpoints
governing
entry
exit
all
small
molecules
from
brain
interstitial
space,
but
precise
mechanisms
that
regulate
BBB
not
well
understood.
In
addition,
has
long
been
a
challenging
obstacle
pharmacologic
treatment
diseases;
thus
model
systems
can
parse
functions
desirable.
this
study,
we
sought
define
transcriptome
adult
Drosophila
melanogaster
by
isolating
surface
glia
with
fluorescence
activated
cell
sorting
(FACS)
profiling
their
gene
expression
microarrays.
By
comparing
these
glia,
neurons,
whole
brains,
present
catalog
transcripts
selectively
enriched
at
BBB.
We
found
fly
show
high
many
ATP-binding
cassette
(ABC)
solute
carrier
(SLC)
transporters,
adhesion
molecules,
metabolic
enzymes,
signaling
components
xenobiotic
metabolism
pathways.
Using
sequence-based
alignments,
compare
Murine
transcriptomes
discover
shared
chemoprotective
molecule
control
pathways,
affirming
relevance
invertebrate
models
for
studying
evolutionary
conserved
properties.
The
valuable
vertebrate
insect
biologists
alike
as
resource
proteins
underlying
diffusion
development
maintenance,
glial
biology,
drug
transport
tissue
barriers.
Cell
diversity
of
the
brain
and
how
it
is
affected
by
starvation,
remains
largely
unknown.
Here,
we
introduce
a
single
cell
transcriptome
atlas
entire
Drosophila
first
instar
larval
brain.
We
assigned
cell-type
identity
based
on
known
marker
genes,
distinguishing
five
major
groups:
neural
progenitors,
differentiated
neurons,
glia,
undifferentiated
neurons
non-neural
cells.
All
classes
were
further
subdivided
into
multiple
subtypes,
revealing
biological
features
various
cell-types.
assessed
transcriptional
changes
in
response
to
starvation
at
single-cell
level.
While
after
composition
unaffected,
profile
several
clusters
changed.
Intriguingly,
different
cell-types
show
very
distinct
responses
suggesting
presence
cell-specific
programs
for
nutrition
availability.
Establishing
provides
powerful
tool
explore
assess
genetic
profiles
from
developmental,
functional
behavioral
perspectives.
Cold Spring Harbor Perspectives in Biology,
Journal Year:
2015,
Volume and Issue:
unknown, P. a019117 - a019117
Published: Aug. 10, 2015
Laura
Boulan1,2,3,
Marco
Milán4
and
Pierre
Léopold1,2,3
1University
of
Nice-Sophia
Antipolis,
06108
Nice,
France
2CNRS,
University
3INSERM,
45ICREA,
Parc
Cientific
de
Barcelona,
08028
Spain
Correspondence:
laura.boulan{at}unice.fr;
leopold{at}unice.fr
Frontiers in Neuroscience,
Journal Year:
2014,
Volume and Issue:
8
Published: Dec. 16, 2014
The
invertebrate
blood-brain
barrier
field
is
growing
at
a
rapid
pace
and,
in
recent
years,
studies
have
shown
physiologic
and
molecular
complexity
that
has
begun
to
rival
its
vertebrate
counterpart.
Novel
mechanisms
of
paracellular
maintenance
through
GPCR
signaling
were
the
first
demonstrations
complex
adaptive
physiology.
Building
upon
this
work,
integrity
recently
been
require
coordinated
function
all
layers
compound
structure,
analogous
between
neurovascular
unit.
These
findings
strengthen
notion
many
are
conserved
vertebrates
invertebrates,
suggest
novel
model
organisms
will
significant
impact
on
understanding
BBB
functions.
In
vein,
important
roles
coordinating
localized
systemic
dictate
organism
development
growth
beginning
show
how
can
govern
whole
animal
physiologies.
This
includes
functions
gap
junctions
orchestrating
synchronized
neuroblast
proliferation,
secreted
antagonists
insulin
receptor
signaling.
advancements
others
pushing
forward
exciting
new
directions.
review,
we
provide
synopsis
anatomy
physiology,
with
focus
insights
from
past
5
highlight
areas
for
future
study.
Developmental Neurobiology,
Journal Year:
2020,
Volume and Issue:
81(5), P. 438 - 452
Published: Feb. 25, 2020
Abstract
Animals
are
able
to
move
and
react
in
manifold
ways
external
stimuli.
Thus,
environmental
stimuli
need
be
detected,
information
must
processed,
and,
finally,
an
output
decision
transmitted
the
musculature
get
animal
moving.
All
these
processes
depend
on
nervous
system
which
comprises
intricate
neuronal
network
many
glial
cells.
Glial
cells
have
equally
important
contribution
function
as
their
counterpart.
Manifold
roles
attributed
glia
ranging
from
controlling
cell
number
axonal
pathfinding
regulation
of
synapse
formation,
function,
plasticity.
metabolically
support
neurons
contribute
blood–brain
barrier.
aforementioned
aspects
require
extensive
cell–cell
interactions
between
Not
surprisingly,
found
all
phyla
executed
by
evolutionarily
conserved
molecules.
Here,
we
review
recent
advance
understanding
neuron–glia
interaction
Drosophila
melanogaster
suggest
that
work
simple
model
organisms
will
shed
light
mammalian
cells,
too.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(12), P. 2658 - 2658
Published: Nov. 23, 2023
Brain
cancers
and
neurodegenerative
diseases
are
on
the
rise,
treatments
for
central
nervous
system
(CNS)
remain
limited.
Despite
significant
advancement
in
drug
development
technology
with
emerging
biopharmaceuticals
like
gene
therapy
or
recombinant
protein,
clinical
translational
rate
of
such
to
treat
CNS
disease
is
extremely
poor.
The
blood–brain
barrier
(BBB),
which
separates
brain
from
blood
protects
microenvironment
maintain
essential
neuronal
functions,
poses
greatest
challenge
delivery.
Many
strategies
have
been
developed
over
years
include
local
disruption
BBB
via
physical
chemical
methods,
transport
across
transcytosis
by
targeting
some
endogenous
proteins
expressed
brain-capillary.
Drug
delivery
an
ever-evolving
topic,
although
there
were
multiple
review
articles
literature,
update
warranted
due
continued
growth
new
innovations
research
this
topic.
Thus,
attempt
highlight
recent
employed
overcome
challenges
while
emphasizing
necessity
investing
more
efforts
technologies
parallel
development.
Cold Spring Harbor Perspectives in Biology,
Journal Year:
2024,
Volume and Issue:
16(1), P. a041423 - a041423
Published: Jan. 1, 2024
Vilaiwan
M.
Fernandes1,
Vanessa
Auld2
and
Christian
Klämbt3
1Department
of
Cell
Developmental
Biology,
University
College
London,
London
UC1E
6DE,
United
Kingdom
2Department
Zoology,
British
Columbia,
Vancouver,
Columbia
V6T
1Z4,
Canada
3Institute
for
Neuro-
Behavioral
Münster,
Münster
48149,
Germany
Correspondence:
klaembt{at}uni-muenster.de
Frontiers in Aging Neuroscience,
Journal Year:
2024,
Volume and Issue:
16
Published: Feb. 19, 2024
Introduction
The
goal
of
this
study
is
to
explore
the
pharmacological
potential
amyloid-reducing
vasodilator
fasudil,
a
selective
Ras
homolog
(Rho)-associated
kinases
(ROCK)
inhibitor,
in
P301S
tau
transgenic
mouse
model
(Line
PS19)
neurodegenerative
tauopathy
and
Alzheimer's
disease
(AD).
Methods
We
used
LC-MS/MS,
ELISA
bioinformatic
approaches
investigate
effect
treatment
with
fasudil
on
brain
proteomic
profile
PS19
mice.
also
explored
efficacy
reducing
phosphorylation,
beneficial
and/or
toxic
effects
its
administration
Results
Proteomic
profiling
mice
brains
exposed
revealed
activation
mitochondrial
tricarboxylic
acid
(TCA)
cycle
blood-brain
barrier
(BBB)
gap
junction
metabolic
pathways.
observed
significant
negative
correlation
between
levels
phosphorylated
(pTau)
at
residue
396
both
metabolite
hydroxyfasudil.
Conclusions
Our
results
provide
evidence
proteins
pathways
related
mitochondria
BBB
functions
by
support
further
development
therapeutic
for
AD.