ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Interfacing
artificial
devices
with
the
human
brain
is
central
goal
of
neurotechnology.
Yet,
our
imaginations
are
often
limited
by
currently
available
paradigms
and
technologies.
Suggestions
for
brain-machine
interfaces
have
changed
over
time,
along
technology.
Mechanical
levers
cable
winches
were
used
to
move
parts
during
mechanical
age.
Sophisticated
electronic
wiring
remote
control
arisen
age,
ultimately
leading
plug-and-play
computer
interfaces.
Nonetheless,
brains
so
complex
that
these
visions,
until
recently,
largely
remained
unreachable
dreams.
The
general
problem,
thus
far,
most
technology
mechanically
and/or
electrically
engineered,
whereas
a
living,
dynamic
entity.
As
result,
worlds
difficult
interface
one
another.
Nanotechnology,
which
encompasses
engineered
solid-state
objects
integrated
circuits,
excels
at
small
length
scales
single
few
hundred
nanometers
and,
thus,
matches
sizes
biomolecules,
biomolecular
assemblies,
cells.
Consequently,
we
envision
nanomaterials
nanotools
as
opportunities
in
alternative
ways.
Here,
review
existing
literature
on
use
nanotechnology
look
forward
discussing
perspectives
limitations
based
authors'
expertise
across
range
complementary
disciplines─from
neuroscience,
engineering,
physics,
chemistry
biology
medicine,
science
mathematics,
social
jurisprudence.
We
focus
but
also
include
information
from
related
fields
when
useful
complementary.
Stem Cells,
Journal Year:
2021,
Volume and Issue:
39(8), P. 1017 - 1024
Published: March 31, 2021
Human
brain
organoids
are
three-dimensional
tissues
that
generated
in
vitro
from
pluripotent
stem
cells
and
recapitulate
the
early
development
of
human
brain.
Brain
consist
mainly
neural
lineage
cells,
such
as
stem/precursor
neurons,
astrocytes,
oligodendrocytes.
However,
all
lack
vasculature,
which
plays
indispensable
roles
not
only
homeostasis
but
also
development.
In
addition
to
delivery
oxygen
nutrition,
accumulating
evidence
suggests
vascular
system
regulates
differentiation,
migration,
circuit
formation
during
Therefore,
vascularization
is
great
importance.
Current
trials
vascularize
various
include
adjustment
cultivation
protocols,
introduction
microfluidic
devices,
transplantation
into
immunodeficient
mice.
this
review,
we
summarize
efforts
accomplish
perfusion
organoids,
discuss
these
attempts
a
forward-looking
perspective.
Advanced Materials,
Journal Year:
2021,
Volume and Issue:
33(45)
Published: Sept. 24, 2021
Abstract
Recent
advances
in
3D
cell
culture
technology
have
enabled
scientists
to
generate
stem
derived
organoids
that
recapitulate
the
structural
and
functional
characteristics
of
native
organs.
Current
organoid
technologies
been
striding
toward
identifying
essential
factors
for
controlling
processes
involved
development,
including
physical
cues
biochemical
signaling.
There
is
a
growing
demand
engineering
dynamic
niches
characterized
by
conditions
resemble
vivo
organogenesis
reproducible
reliable
various
applications.
Innovative
biomaterial‐based
advanced
engineering‐based
approaches
incorporated
into
conventional
methods
facilitate
development
research.
The
recent
engineering,
extracellular
matrices
genetic
modulation,
are
comprehensively
summarized
pinpoint
parameters
critical
organ‐specific
patterning.
Moreover,
perspective
trends
developing
tunable
response
exogenous
endogenous
discussed
next‐generation
developmental
studies,
disease
modeling,
therapeutics.
Cell,
Journal Year:
2024,
Volume and Issue:
187(3), P. 712 - 732.e38
Published: Jan. 8, 2024
Human
brain
development
involves
an
orchestrated,
massive
neural
progenitor
expansion
while
a
multi-cellular
tissue
architecture
is
established.
Continuously
expanding
organoids
can
be
grown
directly
from
multiple
somatic
tissues,
yet
to
date,
solely
established
pluripotent
stem
cells.
Here,
we
show
that
healthy
human
fetal
in
vitro
self-organizes
into
(FeBOs),
phenocopying
aspects
of
vivo
cellular
heterogeneity
and
complex
organization.
FeBOs
expanded
over
long
time
periods.
FeBO
growth
requires
maintenance
integrity,
which
ensures
production
tissue-like
extracellular
matrix
(ECM)
niche,
ultimately
endowing
expansion.
lines
derived
different
areas
the
central
nervous
system
(CNS),
including
dorsal
ventral
forebrain,
preserve
their
regional
identity
allow
probe
positional
identity.
Using
CRISPR-Cas9,
showcase
generation
syngeneic
mutant
for
study
cancer.
Taken
together,
constitute
complementary
CNS
organoid
platform.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Jan. 8, 2024
Abstract
Understanding
metabolic
heterogeneity
is
the
key
to
uncovering
underlying
mechanisms
of
metabolic-related
diseases.
Current
imaging
studies
suffer
from
limitations
including
low
resolution
and
specificity,
model
systems
utilized
often
lack
human
relevance.
Here,
we
present
a
single-cell
platform
enable
direct
lipid
metabolism
with
high
specificity
in
various
human-derived
2D
3D
culture
systems.
Through
incorporation
an
azide-tagged
infrared
probe,
selective
detection
newly
synthesized
lipids
cells
tissue
became
possible,
while
simultaneous
fluorescence
enabled
cell-type
identification
complex
tissues.
In
proof-of-concept
experiments,
were
directly
visualized
human-relevant
among
different
cell
types,
mutation
status,
differentiation
stages,
over
time.
We
identified
upregulated
progranulin-knockdown
induced
pluripotent
stem
their
differentiated
microglia
cells.
Furthermore,
observed
that
neurons
brain
organoids
exhibited
significantly
lower
compared
astrocytes.
Nature,
Journal Year:
2024,
Volume and Issue:
635(8039), P. 690 - 698
Published: Nov. 20, 2024
Human
neural
organoids,
generated
from
pluripotent
stem
cells
in
vitro,
are
useful
tools
to
study
human
brain
development,
evolution
and
disease.
However,
it
is
unclear
which
parts
of
the
covered
by
existing
protocols,
has
been
difficult
quantitatively
assess
organoid
variation
fidelity.
Here
we
integrate
36
single-cell
transcriptomic
datasets
spanning
26
protocols
into
one
integrated
cell
atlas
totalling
more
than
1.7
million
cells1–26.
Mapping
developing
references27–30
shows
primary
types
states
that
have
estimates
similarity
between
counterparts
across
protocols.
We
provide
a
programmatic
interface
browse
query
new
datasets,
showcase
power
annotate
evaluate
Finally,
show
can
be
used
as
diverse
control
cohort
compare
models
disease,
identifying
genes
pathways
may
underlie
pathological
mechanisms
with
models.
The
will
fidelity,
characterize
perturbed
diseased
facilitate
protocol
development.
A
integrating
counterparts,
showing
potential
fidelity