Journal of the Association for Research in Otolaryngology,
Год журнала:
2024,
Номер
25(1), С. 5 - 11
Опубликована: Фев. 9, 2024
Abstract
Inner
ear
organoids
derived
from
differentiation
of
human
pluripotent
stem
cells
have
recently
gained
momentum
as
tools
to
study
inner
development
and
developmental
defects.
An
additional
exciting
aspect
about
this
technology
is
represented
by
its
translational
potential,
specifically,
the
use
validate
therapeutics
for
hearing
balance
restoration
on
human/patient-specific
cells.
This
latter
will
be
briefly
discussed
here
including
opportunities
current
limitations.
Signal Transduction and Targeted Therapy,
Год журнала:
2024,
Номер
9(1)
Опубликована: Апрель 26, 2024
The
induced
pluripotent
stem
cell
(iPSC)
technology
has
transformed
in
vitro
research
and
holds
great
promise
to
advance
regenerative
medicine.
iPSCs
have
the
capacity
for
an
almost
unlimited
expansion,
are
amenable
genetic
engineering,
can
be
differentiated
into
most
somatic
types.
been
widely
applied
model
human
development
diseases,
perform
drug
screening,
develop
therapies.
In
this
review,
we
outline
key
developments
iPSC
field
highlight
immense
versatility
of
modeling
therapeutic
applications.
We
begin
by
discussing
pivotal
discoveries
that
revealed
potential
a
nucleus
reprogramming
led
successful
generation
iPSCs.
consider
molecular
mechanisms
dynamics
as
well
numerous
methods
available
induce
pluripotency.
Subsequently,
discuss
various
iPSC-based
cellular
models,
from
mono-cultures
single
type
complex
three-dimensional
organoids,
how
these
models
elucidate
diseases.
use
examples
neurological
disorders,
coronavirus
disease
2019
(COVID-19),
cancer
diversity
disease-specific
phenotypes
modeled
using
iPSC-derived
cells.
also
used
high-throughput
screening
toxicity
studies.
Finally,
process
developing
autologous
allogeneic
therapies
their
alleviate
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Янв. 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.
Molecular Psychiatry,
Год журнала:
2023,
Номер
28(12), С. 5077 - 5089
Опубликована: Март 6, 2023
Abstract
Maternal
immune
activation
(MIA)
during
critical
windows
of
gestation
is
correlated
with
long-term
neurodevelopmental
deficits
in
the
offspring,
including
increased
risk
for
autism
spectrum
disorder
(ASD)
humans.
Interleukin
6
(IL-6)
derived
from
gestational
parent
one
major
molecular
mediators
by
which
MIA
alters
developing
brain.
In
this
study,
we
establish
a
human
three-dimensional
(3D)
vitro
model
treating
induced
pluripotent
stem
cell-derived
dorsal
forebrain
organoids
constitutively
active
form
IL-6,
Hyper-IL-6.
We
validate
our
showing
that
express
machinery
necessary
responding
to
Hyper-IL-6
and
activate
STAT
signaling
upon
treatment.
RNA
sequencing
analysis
reveals
upregulation
histocompatibility
complex
class
I
(MHCI)
genes
response
exposure,
have
been
implicated
ASD.
find
small
increase
proportion
radial
glia
cells
after
treatment
through
immunohistochemistry
single-cell
RNA-sequencing.
further
show
are
cell
type
highest
number
differentially
expressed
genes,
leads
downregulation
related
protein
translation
line
mouse
MIA.
Additionally,
identify
not
found
models
MIA,
might
drive
species-specific
responses
Finally,
abnormal
cortical
layering
as
consequence
summary,
3D
can
be
used
study
cellular
mechanisms
underlying
disorders
such
Bioengineering & Translational Medicine,
Год журнала:
2023,
Номер
8(5)
Опубликована: Июнь 7, 2023
Malignant
tumors
are
one
of
the
leading
causes
death
which
impose
an
increasingly
heavy
burden
on
all
countries.
Therefore,
establishment
research
models
that
closely
resemble
original
tumor
characteristics
is
crucial
to
further
understanding
mechanisms
malignant
development,
developing
safer
and
more
effective
drugs,
formulating
personalized
treatment
plans.
Recently,
organoids
have
been
widely
used
in
owing
their
advantages
including
preserving
structure,
heterogeneity,
cellular
functions
tumor,
together
with
ease
manipulation.
This
review
describes
history
synergistic
combination
three-dimensional
(3D)
culture
approaches
for
emerging
technologies,
tissue-engineered
cell
scaffolds,
microfluidic
devices,
3D
bioprinting,
rotating
wall
vessels,
clustered
regularly
interspaced
short
palindromic
repeats-CRISPR-associated
protein
9
(CRISPR-Cas9).
Additionally,
progress
applications
basic
clinical
organoid
summarized.
includes
studies
mechanism
drug
development
screening,
precision
medicine,
immunotherapy,
simulation
microenvironment.
Finally,
existing
shortcomings
possible
future
directions
discussed.
The
establishment
and
maintenance
of
apical-basal
polarity
is
a
fundamental
step
in
brain
development,
instructing
the
organization
neural
progenitor
cells
(NPCs)
developing
cerebral
cortex.
Particularly,
basally
located
extracellular
matrix
(ECM)
crucial
for
this
process.
In
vitro,
epithelial
polarization
can
be
achieved
via
endogenous
ECM
production,
or
exogenous
supplementation.
While
neuroepithelial
development
recapitulated
organoids,
effects
different
sources
tissue
morphogenesis
remain
underexplored.
Here,
we
show
that
exposure
to
solubilized
basement
membrane
substrate,
Matrigel,
at
early
stages
causes
rapid
rearrangement
architecture.
cultures
exposed
pure
components
unexposed
any
ECM,
acquisition
slower
driven
by
production.
After
onset
neurogenesis,
architecture
neuronal
differentiation
are
largely
independent
initial
source,
but
Matrigel
has
long-lasting
on
patterning.
These
results
advance
knowledge
mechanisms
exogenously
endogenously
guided
morphogenesis,
demonstrating
self-sustainability
processes.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Окт. 25, 2023
Intestinal
organoid
transplantation
is
a
promising
therapy
for
the
treatment
of
mucosal
injury.
However,
how
transplanted
organoids
regulate
immune
microenvironment
recipient
mice
and
their
role
in
treating
intestinal
ischemia-reperfusion
(I/R)
injury
remains
unclear.
Here,
we
establish
method
transplanting
into
I/R
mice.
We
find
that
improve
mouse
survival,
promote
self-renewal
stem
cells
after
I/R,
depending
on
enhanced
ability
macrophages
polarized
to
an
anti-inflammatory
M2
phenotype.
Specifically,
report
L-Malic
acid
(MA)
highly
expressed
enriched
organoids-derived
conditioned
medium
cecal
contents
mice,
demonstrating
secrete
MA
during
engraftment.
Both
vivo
vitro
experiments
demonstrate
induces
macrophage
polarization
restores
interleukin-10
levels
SOCS2-dependent
manner.
This
study
provides
therapeutic
strategy
ABSTRACT
Recent
years
have
seen
exciting
progress
across
human
embryo
research,
including
new
methods
for
culturing
embryos,
transcriptional
profiling
of
embryogenesis
and
gastrulation,
mapping
lineage
trajectories,
experimenting
on
stem
cell-based
models.
These
advances
are
beginning
to
define
the
dynamical
principles
development
stages,
tissues
organs,
enabling
a
better
understanding
before
birth
in
health
disease,
potentially
leading
improved
treatments
infertility
developmental
disorders.
However,
there
still
significant
roadblocks
en
route
this
goal.
Here,
we
highlight
technical
challenges
studying
early
propose
ways
means
overcome
some
these
constraints.
Journal of Controlled Release,
Год журнала:
2024,
Номер
372, С. 751 - 777
Опубликована: Июль 4, 2024
Despite
significant
advances,
cancer
remains
a
leading
global
cause
of
death.
Current
therapies
often
fail
due
to
incomplete
tumor
removal
and
nonspecific
targeting,
spurring
interest
in
alternative
treatments.
Hyperthermia,
which
uses
elevated
temperatures
kill
cells
or
boost
their
sensitivity
radio/chemotherapy,
has
emerged
as
promising
alternative.
Recent
advancements
employ
nanoparticles
(NPs)
heat
mediators
for
selective
cell
destruction,
minimizing
damage
healthy
tissues.
This
approach,
known
NP
hyperthermia,
falls
into
two
categories:
photothermal
(PTT)
magnetothermal
(MTT).
PTT
utilizes
NPs
that
convert
light
heat,
while
MTT
magnetic
activated
by
alternating
fields
(AMF),
both
achieving
localized
damage.
These
methods
offer
advantages
like
precise
minimal
invasiveness,
reduced
systemic
toxicity.
However,
the
efficacy
hyperthermia
depends
on
many
factors,
particular,
properties,
microenvironment
(TME),
TME-NP
interactions.
Optimizing
this
treatment
requires
accurate
monitoring
strategies,
such
nanothermometry
biologically
relevant
screening
models
can
better
mimic
physiological
features
human
body.
review
explores
state-of-the-art
NP-mediated
discussing
available
nanomaterials,
strengths
weaknesses,
characterization
methods,
future
directions.
Our
particular
focus
lies
preclinical
techniques,
providing
an
updated
perspective
relevance
journey
towards
clinical
trials.