BackgroundCardiovascular
diseases
(CVDs)
remain
the
leading
global
cause
of
morbidity
and
mortality,
necessitating
innovative
research
approaches
to
bridge
translational
gap
between
preclinical
clinical
settings.Traditional
models,
such
as
two-dimensional
(2D)
cell
cultures
animal
are
limited
in
replicating
human
cardiac
physiology.Cardiac
organoids,
derived
from
pluripotent
stem
cells,
have
emerged
transformative
tools
cardiovascular
research,
o
ering
3D
models
that
recapitulate
key
structural
functional
features
heart.
ObjectivesThis
study
aims
explore
potential
organoids
disease
modelling,
drug
discovery,
regenerative
medicine
while
addressing
current
limitations
proposing
future
directions
for
their
application.
MethodsA
comprehensive
review
recent
advancements
organoid
was
conducted,
focusing
on
methodologies
generation,
applications
innovations
overcome
technical
biological
limitations.Emphasis
placed
integrating
multi-omics
technologies,
arti
cial
intelligence
(AI),
bioengineering
approaches.
ResultsCardiac
successfully
modelled
various
conditions,
including
myocardial
infarction,
genetic
cardiomyopathies,
congenital
heart
defects.Multi-omics
genomics,
transcriptomics,
proteomics,
elucidated
molecular
mechanisms,
AI-driven
computational
modelling
has
enhanced
data
analysis
predictive
simulations.Despite
promise,
challenges
persist
achieving
vascularization,
cellular
maturity,
scalability,
limiting
translation.
ConclusionsCardiac
er
a
physiologically
relevant
platform
advancing
research.Their
revolutionize
testing,
personalized
medicine,
therapies
underscores
impact.Addressing
through
interdisciplinary
innovations,
vascularized
systems
organoid-on-chip
platforms,
will
enhance
utility.With
continued
advancements,
hold
promise
improving
therapeutic
outcomes
understanding
diseases.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(12), P. 2714 - 2714
Published: Nov. 27, 2024
Cardiovascular
disease
comprises
a
group
of
disorders
affecting
or
originating
within
tissues
and
organs
the
cardiovascular
system;
most,
if
not
all,
will
eventually
result
in
cardiomyocyte
dysfunction
death,
negatively
impacting
cardiac
function.
Effective
models
are
thus
important
for
understanding
crucial
aspects
progression,
while
recent
advancements
stem
cell
biology
have
allowed
use
populations
to
derive
such
models.
These
include
three-dimensional
(3D)
as
cell-based
embryos
(SCME)
well
organoids,
many
which
frequently
derived
from
embryoid
bodies
(EB).
Not
only
can
they
recapitulate
3D
form
function,
but
developmental
programs
governing
self-organization
into
more
complex
well.
Many
different
organoids
SCME
constructs
been
generated
years
recreate
tissue
that
give
rise
its
cellular
composition
unique
morphology.
It
is
purpose
this
narrative
literature
review
describe
summarize
recently
organoid
their
recapitulation
genetic
acquired
disease.
Owing
examined,
focus
on
injury
associated
with
embryonic/fetal
tissues.
Frontiers in Cellular Neuroscience,
Journal Year:
2024,
Volume and Issue:
18
Published: Dec. 18, 2024
Multiple
sclerosis
(MS),
a
debilitating
autoimmune
disorder
targeting
the
central
nervous
system
(CNS),
is
marked
by
relentless
demyelination
and
inflammation.
Clinically,
it
presents
in
three
distinct
forms:
relapsing-remitting
MS
(RRMS),
primary
progressive
(PPMS),
secondary
(SPMS).
While
disease-modifying
therapies
(DMTs)
offer
some
relief
to
people
with
RRMS,
treatment
options
for
(pMS)
remain
frustratingly
inadequate.
This
gap
highlights
an
urgent
need
advanced
disease
modeling
techniques
unravel
intricate
pathology
of
pMS.
Human
induced
pluripotent
stem
cell
(iPSC)
technologies
brain
organoids
are
emerging
as
promising
tools
both
2D
3D
Organoid,
Journal Year:
2024,
Volume and Issue:
4, P. e12 - e12
Published: Dec. 25, 2024
Neurodegenerative
diseases
(NDs)
such
as
Parkinson’s
disease
(PD)
and
Alzheimer’s
(AD)
are
progressive
disorders
characterized
by
complex,
human-specific
pathology
that
poses
challenges
to
drug
discovery
efforts.
Traditional
models,
including
two-dimensional
cell
cultures
animal
often
fall
short
in
replicating
the
intricate
cellular
interactions
observed
human
neurodegeneration.
This
review
explores
potential
of
brain
organoid
technology
address
these
limitations
offer
a
model
more
relevant
humans.
Recent
advancements
induced
pluripotent
stem
(iPSC)
have
enabled
generation
patient-derived
organoids
differentiate
into
various
neural
types
within
3-dimensional
structures.
These
iPSC-derived
establish
physiologically
microenvironment
mimics
architecture
diversity.
synthesizes
studies
on
application
modeling
PD
AD
pathology,
approaches
improve
fidelity.
Brain
replicate
disease-specific
features,
dopaminergic
neuron
degeneration
amyloid
plaque
formation
AD,
offering
valuable
insights
mechanisms
therapeutic
targets.
However,
remain,
incomplete
maturation,
batch
variability,
absence
vascularization
complete
cortical
layering.
Bioengineering
approaches,
CRISPR-based
gene
editing
organ-on-a-chip
technologies,
being
investigated
overcome
obstacles.
presents
transformative
platform
for
study
NDs,
facilitating
detailed
research
testing
therapeutics.
Overcoming
existing
is
crucial
maximizing
translational
value
organoids,
advancing
personalized
medicine,
supporting
development
effective
therapies
NDs.
BackgroundCardiovascular
diseases
(CVDs)
remain
the
leading
global
cause
of
morbidity
and
mortality,
necessitating
innovative
research
approaches
to
bridge
translational
gap
between
preclinical
clinical
settings.Traditional
models,
such
as
two-dimensional
(2D)
cell
cultures
animal
are
limited
in
replicating
human
cardiac
physiology.Cardiac
organoids,
derived
from
pluripotent
stem
cells,
have
emerged
transformative
tools
cardiovascular
research,
o
ering
3D
models
that
recapitulate
key
structural
functional
features
heart.
ObjectivesThis
study
aims
explore
potential
organoids
disease
modelling,
drug
discovery,
regenerative
medicine
while
addressing
current
limitations
proposing
future
directions
for
their
application.
MethodsA
comprehensive
review
recent
advancements
organoid
was
conducted,
focusing
on
methodologies
generation,
applications
innovations
overcome
technical
biological
limitations.Emphasis
placed
integrating
multi-omics
technologies,
arti
cial
intelligence
(AI),
bioengineering
approaches.
ResultsCardiac
successfully
modelled
various
conditions,
including
myocardial
infarction,
genetic
cardiomyopathies,
congenital
heart
defects.Multi-omics
genomics,
transcriptomics,
proteomics,
elucidated
molecular
mechanisms,
AI-driven
computational
modelling
has
enhanced
data
analysis
predictive
simulations.Despite
promise,
challenges
persist
achieving
vascularization,
cellular
maturity,
scalability,
limiting
translation.
ConclusionsCardiac
er
a
physiologically
relevant
platform
advancing
research.Their
revolutionize
testing,
personalized
medicine,
therapies
underscores
impact.Addressing
through
interdisciplinary
innovations,
vascularized
systems
organoid-on-chip
platforms,
will
enhance
utility.With
continued
advancements,
hold
promise
improving
therapeutic
outcomes
understanding
diseases.