Innovative Atherosclerosis Models: Advancing Pathophysiology and Translational Research
Huiting Jiang,
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Yukun Liao,
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Mengliang Zhu
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et al.
Research,
Journal Year:
2025,
Volume and Issue:
8
Published: Jan. 1, 2025
Atherosclerosis
(AS)
is
a
chronic
inflammatory
condition
influenced
by
glucose
and
lipid
disorders,
oxidative
stress,
thrombosis,
reflecting
the
complexity
of
its
pathological
process.
The
development
accurate
experimental
models
that
simulate
human
AS
essential
for
understanding
initiation
progression.
This
review
summarizes
current
research
analyzes
their
specific
application
scenarios.
We
discuss
tissue-engineered
blood
vessels
(TEBVs)
vessels-on-a-chip
(VoCs),
which
leverage
tissue
engineering
precise
microenvironmental
control
to
construct
in
vitro
closely
resemble
structure
function
AS.
Isolated
vessel
segments
from
live
animals
provide
valuable
tool
investigating
due
physiological
similarity,
controllability,
reproducibility.
further
outlines
construction
animal
through
high-fat
diets
gene-editing
techniques,
highlighting
how
immune-inflammatory
responses,
mechanical
arterial
injury,
hemodynamic
changes
accelerate
model
development.
comprehensive
analysis
highlights
potential
revolutionize
theranostic
applications
clinical
translational
research,
paving
way
more
personalized
effective
treatments
near
future.
Language: Английский
Human Vascularized Adipose Tissue Organoids Reveal Endothelial-Adipocyte Interactions at Single-Cell Resolution
Published: Jan. 1, 2025
White
adipose
tissue
(WAT)
is
essential
for
energy
storage
and
metabolic
homeostasis,
plays
a
central
role
in
the
pathology
of
obesity
type
2
diabetes.
Vascular
networks
within
WAT
support
oxygen
nutrient
supply
regulate
adipogenesis,
yet
mechanisms
underlying
endothelial-adipocyte
crosstalk
under
both
healthy
dysfunctional
conditions
remain
unclear.
Here,
we
present
vascularized
organoid
(vAO)
model
engineered
from
human
adipose-derived
stem
cells
induced
pluripotent
cell-derived
endothelial
(SC-ECs).
The
3D
cell
culture
enables
adipogenesis
angiogenesis
controlled
conditions.
vAOs
demonstrated
enhanced
β-adrenergic-induced
lipolysis
insulin-stimulated
glucose
uptake.
Single-cell
transcriptomics
revealed
distinct
stromal
subtypes,
including
perivascular
adipocyte
precursors
maturing
SC-ECs
shaped
by
PDGFB
signaling.
knockdown
disrupted
alignment
lipolysis,
highlighting
critical
endothelial-pericyte
interactions.
This
study
provides
versatile
platform
to
dissect
explore
pathways
that
control
WAT-remodeling
determine
its
function.
Our
vAO
therefore
presents
unique
molecularly
functionally
patient-specific
dysfunctions,
advancing
our
portfolio
personalized
therapies
importance
communication.
Language: Английский
Towards advanced regenerative therapeutics to tackle cardio-cerebrovascular diseases
Xi Chen,
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Weiping Lin,
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Micky D. Tortorella
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et al.
American Heart Journal Plus Cardiology Research and Practice,
Journal Year:
2025,
Volume and Issue:
53, P. 100520 - 100520
Published: March 1, 2025
The
development
of
vascularized
organoids
as
novel
modelling
tools
the
human
cardio-cerebrovascular
system
for
preclinical
research
has
become
an
essential
platform
studying
tissues/organs
personalized
therapeutics
during
recent
decades.
Organ-on-chip
technology
is
promising
investigating
physiological
in
vitro
responses
drug
screening
and
advanced
disease
models.
Vascularized
tissue/organ-on-a-chip
benefits
every
step
discovery
pipeline
a
tool
with
close
genome
relevance
to
investigate
systems
biology.
Simultaneously,
cardio-cerebrovascular-on-chip-integrated
microfluidic
serves
alternative
animal
(patho-)physiological
processes
blood
vessels
embryonic
disease.
Integrated
next-generation
techniques,
such
three-dimensional
bioprinting
both
cells
matrix,
may
enable
organoid-on-chip-based
therapeutics.
Language: Английский
Artery regeneration: Molecules, mechanisms and impact on organ function
Swarnadip Ghosh,
No information about this author
Bhavnesh Bishnoi,
No information about this author
Soumyashree Das
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et al.
Seminars in Cell and Developmental Biology,
Journal Year:
2025,
Volume and Issue:
171, P. 103611 - 103611
Published: May 2, 2025
Language: Английский
Recent Advances and Future Perspectives in Vascular Organoids and Vessel-on-Chip
Gowtham Reddy Cheruku,
No information about this author
Chloe Veronica Wilson,
No information about this author
Suriya Raviendran
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et al.
Organoids,
Journal Year:
2024,
Volume and Issue:
3(3), P. 203 - 246
Published: Sept. 4, 2024
Recent
advancements
in
vascular
organoid
(VO)
and
vessel-on-chip
(VoC)
technologies
have
revolutionized
our
approach
to
studying
human
diseases,
offering
unprecedented
insights
through
more
physiologically
relevant
models.
VOs
generated
from
pluripotent
stem
cells
exhibit
remarkable
self-organization
capabilities,
forming
complex
three-dimensional
structures
that
closely
mimic
blood
vessel
architecture
function,
while
VoCs
are
engineered
with
microfluidic
systems
meticulously
recreate
the
physical
functional
attributes
of
vessels.
These
innovative
constructs
serve
as
powerful
tools
for
investigating
development,
disease
progression,
therapeutic
efficacy.
By
enabling
creation
patient-specific
VoCs,
they
pave
way
personalized
medicine
approaches,
allowing
researchers
delve
into
genetic
variations,
intricate
cellular
interactions,
dynamic
processes
exceptional
resolution.
The
synergy
between
newly
developed
cutting-edge
has
further
amplified
their
potential,
unveiling
novel
mechanisms
underlying
pathologies
identifying
promising
targets.
Herein,
we
summarize
different
types
present
an
extensive
overview
on
generation
applications
VoCs.
We
will
also
highlight
clinical
translational
challenges
future
perspectives
around
Language: Английский
Recent Advances and Future Perspectives in Vascular Organoids and Vessel-on-Chip
Gowtham Reddy Cheruku,
No information about this author
Chloe Veronica Wilson,
No information about this author
Suriya Raviendran
No information about this author
et al.
Published: July 14, 2024
Recent
advancements
in
vascular
organoid
(VO)
and
vessel-on-chip
(VoC)
technologies
have
revolutionized
our
approach
to
studying
cardiovascular
diseases
(CVDs),
offering
unprecedented
insights
through
more
physiologically
relevant
models.
VOs
generated
from
human
pluripotent
stem
cells
exhibit
remarkable
self-organization
capabilities,
forming
complex
three-dimensional
structures
that
closely
mimic
blood
vessel
architecture
function,
while
VoCs
engineered
with
groundbreaking
microfluidic
systems
meticulously
recreate
the
physical
functional
attributes
of
vessels.
These
innovative
constructs
serve
as
powerful
tools
for
investigating
development,
disease
progression,
therapeutic
efficacy.
By
enabling
creation
patient-specific
VoCs,
they
pave
way
personalized
medicine
approaches,
allowing
researchers
delve
into
genetic
variations,
intricate
cellular
interactions,
dynamic
processes
exceptional
resolution.
The
synergy
between
cutting-edge
such
single-cell
sequencing
high-resolution
imaging
has
further
amplified
their
potential,
unveiling
novel
mechanisms
underlying
CVDs
identifying
promising
targets.
Herein,
we
summarize
different
types
present
an
extensive
overview
on
generation
applications
CVDs.
We
will
also
highlight
clinical
translational
challenges
future
perspectives
around
VoCs.
Language: Английский
Protocol to generate a microfluidic vessels-on-chip platform using human pluripotent stem cell-derived endothelial cells
Caroline Remmert,
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Munkhtur Otgonbayar,
No information about this author
Julius Alexander Perschel
No information about this author
et al.
STAR Protocols,
Journal Year:
2024,
Volume and Issue:
5(3), P. 103300 - 103300
Published: Sept. 1, 2024
Here,
we
present
a
protocol
for
producing
microfluidic
vessel-on-chip
platform
using
human
pluripotent
stem
cell-derived
endothelial
cells
(SC-ECs).
We
describe
steps
manufacturing
the
3D-printed
chip,
cell
culturing
to
generate
SC-ECs,
hydrogel
patterning,
and
formation
cultivation
of
barrier-forming
vessels.
then
detail
procedures
retrieval
media
from
open
chip
enable
multi-omics
analysis.
For
complete
details
on
use
execution
this
protocol,
please
refer
Marder
et
al.
Language: Английский