IEEE Reviews in Biomedical Engineering,
Год журнала:
2024,
Номер
18, С. 211 - 230
Опубликована: Дек. 9, 2024
Cardiac
organoids
represent
an
important
bioengineering
opportunity
in
the
development
of
models
to
study
human
heart
pathophysiology.
By
incorporating
multiple
cardiac
cell
types
three-dimensional
culture
and
developmentally-guided
biochemical
signaling,
recapitulate
numerous
features
tissue.
However,
tissue
also
experiences
a
variety
mechanical
forces
as
develops
over
course
each
contraction
cycle.
It
is
now
clear
that
these
impact
cellular
specification,
phenotype,
function,
should
be
incorporated
into
engineering
order
generate
better
models.
In
this
review,
we
discuss
strategies
for
report
effects
organoid
design
on
function
cells.
We
then
environment
heart,
including
arising
from
elasticity,
contraction,
blood
flow,
stretch,
efforts
mimic
biophysical
cues
organoids.
Finally,
review
emerging
areas
research,
development,
formation
multi-organ
models,
simulation
spaceflight
consider
how
investigations
might
benefit
inclusion
cues.
Materials Today Bio,
Год журнала:
2025,
Номер
unknown, С. 101728 - 101728
Опубликована: Апрель 1, 2025
Osteoarthritis
(OA)
is
a
musculoskeletal
degenerative
disease
characterized
by
alterations
in
cartilage
and
subchondral
bone
leading
to
impaired
joint
function.
OA
disproportionally
affects
females
more
than
males,
yet
the
molecular
mechanisms
underlying
these
biological
sex
differences
remain
elusive.
Current
therapeutic
strategies
halt
progression
of
are
still
lacking,
part
due
limited
predictive
potential
standard
models
which
often
do
not
account
for
disparities.
Herein,
an
organ-on-chip
microfluidic
platform
was
developed
model
osteochondral
unit,
composed
adjacent
culture
chambers,
capture
sex-specific
hallmarks
OA.
Sex-stratified
human
primary
chondrocytes
osteoblasts
were
compartmentalized
within
biomimetic
hydrogels
emulating
bone-cartilage
interface,
subjected
inflammatory
triggers
mimic
onset
We
confirmed
that
interleukin-1β
Tumor
Necrosis
Factor-α
stimulation
triggered
upregulation
pro-inflammatory
cytokines
matrix
metalloproteinases
related
genes
all
donors,
with
marginal
trends
increased
expression
female
cells.
In
addition,
metabolic
labeling
coupled
confocal
imaging
revealed
modulated
extracellular
deposition
fashion.
Not
only
but
also
remodeling
altered
upon
inflammation,
significant
reduction
stiffness
both
compartments.
Overall,
sex-stratified
unit
on-chips
offer
novel
insights
into
cellular
responses
insults,
demonstrating
importance
incorporating
stratification
emergent
models.
Thus,
this
provides
physiologically
relevant
3D
microenvironment
further
investigate
drivers
OA,
paving
way
targeted
therapies.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(4), С. 2124 - 2124
Опубликована: Фев. 9, 2024
The
human
retina
is
a
complex
anatomical
structure
that
has
no
regenerative
capacity.
pathogenesis
of
most
retinopathies
can
be
attributed
to
inflammation,
with
the
activation
inflammasome
protein
platform,
and
impact
oxidative
stress
on
regulation
apoptosis
autophagy/mitophagy
in
retinal
cells.
In
recent
years,
new
therapeutic
approaches
treat
have
been
investigated.
Experimental
data
suggest
secretome
mesenchymal
cells
could
reduce
stress,
autophagy,
cells,
turn,
latter
induce
changes
Other
studies
evidenced
noncoding
(nc)RNAs
might
targets
for
retinopathy
treatment
novel
disease
biomarkers
since
correlation
found
between
ncRNA
levels
retinopathies.
A
field
explore
interaction
observed
ocular
intestinal
microbiota;
indeed,
findings
shown
alteration
gut
microbiota
seems
linked
diseases,
suggesting
gut-eye
axis.
To
therapeutical
strategies
retinopathies,
it
important
use
proper
models
mimic
complexity
retina.
this
context,
organoids
represent
good
model
study
pathophysiology
Advanced Intelligent Systems,
Год журнала:
2024,
Номер
6(9)
Опубликована: Июнь 19, 2024
Studying
the
behavior
of
electroactive
cells,
such
as
firing
dynamics
and
chemical
secretion,
is
crucial
for
developing
human
disease
models
therapeutics.
Following
recent
advances
in
cell
culture
technology,
traditional
monolayers
are
optimized
to
resemble
more
3D,
organ‐like
structures.
The
biological
electrochemical
complexity
these
structures
requires
devices
with
adaptive
shapes
novel
features,
precise
electrophysiological
mapping
stimulation
case
brain‐
heart‐derived
tissues.
However,
conventional
organ‐on‐chip
platforms
often
fall
short,
they
do
not
recreate
native
environment
cells
lack
functional
interfaces
necessary
long‐term
monitoring.
Origami‐on‐a‐chip
offer
a
solution
this
problem,
can
flexibly
adapt
structure
desired
sample
be
integrated
components
enabled
by
chosen
materials.
In
review,
evolution
origami‐on‐a‐chip
biointerfaces
discussed,
emphasizing
folding
stimuli,
materials,
critical
findings.
prospects,
microfluidic
integration,
tissue
engineering
scaffolds,
multi‐organoid
networks
included,
allowing
patient‐specific
diagnoses
therapies
through
computational
vitro
modeling.
Biology of Sex Differences,
Год журнала:
2024,
Номер
15(1)
Опубликована: Дек. 2, 2024
Abstract
In
vitro
models
serve
as
indispensable
tools
for
advancing
our
understanding
of
biological
processes,
elucidating
disease
mechanisms,
and
establishing
screening
platforms
drug
discovery.
Kidneys
play
an
instrumental
role
in
the
transport
elimination
drugs
toxins.
Nevertheless,
despite
well-documented
inter-individual
variability
kidney
function
multifaceted
nature
renal
diseases—spanning
from
their
origin,
trigger
which
segment
is
affected—to
presentation,
progression
prognosis,
few
studies
take
into
consideration
variable
sex.
Notably,
inherent
disparities
between
female
male
biology
warrants
a
more
comprehensive
representation
within
kidney.
The
omission
sex
fundamental
carries
substantial
risk
overlooking
sex-specific
mechanisms
implicated
health
disease,
along
with
potential
differences
responsiveness
toxicity
profiles
sexes.
This
review
emphasizes
importance
incorporating
cellular,
functional
features
activity
models.
For
that,
we
thoroughly
document
propose
strategic
experimental
framework
to
integrate
sex-based
human
by
outlining
critical
design
criteria
elucidate
at
cellular
tissue
levels.
goal
enhance
accuracy
unravel
improve
impact
on
efficacy
safety
profiles,
paving
way
patient-specific
treatment
modalities.
Cardiomyocytes
in
the
adult
human
heart
are
quiescent
and
those
lost
following
injury
not
replaced
by
proliferating
survivors.
Considerable
effort
has
been
made
to
understand
mechanisms
underlying
cardiomyocyte
cell
cycle
exit
re-entry,
with
view
discovering
therapeutics
that
could
stimulate
proliferation
regeneration.
The
advent
of
large
compound
libraries
robotic
liquid
handling
platforms
enabled
screening
thousands
conditions
a
single
experiment
but
success
these
screens
depends
on
appropriateness
quality
model
used.
Quantification
(human)
high
throughput
remained
problematic
because
conventional
antibody-based
staining
is
costly,
technically
challenging
does
discriminate
between
division
failure
karyokinesis
or
cytokinesis.
Live
imaging
provided
alternatives
facilitate
high-throughput
have
other
limitations.
Here,
we
(i)
review
features
cardiomyocytes,
(ii)
discuss
various
fluorescent
reporter
systems,
(iii)
speculate
what
improve
their
predictive
value
context
proliferation.
Finally,
consider
how
new
methods
can
be
used
combination
state-of-the-art
three-dimensional
cardiac
organoid
identify
pro-proliferative
signalling
pathways
regeneration
heart.
IEEE Reviews in Biomedical Engineering,
Год журнала:
2024,
Номер
18, С. 211 - 230
Опубликована: Дек. 9, 2024
Cardiac
organoids
represent
an
important
bioengineering
opportunity
in
the
development
of
models
to
study
human
heart
pathophysiology.
By
incorporating
multiple
cardiac
cell
types
three-dimensional
culture
and
developmentally-guided
biochemical
signaling,
recapitulate
numerous
features
tissue.
However,
tissue
also
experiences
a
variety
mechanical
forces
as
develops
over
course
each
contraction
cycle.
It
is
now
clear
that
these
impact
cellular
specification,
phenotype,
function,
should
be
incorporated
into
engineering
order
generate
better
models.
In
this
review,
we
discuss
strategies
for
report
effects
organoid
design
on
function
cells.
We
then
environment
heart,
including
arising
from
elasticity,
contraction,
blood
flow,
stretch,
efforts
mimic
biophysical
cues
organoids.
Finally,
review
emerging
areas
research,
development,
formation
multi-organ
models,
simulation
spaceflight
consider
how
investigations
might
benefit
inclusion
cues.