The
adult
human
heart
has
evolved
to
become
a
highly
specialized
organ,
whose
continuous
pumping
of
blood
is
critical
for
survival.
However,
its
ability
regenerate
or
self-repair
following
injury
very
limited,
so
consequently
any
event
disease
resulting
in
damage
the
poses
serious
threat
patient.
Moreover,
cardiovascular
diseases
represent
one
most
pressing
healthcare
concerns
nowadays,
as
they
are
leading
cause
death
worldwide,
and
number
cases
only
expected
increase
years.
Despite
great
progress
made
over
years
treat
diseases,
date
there
no
therapy
able
fully
cure
that
been
damaged.
In
consequence,
dire
need
generate
new
strategies
repair
restore
lost
cardiac
function,
well
develop
accurate
modelling
platforms
advance
understanding
progression
assess
effectiveness
drugs.
Since
advent,
tissue
engineering
regenerative
medicine
regarded
promising
candidate
realise
this
enormous
challenge.
Given
interdisciplinary
nature,
scientific
breakthroughs
different
areas
such
cellular
reprogramming,
polymer
chemistry,
additive
manufacturing
technologies
have
resulted
advancement
One
cornerstone
discoveries
was
generation
induced
pluripotent
stem
cells
subsequent
differentiation
phenotypes,
present
Thesis
revolves
around
their
application
patient-specific
models
humanised
engineered
functional
minitissues.
Firstly,
we
reprogrammed
peripheral
mononuclear
from
transthyretin
amyloid
cardiomyopathy
patient,
cell
line
carrying
c.128G>A
(p.Ser43Asn)
mutation
gene.
Experiments
demonstrated
efficacy
safety
approach,
confirming
pluripotency
cells,
presence
disease-causing
mutation,
removal
reprogramming
vectors.
This
line,
which
now
available
repository,
can
be
used
investigate
biology,
molecular
mechanisms
progression;
an
advanced
model
test
novel
therapeutic
strategies.
Secondly,
aimed
minitissues
by
combining
cardiomyocytes
derived
tridimensional
fibrillar
scaffolds
generated
with
technology
melt
electrowriting.
Compared
conventional
two-dimensional
culture,
enhanced
maturation,
significant
conduction
velocity,
connexin
43
expression
cardiac-associated
genes
MYL2,
GJA5
SCN5A,
isoform
ratios
MYH7/MYH6
MYL2/MYL7
after
28
days
culture.
When
investigating
effect
scaffold
fibres
on
found
placed
close
fibre
were
arranged
parallel
it,
but
alignment
progressively
towards
centre
pore.
We
then
these
data
simulations
capable
accurately
reproducing
experimental
performance.
In-depth
gauging
structural
disposition
intercellular
connectivity
allowed
us
improved
computational
predict
relationship
between
study
lays
down
path
advancing
development
silico
tools
biofabricated
evolution
generation,
maps
route
more
biomimetic
manufacture.
next
at
increasing
biological
representativity
minitissues,
implementing
few
changes
(addition
cell-derived
fibroblasts)
hydrogel
(substitution
Matrigel
fibrin)
composition.
also
sought
control
cardiomyocyte
behaviour
based
electrowritten
geometry.
For
this,
hypothesized
diamond-based
would
induce
contraction
direction
least
mechanical
resistance,
i.e.,
small
diagonal
diamonds.
characterization
maturation
consistent
previous
work
terms
gene
although
observed
low
initial
retention
within
highlighted
improve
seeding
efficiency.
comparing
contractile
dynamics
square,
rectangular,
diamond-shaped
pores,
latter
significantly
faster,
stronger
aligned
had
anticipated.
potential
use
agents
tested
implanting
constructs
murine
chronic
myocardial
infarction.
controls,
implanted
animals
showed
improvement,
including
higher
left
ventricular
ejection
fraction
greater
wall
thickness.
Finally,
another
attempt
enhance
constructs,
proof
concept
ellipsoidal
controlled
pore
architecture.
summary,
electrowriting
efforts.
By
both
iteratively
optimising
design
conditions,
increased
relevance.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(20), С. 11000 - 11000
Опубликована: Окт. 12, 2024
Bioassembly
encompasses
various
techniques
such
as
bioprinting,
microfluidics,
organoids,
and
self-assembly,
enabling
advances
in
tissue
engineering
regenerative
medicine.
Advancements
bioassembly
technologies
have
enabled
the
precise
arrangement
integration
of
cell
types
to
more
closely
mimic
complexity
functionality
neurovascular
unit
(NVU)
that
other
biodiverse
multicellular
structures.
In
this
context,
bioprinting
offers
ability
deposit
cells
a
spatially
controlled
manner,
facilitating
construction
interconnected
networks.
Scaffold-based
assembly
strategies
provide
structural
support
guidance
cues
for
growth,
formation
complex
bio-constructs.
Self-assembly
approaches
utilize
inherent
properties
drive
spontaneous
organization
interaction
neuronal
vascular
components.
However,
recreating
intricate
microarchitecture
functional
characteristics
tissue/organ
poses
additional
challenges.
materials
hold
great
promise
addressing
these
The
further
refinement
technologies,
improved
resolution
incorporation
multiple
types,
can
enhance
accuracy
biological
constructs;
however,
developing
bioinks
growth
cells,
viability,
while
maintaining
compatibility
with
process
remains
an
unmet
need
field,
advancements
design
bioactive
biodegradable
scaffolds
will
aid
controlling
adhesion,
differentiation,
vascularization
within
engineered
tissue.
Additionally,
integrating
advanced
imaging
analytical
real-time
monitoring
characterization
bioassembly,
aiding
quality
control
optimization.
While
challenges
remain,
ongoing
research
technological
propel
field
forward,
paving
way
transformative
developments
engineering.
This
work
provides
overview
advancements,
challenges,
future
perspectives
fabricating
constructs
add-on
focus
on
technologies.
Virtual and Physical Prototyping,
Год журнала:
2024,
Номер
19(1)
Опубликована: Ноя. 14, 2024
Diseases
of
the
female
reproductive
tract
can
arise
from
various
congenital
or
acquired
causes
and
may
lead
to
loss
tissue,
functions,
fertility.
Current
treatments
do
not
offer
permanent
solutions,
underscoring
need
for
alternative
therapeutic
approaches.
Tissue
engineering
regenerative
medicine
have
emerged
as
promising
strategies
regenerating
tissues
restoring
3D
bioprinting
technology,
in
particular,
has
exhibited
considerable
potential
treating
tract.
This
review
aims
cover
current
tissue
applications
diseases
highlight
innovative
solutions
offered
by
technology
uterus,
ovary,
cervix,
vagina.
By
assessing
significant
studies
advancements
biomaterials
cell
sources,
this
emphasises
great
enhancing
health
Coatings,
Год журнала:
2023,
Номер
13(8), С. 1345 - 1345
Опубликована: Июль 31, 2023
Hyaluronic
acid
(HA)
is
a
non-sulfated
glycosaminoglycan
(GAG)
that
versatile
material
whose
biological,
chemical,
and
physical
characteristics
can
be
deeply
tuned
to
modifications.
However,
HA
easy
decompose
by
hyaluronidase
in
vivo,
this
process
will
reduce
its
structure
function
stability
during
application.
The
sulfonation
of
improve
under
the
action
hyaluronidase.
Sulfated
hyaluronic
(S-HA)
synthesized
many
methods,
it
shows
significantly
slower
degradation
compared
with
HA.
In
addition,
negatively
charged
S-HA
has
other
advantages
such
as
anti-adhesive
activity,
anti-inflammatory,
macromolecules
electrostatic
interactions,
stable
site
absorption
positively
molecules,
enhancement
growth
factor
binding
ability.
It
numerous
applications
medical
(anti-aging,
inflammation,
tissue
regeneration,
cancer
therapy,
wound
healing,
drug
delivery)
cosmetics
biomaterials
coatings.
article,
advances
for
potential
application
biomedical
coatings
reviewed
comprehensively
discussed.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Июнь 19, 2024
Abstract
Coronary
atherosclerotic
heart
disease
(CAD)
is
among
the
most
prevalent
chronic
diseases
globally.
Circadian
rhythm
disruption
(CRD)
closely
associated
with
progression
of
various
diseases.
However,
precise
role
CRD
in
development
CAD
remains
to
be
elucidated.
The
score
(CRDscore)
was
employed
quantitatively
assess
level
samples.
Our
investigation
revealed
a
significant
association
between
high
CRDscore
and
adverse
prognosis
patients,
along
substantial
correlation
progression.
Remarkably
distinct
distributions
were
also
identified
subtypes.
In
summary,
we
have
pioneered
revelation
relationship
at
single-cell
established
reliable
markers
for
development,
treatment,
CAD.
A
deeper
understanding
these
mechanisms
may
offer
new
possibilities
incorporating
"the
therapy
coronary
based
circadian
rhythm"
into
personalized
medical
treatment
regimens.
Various
systemic
metabolic
diseases
arise
from
prolonged
crosstalk
across
multiple
organs,
triggering
serious
impairments
in
various
physiological
systems.
These
are
intricate
pathologies
characterized
by
complex
mechanisms
and
an
unclear
etiology,
making
the
treatment
challenging.
Efforts
have
been
made
to
develop
vitro
models
understand
these
devise
new
treatments.
However,
there
limitations
reconstructing
causal
relationships
between
interorgan
crosstalk,
including
tissue-specific
microenvironment.
Alternatively,
multi-organ
microphysiological
systems
(MOMPS)
present
possibilities
for
capturing
complexity
of
replicating
human
microphysiology
simulating
diverse
crosstalk.
Controlled
interactions
scalable
representations
biological
MOMPS
offer
a
more
accurate
portrayal
organ
interactions,
enabling
identification
novel
metabolism,
immunity.
This,
turn,
can
yield
valuable
insights
into
disease
drug
development
research
enhance
efficiency
preclinical
studies.
In
this
review,
examples
technical
capabilities
pathological
modeling
discussed,
leveraging
state-of-the-art
biofabrication
technology
MOMPS.
It
evaluates
current
opportunities
challenges
field.
BioMedical Engineering OnLine,
Год журнала:
2024,
Номер
23(1)
Опубликована: Ноя. 6, 2024
Vascular
transplantation
is
an
effective
treatment
for
severe
vascular
lesions.
The
design
of
the
bioactive
and
mechanical
properties
small-caliber
grafts
critical
their
application
in
tissue
engineering.
In
this
study,
we
sought
to
develope
a
graft
by
electrospinning
mixture
human
acellular
amniotic
membrane
(HAAM)
polycaprolactone
(PCL).
Mechanical
tests
showed
that
were
strong
enough
endure
stress
from
adjacent
blood
vessels
pressure.
biocompatibility
HAAM/PCL
was
evaluated
based
on
cell
proliferation
vitro.
tubular
formation
test
demonstrated
containing
HAAM
could
improve
umbilical
vein
endothelial
function,
vivo
implantation
performed
replacing
rat
abdominal
aorta.
found
promote
attachment
retention.
regenerated
smooth
muscle
layer
similar
native
arteries'
endothelium
coverage
complete.
These
results
suggest
our
constructs
may
be
promising
candidates
can
potentially
used
develop
endothelialize
rapidly
vivo.
Materials,
Год журнала:
2024,
Номер
17(22), С. 5607 - 5607
Опубликована: Ноя. 16, 2024
With
the
continuous
progress
of
biomedical
technology,
biomaterial
coatings
play
an
important
role
in
improving
performance
medical
devices
and
promoting
tissue
repair
regeneration.
The
application
natural
medicine
to
biological
materials
has
become
a
hot
topic
due
its
diverse
activity,
low
toxicity,
wide
range
sources.
This
article
introduces
definition
classification
medicines,
lists
some
common
such
as
curcumin,
allicin,
chitosan,
tea
polyphenols,
etc.,
activities
antibacterial,
antioxidant,
antitumor,
other
properties.
According
different
characteristics
physical
adsorption,
chemical
grafting,
layer-by-layer
self-assembly,
sol-gel
methods
are
combined
with
biomaterials,
which
can
be
used
for
orthopedic
implants,
cardiovascular
cerebrovascular
stents,
wound
dressings,
drug
delivery
systems,
exert
their
activity.
For
example,
antibacterial
properties,
regeneration,
biocompatibility
promote
development
health.
Although
biomaterials
been
greatly
expanded,
it
still
faces
major
challenges,
whether
combination
between
coating
substrate
is
firm,
load
released
sustainably,
dynamic
balance
will
disrupted,
so
on;
series
problems
affects
drugs
coatings.
In
view
these
problems,
this
paper
summarizes
suggestions
by
evaluating
literature,
optimizing
binding
method
release
system;
carrying
out
more
clinical
research;
multidisciplinary
cooperation;
broadening
coatings;
developing
safer,
effective
multi-functional
through
research
innovation,
contribute
field.
Chemical Society Reviews,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 28, 2024
We
propose
a
simplified
two-layered
model
of
native
tubular
tissues,
based
on
the
composition
and
structure.
This
approach
offers
guidelines
to
elaborate
biomimetic
materials
in
field
tissue
engineering
for
clinical
applications.
The
adult
human
heart
has
evolved
to
become
a
highly
specialized
organ,
whose
continuous
pumping
of
blood
is
critical
for
survival.
However,
its
ability
regenerate
or
self-repair
following
injury
very
limited,
so
consequently
any
event
disease
resulting
in
damage
the
poses
serious
threat
patient.
Moreover,
cardiovascular
diseases
represent
one
most
pressing
healthcare
concerns
nowadays,
as
they
are
leading
cause
death
worldwide,
and
number
cases
only
expected
increase
years.
Despite
great
progress
made
over
years
treat
diseases,
date
there
no
therapy
able
fully
cure
that
been
damaged.
In
consequence,
dire
need
generate
new
strategies
repair
restore
lost
cardiac
function,
well
develop
accurate
modelling
platforms
advance
understanding
progression
assess
effectiveness
drugs.
Since
advent,
tissue
engineering
regenerative
medicine
regarded
promising
candidate
realise
this
enormous
challenge.
Given
interdisciplinary
nature,
scientific
breakthroughs
different
areas
such
cellular
reprogramming,
polymer
chemistry,
additive
manufacturing
technologies
have
resulted
advancement
One
cornerstone
discoveries
was
generation
induced
pluripotent
stem
cells
subsequent
differentiation
phenotypes,
present
Thesis
revolves
around
their
application
patient-specific
models
humanised
engineered
functional
minitissues.
Firstly,
we
reprogrammed
peripheral
mononuclear
from
transthyretin
amyloid
cardiomyopathy
patient,
cell
line
carrying
c.128G>A
(p.Ser43Asn)
mutation
gene.
Experiments
demonstrated
efficacy
safety
approach,
confirming
pluripotency
cells,
presence
disease-causing
mutation,
removal
reprogramming
vectors.
This
line,
which
now
available
repository,
can
be
used
investigate
biology,
molecular
mechanisms
progression;
an
advanced
model
test
novel
therapeutic
strategies.
Secondly,
aimed
minitissues
by
combining
cardiomyocytes
derived
tridimensional
fibrillar
scaffolds
generated
with
technology
melt
electrowriting.
Compared
conventional
two-dimensional
culture,
enhanced
maturation,
significant
conduction
velocity,
connexin
43
expression
cardiac-associated
genes
MYL2,
GJA5
SCN5A,
isoform
ratios
MYH7/MYH6
MYL2/MYL7
after
28
days
culture.
When
investigating
effect
scaffold
fibres
on
found
placed
close
fibre
were
arranged
parallel
it,
but
alignment
progressively
towards
centre
pore.
We
then
these
data
simulations
capable
accurately
reproducing
experimental
performance.
In-depth
gauging
structural
disposition
intercellular
connectivity
allowed
us
improved
computational
predict
relationship
between
study
lays
down
path
advancing
development
silico
tools
biofabricated
evolution
generation,
maps
route
more
biomimetic
manufacture.
next
at
increasing
biological
representativity
minitissues,
implementing
few
changes
(addition
cell-derived
fibroblasts)
hydrogel
(substitution
Matrigel
fibrin)
composition.
also
sought
control
cardiomyocyte
behaviour
based
electrowritten
geometry.
For
this,
hypothesized
diamond-based
would
induce
contraction
direction
least
mechanical
resistance,
i.e.,
small
diagonal
diamonds.
characterization
maturation
consistent
previous
work
terms
gene
although
observed
low
initial
retention
within
highlighted
improve
seeding
efficiency.
comparing
contractile
dynamics
square,
rectangular,
diamond-shaped
pores,
latter
significantly
faster,
stronger
aligned
had
anticipated.
potential
use
agents
tested
implanting
constructs
murine
chronic
myocardial
infarction.
controls,
implanted
animals
showed
improvement,
including
higher
left
ventricular
ejection
fraction
greater
wall
thickness.
Finally,
another
attempt
enhance
constructs,
proof
concept
ellipsoidal
controlled
pore
architecture.
summary,
electrowriting
efforts.
By
both
iteratively
optimising
design
conditions,
increased
relevance.