Current Opinion in Cell Biology,
Journal Year:
2024,
Volume and Issue:
88, P. 102345 - 102345
Published: March 12, 2024
Cell
migration
plays
a
pivotal
role
in
various
biological
processes
including
cancer
dissemination
and
successful
metastasis,
where
the
of
mechanical
signals
is
increasingly
acknowledged.
This
review
focuses
on
intricate
mechanisms
through
which
cells
modulate
their
migratory
strategies
via
organelle
adaptations
response
to
extracellular
matrix
(ECM).
Specifically,
nucleus
mitochondria
emerge
as
mediators
this
process.
These
organelles
serve
sensors,
translating
stimuli
into
rapid
metabolic
alterations
that
sustain
cell
migration.
Importantly,
prolonged
exposure
such
can
induce
transcriptional
or
epigenetic
changes,
ultimately
enhancing
metastatic
traits.
Deciphering
interplay
between
ECM
properties
not
only
advances
our
understanding
cytoskeletal
dynamics
but
also
holds
promise
for
development
innovative
anti-metastatic
therapeutic
strategies.
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(21)
Published: Jan. 15, 2024
Microfluidic
chips
are
valuable
tools
for
studying
intricate
cellular
and
cell-microenvironment
interactions.
Traditional
in
vitro
cancer
models
lack
accuracy
mimicking
the
complexities
of
vivo
tumor
microenvironment.
However,
cancer-metastasis-on-a-chip
(CMoC)
combine
advantages
3D
cultures
microfluidic
technology,
serving
as
powerful
platforms
exploring
mechanisms
facilitating
drug
screening.
These
able
to
compartmentalize
metastatic
cascade,
deepening
understanding
its
underlying
mechanisms.
This
article
provides
an
overview
current
CMoC
models,
focusing
on
distinctive
that
simulate
invasion,
intravasation,
circulation,
extravasation,
colonization,
their
applications
Furthermore,
challenges
faced
by
technologies
discussed,
while
promising
future
directions
research.
The
ongoing
development
integration
these
into
studies
expected
drive
transformative
advancements
field.
Journal of Biological Engineering,
Journal Year:
2024,
Volume and Issue:
18(1)
Published: April 8, 2024
Inertial
effects
caused
by
perturbations
of
dynamical
equilibrium
during
the
flow
soft
matter
constitute
a
hallmark
turbulence.
Such
are
attributable
to
an
imbalance
between
energy
storage
and
dissipation.
During
Newtonian
fluids,
kinetic
can
be
both
stored
dissipated,
while
viscoelastic
systems,
such
as
polymer
induces
accumulation
elastic
energies.
The
causes
local
stiffening
stretched
chains,
which
destabilise
flow.
Migrating
multicellular
systems
hugely
complex
capable
self-regulating
their
viscoelasticity
mechanical
stress
generation,
well
controlling
Since
perturbation
is
inhomogeneous
energy,
rather
than
turbulence
occur
at
low
Reynolds
numbers.This
theoretical
review
focused
on
clarifying
role
in
appearance
low-Reynolds
Three
types
system
considered
compared:
(1)
high-Reynolds
turbulent
(2)
moderate-Reynolds
solutions,
(3)
migration
epithelial
collectives,
discussed
terms
two
model
systems.
models
involve
fusion
aggregates,
free
expansion
monolayers
substrate
matrix.
Lab on a Chip,
Journal Year:
2024,
Volume and Issue:
24(7), P. 2094 - 2106
Published: Jan. 1, 2024
Organ-on-chip
(OOC)
technology
has
recently
emerged
as
a
powerful
tool
to
mimic
physiological
or
pathophysiological
conditions
through
cell
culture
in
microfluidic
devices.
One
of
its
main
goals
is
bypassing
animal
testing
and
encouraging
more
personalized
medicine.
The
recent
incorporation
hydrogels
3D
scaffolds
into
devices
changed
biomedical
research
since
they
provide
biomimetic
extracellular
matrix
recreate
tissue
architectures.
However,
this
presents
some
drawbacks
such
the
necessity
for
physical
structures
pillars
confine
these
hydrogels,
well
difficulty
reaching
different
shapes
patterns
create
convoluted
gradients
realistic
biological
structures.
In
addition,
can
also
interfere
with
fluid
flow,
altering
local
shear
forces
and,
therefore,
modifying
mechanical
environment
OOC
model.
work,
we
present
methodology
based
on
plasma
surface
treatment
that
allows
building
chambers
abutment-free
capable
producing
precise
stress
distributions.
Therefore,
pillarless
arbitrary
geometries
are
needed
obtain
versatile,
reliable,
experimental
models.
Through
computational
simulation
studies,
changes
demonstrated
designed
fabricated
geometries.
To
prove
versatility
new
technique,
blood-brain
barrier
model
been
recreated,
achieving
an
uninterrupted
endothelial
emulates
part
neurovascular
network
brain.
Finally,
developed
could
avoid
limitations
mentioned
above,
allowing
development
models
complex
adaptable
geometries,
cell-to-cell
contact
if
required,
where
flow
be
controlled.
Nanomaterials,
Journal Year:
2024,
Volume and Issue:
14(9), P. 760 - 760
Published: April 26, 2024
Currently,
a
major
challenge
in
material
engineering
is
to
develop
cell-safe
biomaterial
with
significant
utility
processing
technology
such
as
3D
bioprinting.
The
main
goal
of
this
work
was
optimize
the
composition
new
graphene
oxide
(GO)-based
bioink
containing
additional
extracellular
matrix
(ECM)
unique
properties
that
may
find
application
bioprinting
biomimetic
scaffolds.
experimental
evaluated
functional
viscosity
and
complex
modulus,
printability,
mechanical
strength,
elasticity,
degradation
absorbability,
well
biological
cytotoxicity
cell
response
after
exposure
biomaterial.
findings
demonstrated
inclusion
GO
had
no
substantial
impact
on
rheological
but
it
did
enhance
properties.
This
enhancement
crucial
for
advancement
scaffolds
are
resilient
deformation
promote
their
utilization
tissue
investigations.
Furthermore,
GO-based
hydrogels
exhibited
much
greater
swelling,
absorbability
compared
non-GO-based
bioink.
Additionally,
these
biomaterials
showed
lower
cytotoxicity.
Due
its
properties,
recommended
use
models
vascular
system,
e.g.,
testing
drugs
or
hard
models.
The
development
of
stable
and
standardized
in
vitro
cytotoxicity
testing
models
is
essential
for
drug
discovery
personalized
medicine.
Microfluidic
technologies,
recognized
their
small
size,
reduced
reagent
consumption,
control
over
experimental
variables,
have
gained
considerable
attention.
However,
challenges
associated
with
external
pumps,
particularly
inconsistencies
between
individual
pumping
systems,
limited
the
real-world
application
cancer-on-a-chip
technology.
This
study
introduces
a
novel
triplicate
cell
culture
system
(Tri-CS)
that
simultaneously
supports
dynamic
cultures
three
independent
units
using
single
peristaltic
pump,
ensuring
consistent
flow
conditions.
Our
findings
demonstrate
Tri-CS
significantly
reduces
variability
compared
to
pump
enhancing
reliability
anticancer
testing.
Furthermore,
we
evaluated
gemcitabine
cytotoxicity,
which
shows
enhanced
efficacy
Fluorescein
diffusion
tests
revealed
greater
efficiency
cultures,
contributed
higher
observed
efficacy.
potential
broader
Tri-CS,
including
its
compatibility
commercially
available
transwells
opportunity
use
more
complex
cancer-on-chip
models,
positions
this
as
valuable
tool
advancing
microphysiological
systems
preclinical
research.
Journal of The Royal Society Interface,
Journal Year:
2025,
Volume and Issue:
22(222)
Published: Jan. 1, 2025
Culturing
living
cells
in
three-dimensional
environments
increases
the
biological
relevance
of
laboratory
experiments,
but
requires
solutes
to
overcome
a
diffusion
barrier
reach
centre
cellular
constructs.
We
present
theoretical
and
numerical
investigation
that
brings
mechanistic
understanding
how
microfluidic
culture
conditions,
including
chamber
size,
inlet
fluid
velocity
spatial
confinement,
affect
solute
distribution
within
Contact
with
substrate
reduces
maximally
achievable
construct
radius
by
15%.
In
practice,
finite
convection
kinetics
further
lower
limit.
The
benefits
external
are
greater
if
transport
rates
across
diffusion-dominated
areas
high.
Those
omnipresent
include
diffusive
boundary
layer
growing
from
fluid–construct
interface
regions
near
corners
where
is
recirculating.
Such
multiply
required
achieve
given
penetration
up
100,
so
chip
designs
ought
minimize
them.
Our
results
define
conditions
complete
into
an
avascular
cell
applies
real
chambers
without
needing
simulate
their
exact
geometries.
The Journal of Physiology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 20, 2025
Abstract
Haemodialysis
(HD)
is
often
required
for
patients
with
end‐stage
renal
disease.
Arteriovenous
fistulas
(AVFs),
a
surgical
procedure
connecting
an
artery
to
vein,
are
the
preferred
vascular
access
HD
due
their
durability
and
lower
complication
rates.
The
aim
of
AVFs
promote
vein
remodelling
accommodate
increased
blood
flow
needed
dialysis.
However,
many
fail
mature
properly,
making
them
unsuitable
Successful
maturation
requires
remodelling,
resulting
in
luminal
diameter
thickened
walls
support
flow.
After
AVF
creation,
haemodynamic
changes
on
venous
side
initiate
cascade
events
that,
when
successful,
lead
proper
AVF,
it
suitable
cannulation.
In
this
process,
endothelial
cells
play
crucial
role
since
they
direct
contact
frictional
forces
exerted
by
blood,
known
as
shear
stress.
Patients
requiring
have
other
conditions
that
increase
burden
senescent
cells,
such
ageing,
diabetes
hypertension.
These
characterized
irreversible
growth
arrest
secretion
pro‐inflammatory
pro‐thrombotic
factors,
collectively
senescence‐associated
secretory
phenotype
(SASP).
This
accumulation
can
impair
function
promoting
inflammation,
reducing
vasodilatation,
increasing
thrombosis
risk,
thus
hindering
function.
review
explores
contribution
potential
therapeutic
strategies
alleviate
effects
cell
accumulation,
aiming
improve
image
ACS Applied Materials & Interfaces,
Journal Year:
2025,
Volume and Issue:
17(9), P. 13358 - 13374
Published: Feb. 20, 2025
The
fairness
of
long-term
self-renewal
and
robust
cell
proliferation
limits
the
applications
human
mesenchymal
stem
cells
(hMSCs)
in
regenerative
medicine.
Inducing
hMSCs
from
human-induced
pluripotent
(hiPSCs),
which
have
advantages
autogenous
no
number
issues,
is
highly
valuable.
However,
current
induction
methods
using
FBS-containing
culture
medium
problems,
including
immunogenicity,
microbial
contamination,
low
efficiency.
To
solve
these
we
propose
a
chemically
defined
protocol
incorporating
transforming
growth
factor-beta
1
retinoic
acid
(RA)
additives
serum-free
E6
for
suspension
embryoid
bodies
hiPSCs.
Additionally,
microgroove-patterned
polydimethylsiloxane
surfaces
coated
with
temperature-sensitive
N-isopropylacrylamide
(PNIPAAm)
were
prepared
efficient
harvesting
purification
induced
hiPSC-derived
(hiPSC-MSCs).
results
showed
that
both
supplementation
RA
patterned
microgrooves
width
20
μm
could
accelerate
hiPSC-MSCs,
realizing
promising
scalable
production
homogeneous
cells.
This
study
successfully
established
utilized
to
obtain
clinically
applicable
show
great
promise
tissue
engineering,
gene
therapy,
transplantation.
Biofilm,
Journal Year:
2025,
Volume and Issue:
9, P. 100267 - 100267
Published: Feb. 28, 2025
Colonization
of
medical
devices
by
microorganisms,
often
progressing
to
the
formation
resilient
biofilms,
presents
a
common
clinical
issue.
To
address
this
challenge,
there
is
growing
interest
in
developing
novel
biomaterials
with
antimicrobial/antibiofilm
properties
as
promising
preventive
measure.
This
study
explores
nanocomposite
based
on
silver
nanoparticles
(AgNPs)
deposited
thin
silica
(SiO2)
layers
for
their
potential
effect
adhesion,
detachment,
viability
and
biofilm
opportunistic
Pseudomonas
aeruginosa.
The
AgNPs-based
biointerface
development
investigated
PAO1-Tn7-gfp
strain
combining
experiments
under
static
dynamic
conditions.
For
latter,
shear-stress
flow
chamber
used
mimic
conditions
encountered
around
certain
devices.
findings
reveal
rapid
bactericidal
AgNPs,
noticeable
within
30
min
exposure.
Moreover,
delay
surface
colonization
observed
unstructured
biofilm,
even
after
72h
culture.
A
considerable
fragility
sensitivity
hydrodynamic
stresses
noticed
loosely
attached
bacterial
monolayer
when
compared
thick
formed
SiO2
surface.
underlines
conception
surfaces
controlled
release
biocidal
agent.