E7 peptide for in situ tissue engineering applications in bone repair
Journal of the American Ceramic Society,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 1, 2025
Abstract
In
regenerative
medicine,
leveraging
bioactive
molecules
to
enhance
endogenous
repair
mechanisms
represents
a
critical
advancement.
The
E7
peptide,
novel
short
has
emerged
as
key
candidate
for
bone
defect
due
its
unique
ability
interact
with
stem
cells
directly.
Unlike
traditional
tissue‐engineered
constructs
that
rely
on
exogenous
cell
delivery
or
scaffold‐based
strategies,
enables
in
situ
regeneration
by
actively
recruiting
and
anchoring
the
site.
Studies
demonstrate
E7‐functionalized
materials
significantly
proliferation
osteogenic
differentiation
while
concurrently
stimulating
local
angiogenesis
through
VEGF
upregulation.
These
dual
effects—stem
homing
vascularization—address
two
major
bottlenecks
repair:
insufficient
supply
poor
nutrient
diffusion
avascular
regions.
Despite
these
advantages,
optimizing
E7's
spatiotemporal
presentation
elucidating
signaling
remain
critical.
Further
investigations
into
receptor
specificity,
dose
dependency,
long‐term
safety
will
accelerate
clinical
translation.
It
is
of
great
guiding
significance
clarify
what
role.
peptide
plays
various
which
pathways
are
activated
future
research
repair.
Language: Английский
Curcumin-Encapsulated Exosomes in Bisphosphonate-Modified Hydrogel Microspheres Promote Bone Repair through Macrophage Polarization and DNA Damage Mitigation
Yunhui Si,
No information about this author
Shuao Dong,
No information about this author
Mengsha Li
No information about this author
et al.
Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
unknown, P. 101874 - 101874
Published: May 1, 2025
Language: Английский
Tailored Pore Architectures in Ti6Al4V Bone Scaffolds for Tunable Permeability and Mechanical Performance
Advanced Engineering Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 19, 2025
To
achieve
multifunctionalities
such
as
nutrient
transport,
cellular
activities,
and
load‐bearing
while
avoiding
stress
shielding,
bone
tissue
engineering
scaffolds
must
exhibit
consistent
permeability
mechanical
properties
comparable
to
those
of
human
bones.
Here,
filament‐rotated,
filament‐shifted,
gradient,
conventional
Ti6Al4V
are
designed
fabricated
using
direct
ink
writing.
These
high‐precision
interconnective
pores
simultaneously
match
the
elastic
modulus
with
trabeculae.
The
impact
internal
pore
architecture
on
is
investigated
systematically
through
experimental
numerical
methods.
Compared
scaffolds,
alterations
in
structure
result
decreased
modulus.
influence
porosity
scaffold
outweighs
that
architecture.
shifted
100%
exhibits
a
more
uniform
symmetrical
distribution
wall
shear
stress,
which
may
promote
cell
adhesion
proliferation.
By
tuning
diverse
architectures,
wide
range
(e.g.,
values
1.12
×
10
−10
2.95
m
2
)
property
moduli
1.0–5.7
GPa)
can
be
achieved.
A
hierarchical,
goal‐oriented
selection
framework
proposed
guide
structural
design
patient‐specific
across
various
anatomical
sites.
Language: Английский