Kazan medical journal,
Journal Year:
2024,
Volume and Issue:
105(4), P. 648 - 660
Published: July 25, 2024
The
structural
integrity
of
the
skeleton
is
ensured
by
constant
remodeling
bone
tissue,
which
based
on
functioning
and
interaction
osteolytic
cells
(osteoclasts)
tissue
forming
(osteoblasts/osteocytes).
Despite
general
understanding
that
degree
mineralization
matrix
determines
fragility
skeleton,
there
currently
insufficient
information
about
its
age-related
changes
associated
with
these
cells.
purpose
review
to
evaluate
existing
data
functional
state
mesenchymal
stem
cells,
osteoblasts/osteocytes
osteoclasts.
Inclusion
criteria:
randomized
or
non-randomized
controlled
studies
examining
change.
A
search
for
in
field
condition
was
carried
out
electronic
scientific
databases
Google
Scholar,
Medline,
PubMed,
Scopus,
Web
Science
Cochrane
Library
keywords
their
combinations
using
AMSTAR
2
program.
selection
publications
(59
680
included)
randomly,
after
three
authors
independently
assessed
methodological
quality.
main
pathogenetic
mechanism
involved
loss
age
a
decrease
formation
osteoblasts
impairment
ability
osteogenic
differentiation.
Osteocytes
old
are
subject
excessive
prolonged
stress,
causes
unbalanced
autophagy
apoptosis,
leads
deposit
mineralize
extracellular
organic
matrix.
With
age,
accelerated
osteoclastogenesis
occurs,
mediated
osteoblasts,
increased
expression
certain
receptors
at
level
stromal
osteoblasts.
presented
literature
demonstrate
convincing
evidence
an
increase
resorption
due
complex
metabolic
processes
occurs
against
background
number
activity
osteoclasts,
apoptosis
activity,
as
well
redistribution
differentiation
towards
adipocytes.
results
can
be
used
basis
developing
diagnostic
criteria
identifying
senile
osteoporosis
risk
fractures.
Materials Today Bio,
Journal Year:
2023,
Volume and Issue:
22, P. 100741 - 100741
Published: July 20, 2023
Treatment
of
large
bone
defects
represents
a
great
challenge
in
orthopedic
and
craniomaxillofacial
surgery.
Traditional
strategies
tissue
engineering
have
focused
primarily
on
mimicking
the
extracellular
matrix
(ECM)
terms
structure
composition.
However,
synergistic
effects
other
cues
from
microenvironment
during
regeneration
are
often
neglected.
The
is
sophisticated
system
that
includes
physiological
(e.g.,
neighboring
cells
such
as
macrophages),
chemical
oxygen,
pH),
physical
factors
mechanics,
acoustics)
dynamically
interact
with
each
other.
Microenvironment-targeted
increasingly
recognized
crucial
for
successful
offer
promising
solutions
advancing
engineering.
This
review
provides
comprehensive
overview
current
microenvironment-targeted
challenges
further
outlines
prospective
directions
approaches
construction
organoids.
Small,
Journal Year:
2024,
Volume and Issue:
20(33)
Published: March 12, 2024
Abstract
Nanoparticles
of
a
particular,
evolutionarily
old
inorganic
polymer
found
across
the
biological
kingdoms
have
attracted
increasing
interest
in
recent
years
not
only
because
their
crucial
role
metabolism
but
also
potential
medical
applicability:
it
is
polyphosphate
(polyP).
This
ubiquitous
linear
composed
10–1000
phosphate
residues
linked
by
high‐energy
anhydride
bonds.
PolyP
causes
induction
gene
activity,
provides
for
bone
mineralization,
and
serves
as
an
energy
supplier
through
enzymatic
cleavage
its
acid
bonds
subsequent
ATP
formation.
The
biomedical
breakthrough
polyP
came
with
development
successful
fabrication
process,
depot
form,
Ca‐
or
Mg‐polyP
nanoparticles,
directly
effective
polymer,
soluble
Na‐polyP,
regenerative
repair
healing
processes,
especially
tissue
areas
insufficient
blood
supply.
Physiologically,
platelets
are
main
vehicles
nanoparticles
circulating
blood.
To
be
biomedically
active,
these
particles
undergo
coacervation.
review
overview
properties
applications
regeneration
bone,
cartilage,
skin.
In
addition
to
studies
on
animal
models,
first
proof‐of‐concept
humans
chronic
wounds
outlined.
Metabolites,
Journal Year:
2023,
Volume and Issue:
13(4), P. 578 - 578
Published: April 21, 2023
Bone
is
a
dynamic
tissue
composed
of
cells,
an
extracellular
matrix,
and
mineralized
portion.
Osteoblasts
are
responsible
for
proper
bone
formation
remodeling,
function.
These
processes
endergonic
require
cellular
energy
in
the
form
adenosine
triphosphate
(ATP),
which
derived
from
various
sources
such
as
glucose,
fatty
acids,
amino
acids.
However,
other
lipids
cholesterol
have
also
been
found
to
play
critical
role
homeostasis
can
contribute
overall
bioenergetic
capacity
osteoblasts.
In
addition,
several
epidemiological
studies
link
between
elevated
cholesterol,
cardiovascular
disease,
enhanced
risk
osteoporosis,
increased
metastasis
cancer
patients.
This
review
focuses
on
how
its
derivatives,
cholesterol-lowering
medications
(statins)
regulate
osteoblast
function
formation.
It
highlights
molecular
mechanisms
underlying
cholesterol–osteoblast
crosstalk.
Acta Biomaterialia,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 1, 2025
Magnesium
(Mg)-based
implants
have
become
an
attractive
alternative
to
conventional
permanent
in
the
orthopedic
field.
While
biocompatibility,
degradation
kinetics,
and
osseointegration
of
Mg-based
been
mostly
investigated,
impact
products
on
bone
remodeling
potential
systemic
effects
remains
unclear.
The
aim
this
study
was
evaluate
early
mid-term
local
tissue
responses
degrading
ultrahigh-purity
ZX00
(Mg-Zn-Ca
alloy)
Mg
(XHP-Mg)
pins
a
juvenile
healthy
rat
model.
differences
between
implant
types
(degradable
vs.
permanent),
implantation,
age-related
changes
were
investigated
using
titanium
(Ti),
sham-operated,
control
groups
(non-intervention),
respectively.
Degradation
XHP-Mg
promote
osteogenesis
medullary
cavity
by
upregulating
expression
levels
Bmp2
Opg
within
14
days
post-surgery.
higher
rate
resulted
accumulation
starting
from
day
3
upregulation
different
genes,
particularly
Ccl2
Cepbp.
Besides
good
new
formation,
we
found
more
parallel
hydroxyapatite/collagen
orientation
along
perimeter
region
compared
Ti
pins.
In
liver,
reduced
glycogen
indicated
that
glycogenolysis,
while
only
group
showed
serum
glucagon
level
14.
Results
suggest
stimulate
mainly
via
glycogenolysis
genes
metabolites.
STATEMENT
OF
SIGNIFICANCE:
Bioresorbable
magnesium
are
promising
candidates
for
interventions.
Until
now,
few
vivo
studies
explored
how
modulate
responses.
Herein,
results
demonstrate
i)
has
crucial
effect
regulating
cavity,
ii)
HAp/collagen
matrix
pattern
group,
iii)
both
liver.
Our
findings
highlight
dual
role
metabolic
modulation.
Nevertheless,
is
first
report
interaction
liver
metabolism.
Biomaterials Science,
Journal Year:
2023,
Volume and Issue:
11(7), P. 2277 - 2291
Published: Jan. 1, 2023
This
review
highlights
the
importance
of
cell
metabolism
as
a
missing
link
connecting
cellular
behavior
and
physicochemical
properties
biomaterials
serves
guiding
principle
for
designing
scaffolds
bone
tissue
engineering.
Bone Reports,
Journal Year:
2023,
Volume and Issue:
19, P. 101705 - 101705
Published: July 24, 2023
Parathyroid
hormone
acts
through
its
receptor,
PTHR1,
expressed
on
osteoblasts,
to
control
bone
remodeling.
Metabolic
flexibility
for
energy
generation
has
been
demonstrated
in
several
cell
types
dependent
substrate
availability.
Recent
studies
have
identified
a
critical
role
PTH
regulating
glucose,
fatty
acid
and
amino
metabolism
thus
stimulating
both
glycolysis
oxidative
phosphorylation.
Therefore,
we
postulated
that
stimulates
increased
energetic
output
by
osteoblasts
either
increasing
or
phosphorylation
depending
To
test
this
hypothesis,
undifferentiated
differentiated
MC3T3E1C4
calvarial
pre-osteoblasts
were
treated
with
study
osteoblast
bioenergetics
the
presence
of
exogenous
glucose.
Significant
increases
acute
∼1
h
treatment
minimal
effects
glucose
observed.
In
cells,
observed
was
completely
blocked
pretreatment
Glut1
inhibitor
(BAY-876)
resulting
compensatory
increase
We
then
tested
effect
function
complexes
I
II
mitochondrial
electron
transport
chain
absence
glycolysis.
Utilizing
novel
plasma
membrane
permeability
(PMP)
assay,
combination
complex
specific
substrates,
slight
but
significant
basal
maximal
oxygen
consumption
rates
24
cells
noted.
Taken
together,
our
data
demonstrate
first
time
chain,
particularly
II,
during
high
demands
osteoblasts.
Journal of Bone and Mineral Research,
Journal Year:
2024,
Volume and Issue:
39(9), P. 1205 - 1214
Published: June 22, 2024
Abstract
Mitochondria
in
osteoblasts
have
been
demonstrated
to
play
multiple
crucial
functions
bone
formation
from
intracellular
adenosine
triphosphate
production
extracellular
secretion
of
mitochondrial
components.
The
present
review
explores
the
current
knowledge
about
biology
osteoblasts,
including
biogenesis,
bioenergetics,
oxidative
stress
generation,
and
dynamic
changes
morphology.
Special
attention
is
given
recent
findings,
donut
which
actively
generates
mitochondrial-derived
vesicles
(MDVs),
followed
by
small
mitochondria
MDVs.
We
also
discuss
therapeutic
effects
targeting
osteoblast
mitochondria,
highlighting
their
potential
applications
improving
health.