Frontiers in Cell and Developmental Biology,
Journal Year:
2022,
Volume and Issue:
9
Published: Jan. 5, 2022
Osteoblasts
continuously
replenished
by
osteoblast
progenitor
cells
form
the
basis
of
bone
development,
maintenance,
and
regeneration.
Mesenchymal
stem
(MSCs)
from
various
tissues
can
differentiate
into
cell
osteogenic
lineage
serve
as
main
source
osteoblasts.
They
also
respond
flexibly
to
regenerative
anabolic
signals
emitted
surrounding
microenvironment,
thereby
maintaining
homeostasis
participating
in
remodeling.
However,
MSCs
exhibit
heterogeneity
at
multiple
levels
including
different
tissue
sources
subpopulations
which
diversified
gene
expression
differentiation
capacity,
surface
markers
used
predict
potential
remain
be
further
elucidated.
The
rapid
advancement
tracing
methods
single-cell
technology
has
made
substantial
progress
characterization
stem/progenitor
populations
MSCs.
Here,
we
reviewed
research
scRNA-seq
identification
pathways,
MSC-related
new
insights
drawn
combined
with
experimental
technology,
recent
findings
regarding
interaction
between
fate
niche
pathological
process.
Molecular Metabolism,
Journal Year:
2022,
Volume and Issue:
58, P. 101450 - 101450
Published: Feb. 2, 2022
As
common
progenitor
cells
of
osteoblasts
and
adipocytes,
bone
marrow
mesenchymal
(stromal)
stem
(BMSCs)
play
key
roles
in
homeostasis,
tissue
regeneration,
global
energy
homeostasis;
however,
the
intrinsic
mechanism
BMSC
differentiation
is
not
well
understood.
Plasticity
metabolism
allows
BMSCs
to
match
divergent
demands
osteo-adipogenic
differentiation.
Targeting
metabolic
pathways
may
provide
a
novel
therapeutic
perspective
for
unbalance
related
diseases.
This
review
covers
recent
studies
glucose,
fatty
acids,
amino
acids
fuel
We
also
discuss
findings
about
Glucose,
Moreover,
some
well-known
regulators
including
environmental
stress,
hormone
drugs,
biological
pathological
factors
influence
by
altering
metabolism.
offers
insight
significance
on
fate
determination
provides
possibility
treating
diseases
differentiation,
such
as
obesity
osteoporosis,
from
perspective.
Bone Research,
Journal Year:
2022,
Volume and Issue:
10(1)
Published: Oct. 19, 2022
Abstract
The
tissue-resident
skeletal
stem
cells
(SSCs),
which
are
self-renewal
and
multipotent,
continuously
provide
(including
chondrocytes,
bone
cells,
marrow
adipocytes,
stromal
cells)
for
the
development
homeostasis
of
system.
In
recent
decade,
utilizing
fluorescence-activated
cell
sorting,
lineage
tracing,
single-cell
sequencing,
studies
have
identified
various
types
SSCs,
plotted
commitment
trajectory,
partially
revealed
their
properties
under
physiological
pathological
conditions.
this
review,
we
retrospect
to
SSCs
identification
functional
studies.
We
discuss
principles
approaches
identify
bona
fide
highlighting
pioneering
findings
that
plot
atlas
SSCs.
roles
progenitors
in
long
bone,
craniofacial
tissues,
periosteum
systematically
discussed.
further
focus
on
disputes
challenges
SSC
research.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Jan. 28, 2022
Abstract
Developmental
osteogenesis,
physiological
bone
remodelling
and
fracture
healing
require
removal
of
matrix
cellular
debris.
Osteoclasts
generated
by
the
fusion
circulating
monocytes
degrade
bone,
whereas
identity
cells
responsible
for
cartilage
resorption
is
a
long-standing
controversial
question.
Here
we
show
that
degradation
chondrocyte
phagocytosis
are
mediated
fatty
acid
binding
protein
5-expressing
representing
septoclasts,
which
have
mesenchymal
origin
not
derived
from
haematopoietic
cells.
The
Notch
ligand
Delta-like
4,
provided
endothelial
cells,
necessary
septoclast
specification
developmental
growth.
Consistent
with
termination
growth,
septoclasts
disappear
in
adult
ageing
but
re-emerge
association
growing
vessels
during
healing.
We
propose
rare,
specialized
distinct
osteoclasts.
Our
findings
implications
healing,
frequently
impaired
aging
humans.
Bone Research,
Journal Year:
2023,
Volume and Issue:
11(1)
Published: Feb. 24, 2023
Although
previous
RNA
sequencing
methods
have
been
widely
used
in
orthopedic
research
and
provided
ideas
for
therapeutic
strategies,
the
specific
mechanisms
of
some
disorders,
including
osteoarthritis,
lumbar
disc
herniation,
rheumatoid
arthritis,
fractures,
tendon
injuries,
spinal
cord
injury,
heterotopic
ossification,
osteosarcoma,
require
further
elucidation.
The
emergence
single-cell
(scRNA-seq)
technique
has
introduced
a
new
era
on
these
topics,
as
this
method
provides
information
regarding
cellular
heterogeneity,
cell
subtypes,
functions
novel
subclusters,
potential
molecular
mechanisms,
cell-fate
transitions,
cell‒cell
interactions
that
are
involved
development
diseases.
Here,
we
summarize
subpopulations,
genes,
underlying
diseases
identified
by
scRNA-seq,
improving
our
understanding
pathology
providing
insights
into
approaches.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(8)
Published: Feb. 23, 2024
Skeletal
stem
cells
(SSCs)
that
are
capable
of
self-renewal
and
multipotent
differentiation
contribute
to
bone
development
homeostasis.
Several
populations
SSCs
at
different
skeletal
sites
have
been
reported.
Here,
we
identify
a
metaphyseal
SSC
(mpSSC)
population
whose
transcriptional
landscape
is
distinct
from
other
mesenchymal
stromal
(BMSCs).
These
mpSSCs
marked
by
Sstr2
or
Pdgfrb
+
Kitl
−
,
located
just
underneath
the
growth
plate,
exclusively
derived
hypertrophic
chondrocytes
(HCs).
HC-derived
properties
multipotency
in
vitro
vivo,
producing
most
HC
offspring
postnatally.
HC-specific
deletion
Hgs,
component
endosomal
sorting
complex
required
for
transport,
impairs
HC-to-mpSSC
conversion
compromises
trabecular
formation.
Thus,
mpSSC
major
source
BMSCs
osteoblasts
marrow,
supporting
postnatal
Journal of Biological Chemistry,
Journal Year:
2024,
Volume and Issue:
300(4), P. 107158 - 107158
Published: March 11, 2024
Single-cell
RNA
sequencing
has
led
to
novel
designations
for
mesenchymal
cells
associated
with
bone
as
well
multiple
what
appear
be
the
same
cell
type.
The
main
goals
of
this
study
were
increase
amount
single
sequence
data
osteoblasts
and
osteocytes,
compare
from
periosteum
those
inside
bone,
clarify
major
categories
types
murine
bone.
We
created
an
atlas
bone-associated
by
harmonizing
published
datasets
in-house
targeted
Osx1-Cre
Dmp1-Cre
driver
strains.
Cells
periosteal
analyzed
separately
isolated
endosteum
trabecular
Over
100,000
mapped
reveal
11
clusters
designated
fibro-1,
fibro-2,
chondrocytes,
articular
tenocytes,
adipo-CAR,
osteo-CAR,
pre-osteoblasts,
osteoblasts,
osteo-X,
latter
defined
in
part
Postn
expression.
Osteo-X,
pre-osteoblasts
closely
at
surface.
Wnt16
was
expressed
but
not
endocortical
or
cancellous
Fibro-2
cells,
which
express
markers
stem
localized
adult
mice.
Suppressing
remodeling
eliminated
altered
gene
expression
did
change
abundance
location
osteo-X
osteo-CAR
cells.
These
results
provide
a
framework
identifying
suggest
that
osteoblast
progenitors
reside
near
surface