Cartilage,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 21, 2025
Objective
This
study
aimed
to
identify
genes
and
signaling
pathways
associated
with
acute
cartilage
injury
using
RNA
sequencing
(RNA-seq).
Methods
Knee
joint
samples
were
collected
from
normal
mice
2
models
of
(non-invasive
groove
models)
within
an
8-hour
time
limit.
RNA-seq
revealed
differential
gene
expression
between
the
controls,
subsequent
validation
real-time
quantitative
polymerase
chain
reaction
(RT-qPCR)
for
9
representative
genes.
Results
Compared
non-invasive
model
showed
36
differentially
expressed
(DEGs)
(13
up-regulated,
23
down-regulated),
Gm14648
Gm35438
showing
most
significant
upregulation
downregulation,
respectively.
The
exhibited
255
DEGs
(222
33
down-regulated).
Six
overlapping
identified
models,
including
up-regulated
(
Igfn1,
Muc6,
Hmox1
)
down-regulated
Pthlh,
Cyp1a1,
Gm13490
),
validated
by
RT-qPCR.
Gene
ontology
(GO)
analysis
highlighted
involvement
in
environmental
information
processing
organ
system
function,
while
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
implicated
JAK-STAT
pathway.
RT-qPCR
immunohistochemistry
confirmed
downregulation
Fhl1
model,
supported
Western
blotting
p-JAK2/t-JAK2
levels.
Conclusions
identifies
injury,
suggesting
potential
therapeutic
targets.
role
protection
via
pathway
warrants
further
investigation
research.
Computational and Structural Biotechnology Journal,
Journal Year:
2025,
Volume and Issue:
27, P. 265 - 277
Published: Jan. 1, 2025
Despite
the
wealth
of
single-cell
multi-omics
data,
it
remains
challenging
to
predict
consequences
novel
genetic
and
chemical
perturbations
in
human
body.
It
requires
knowledge
molecular
interactions
at
all
biological
levels,
encompassing
disease
models
humans.
Current
machine
learning
methods
primarily
establish
statistical
correlations
between
genotypes
phenotypes
but
struggle
identify
physiologically
significant
causal
factors,
limiting
their
predictive
power.
Key
challenges
modeling
include
scarcity
labeled
generalization
across
different
domains,
disentangling
causation
from
correlation.
In
light
recent
advances
data
integration,
we
propose
a
new
artificial
intelligence
(AI)-powered
biology-inspired
multi-scale
framework
tackle
these
issues.
This
will
integrate
organism
hierarchies,
species
genotype-environment-phenotype
relationships
under
various
conditions.
AI
inspired
by
biology
may
targets,
biomarkers,
pharmaceutical
agents,
personalized
medicines
for
presently
unmet
medical
needs.
IEEE Transactions on Fuzzy Systems,
Journal Year:
2024,
Volume and Issue:
32(8), P. 4448 - 4459
Published: May 13, 2024
Single-cell
multi-view
clustering
is
essential
for
analyzing
the
different
cell
subtypes
of
same
from
views.
Some
attempts
have
been
made,
but
most
these
models
still
struggle
to
handle
single-cell
sequencing
data,
primarily
due
their
non-specific
design
cellular
data.
We
observe
that
such
data
distinctively
exhibits:
(1)
a
profusion
high-order
topological
correlations,
(2)
disparate
distribution
information
across
views,
and
(3)
inherent
fuzzy
characteristics,
indicating
cell's
potential
associate
with
multiple
cluster
identities.
Neglecting
key
patterns
could
significantly
impair
medical
clustering.
In
response,
we
propose
specialized
application
namely
deep
Multi-view
Fuzzy
Clustering
(scMFC)
method.
Concretely,
employ
random
walk
technique
capture
relationships
on
graph
developed
cross-view
aggregation
mechanism
adaptively
assigns
weights
Furthermore,
accurately
reflect
dynamic
insight
in
development,
strategy
allows
cells
diverse
clusters.
Extensive
experiments
conducted
three
real-world
datasets
demonstrate
our
method's
superior
performance.
Biology,
Journal Year:
2024,
Volume and Issue:
13(11), P. 848 - 848
Published: Oct. 22, 2024
With
the
advent
of
high-throughput
technologies,
field
omics
has
made
significant
strides
in
characterizing
biological
systems
at
various
levels
complexity.
Transcriptomics,
proteomics,
and
metabolomics
are
three
most
widely
used
each
providing
unique
insights
into
different
layers
a
system.
However,
analyzing
data
set
separately
may
not
provide
comprehensive
understanding
subject
under
study.
Therefore,
integrating
multi-omics
become
increasingly
important
bioinformatics
research.
In
this
article,
we
review
strategies
for
transcriptomics,
data,
including
co-expression
analysis,
metabolite-gene
networks,
constraint-based
models,
pathway
enrichment
interactome
analysis.
We
discuss
combined
integration
approaches,
correlation-based
strategies,
machine
learning
techniques
that
utilize
one
or
more
types
data.
By
presenting
these
methods,
aim
to
researchers
with
better
how
integrate
gain
view
system,
facilitating
identification
complex
patterns
interactions
might
be
missed
by
single-omics
analyses.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(11), P. 5951 - 5951
Published: May 29, 2024
Maternal
obesity
and
over/undernutrition
can
have
a
long-lasting
impact
on
offspring
health
during
critical
periods
in
the
first
1000
days
of
life.
Children
born
to
mothers
with
reduced
immune
responses
stimuli
which
increase
susceptibility
infections.
Recently,
maternal
western-style
diets
(WSDs),
high
fat
simple
sugars,
been
associated
skewing
neonatal
cell
development,
recent
evidence
suggests
that
dysregulation
innate
immunity
early
life
has
long-term
consequences
metabolic
diseases
behavioral
disorders
later
Several
factors
contribute
abnormal
tolerance
or
trained
immunity,
including
changes
gut
microbiota,
metabolites,
epigenetic
modifications.
Critical
knowledge
gaps
remain
regarding
mechanisms
whereby
these
fetal
postnatal
especially
precursor
stem
cells
bone
marrow
liver.
Components
microbiota
are
transferred
from
consuming
WSD
their
understudied
identifying
cause
effect
adaptive
development
needs
be
refined.
Tools
single-cell
RNA-sequencing,
analysis,
spatial
location
specific
liver
for
understanding
system
programming.
Considering
vital
role
function
plays
health,
it
will
important
understand
how
control
developmental
programming
immunity.
Frontiers in Endocrinology,
Journal Year:
2024,
Volume and Issue:
15
Published: July 11, 2024
Spermatogenesis
is
a
multi-step
biological
process
where
mitotically
active
diploid
(2n)
spermatogonia
differentiate
into
haploid
(n)
spermatozoa
via
regulated
meiotic
programming.
The
alarming
rise
in
male
infertility
has
become
global
concern
during
the
past
decade
thereby
demanding
an
extensive
profiling
of
testicular
gene
expression.
Advancements
Next-Generation
Sequencing
(NGS)
technologies
have
revolutionized
our
empathy
towards
complex
events
including
spermatogenesis.
However,
despite
multiple
attempts
made
to
reveal
transcriptional
signature(s)
either
with
bulk
tissues
or
at
single-cell,
level,
comprehensive
reviews
on
transcriptomics
and
associated
disorders
are
limited.
Notably,
explicating
genome-wide
expression
patterns
various
stages
spermatogenic
progression
provide
dynamic
molecular
landscape
transcription.
Our
review
discusses
advantages
single-cell
RNA-sequencing
(Sc-RNA-seq)
over
RNA-seq
concerning
tissues.
Additionally,
we
highlight
cellular
heterogeneity,
spatial
transcriptomics,
cell-to-cell
interactions
distinct
cell
populations
within
testes
germ
cells
(Gc),
Sertoli
(Sc),
Peritubular
(PTc),
Leydig
(Lc),
etc.
Furthermore,
summary
key
finding
transcriptomic
studies
that
shed
light
developmental
mechanisms
implicated
infertility.
These
insights
emphasize
pivotal
roles
Sc-RNA-seq
advancing
knowledge
regarding
may
serve
as
potential
resource
formulate
future
clinical
interventions
for
reproductive
health.
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: May 27, 2024
Abstract
A
cell
is
a
dynamic
system
in
which
various
processes
occur
simultaneously.
In
particular,
intra-
and
intercellular
signaling
pathway
crosstalk
has
significant
impact
on
cell’s
life
cycle,
differentiation,
proliferation,
growth,
regeneration,
and,
consequently,
the
normal
functioning
of
an
entire
organ.
Hippo
YAP/TAZ
nucleocytoplasmic
shuttling
play
pivotal
role
development,
homeostasis,
tissue
particularly
lung
cells.
Intersignaling
communication
core
components
localization.
This
review
describes
between
key
pathways
(WNT,
SHH,
TGFβ,
Notch,
Rho,
mTOR)
using
cells
as
example
highlights
remaining
unanswered
questions.
Cell Genomics,
Journal Year:
2024,
Volume and Issue:
4(6), P. 100581 - 100581
Published: May 31, 2024
Cell
atlases
serve
as
vital
references
for
automating
cell
labeling
in
new
samples,
yet
existing
classification
algorithms
struggle
with
accuracy.
Here
we
introduce
SIMS
(scalable,
interpretable
machine
learning
single
cell),
a
low-code
data-efficient
pipeline
single-cell
RNA
classification.
We
benchmark
against
datasets
from
different
tissues
and
species.
demonstrate
SIMS's
efficacy
classifying
cells
the
brain,
achieving
high
accuracy
even
small
training
sets
(<3,500
cells)
across
samples.
accurately
predicts
neuronal
subtypes
developing
shedding
light
on
genetic
changes
during
differentiation
postmitotic
fate
refinement.
Finally,
apply
to
of
cortical
organoids
predict
identities
uncover
variations
between
lines.
identifies
cell-line
differences
misannotated
lineages
human
derived
pluripotent
stem
Altogether,
show
that
is
versatile
robust
tool
cell-type
datasets.
PeerJ,
Journal Year:
2024,
Volume and Issue:
12, P. e17184 - e17184
Published: March 28, 2024
Single-cell
annotation
plays
a
crucial
role
in
the
analysis
of
single-cell
genomics
data.
Despite
existence
numerous
algorithms,
comprehensive
tool
for
integrating
and
comparing
these
algorithms
is
also
lacking.