Journal of Nanobiotechnology,
Journal Year:
2023,
Volume and Issue:
21(1)
Published: Dec. 19, 2023
Abstract
Comprehensively
understanding
the
female
reproductive
system
is
crucial
for
safeguarding
fertility
and
preventing
diseases
concerning
women's
health.
With
capacity
to
simulate
intricate
physio-
patho-conditions,
provide
diagnostic
platforms,
microfluidic
chips
have
fundamentally
transformed
knowledge
management
of
health,
which
will
ultimately
promote
development
more
effective
assisted
technologies,
treatments,
drug
screening
approaches.
This
review
elucidates
diverse
systems
in
mimicking
ovary,
fallopian
tube,
uterus,
placenta
cervix,
we
delve
into
culture
follicles
oocytes,
gametes’
manipulation,
cryopreservation,
permeability
especially.
We
investigate
role
microfluidics
endometriosis
hysteromyoma,
explore
their
applications
ovarian
cancer,
endometrial
cancer
cervical
cancer.
At
last,
current
status
technology
integrated
devices
are
introduced
briefly.
Through
delineating
multifarious
advantages
challenges
technology,
chart
a
definitive
course
future
research
woman
health
field.
As
continues
evolve
advance,
it
holds
great
promise
revolutionizing
diagnosis
treatment
issues,
thus
propelling
us
where
can
optimize
overall
wellbeing
women
everywhere.
Graphical
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 6, 2025
Intrauterine
adhesion
(IUA)
has
a
significant
negative
impact
on
women's
reproductive
health.
One
of
the
development
trends
biomaterials
for
prevention
IUA
is
improving
stability
and
multifaceted
functions.
Here,
we
propose
multiresponsive
microcapsule
(A/G-Fe3O4-Se)
with
an
alginate
(ALG)
gelatin
methacryloyl
(GelMA)
dual-network
hydrogel
shell
loaded
magnetic
nanoparticles
(Fe3O4-Se)
ultrasound-responsive
decafluoropentane
core
using
microfluidic
technique.
The
microcapsules
inherited
biofriendly
advantages
ALG
GelMA.
encapsulated
magneto-responsive
Fe3O4-Se
made
flexibly
change
distribution
to
adapt
irregular
shape
uterus
better
exert
therapeutic
effect.
Besides,
A/G-Fe3O4-Se
demonstrated
antioxidant,
antibacterial,
pro-healing
properties
in
vitro.
Moreover,
rat
models,
also
observed
reduction
oxidative
stress,
endometrial
regeneration,
improved
receptivity
pregnancy
rates
after
treatment
microcapsules.
Consequently,
can
be
used
as
promising
strategy
damaged
endometrium
well
IUA.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Feb. 24, 2025
Abstract
Endometriosis
is
a
refractory
estrogen-dependent
gynecological
disease
in
which
ovarian
endometriosis(OE)
the
most
common,
and
main
cell
components
are
endometrial
epithelial
cells
stromal
cells.
However,
constructing
ectopic
models
basic
studies
still
challenging.
In
this
study,
we
explored
feasibility
influencing
factors
of
validating
eutopic
organoid
OE
as
in-vitro
models.
Eutopic
tissues
patients
were
selected
to
establish
organoids.
Morphologically,
organoids
showed
three-dimensional
glandular
structure
with
vacuoles
or
cystic
irregularities,
histological
features
endometriosis
well
preserved.
Immunofluorescence
positive
expression
markers
estrogen/progesterone
receptors.
Genetic
identification
revealed
100%
match
between
tissue,
indicating
common
origin.
The
effects
estrogen
progesterone
on
proliferation
secretion
differed
change
concentration.
successful
construction
provides
new
vitro
model
for
drug
intervention
mechanism
study
endometriosis.
Journal of Cellular and Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
29(6)
Published: March 1, 2025
ABSTRACT
Endometrium,
the
lining
of
uterus,
changes
dynamically
in
response
to
fluctuations
ovarian
hormones.
The
proper
endocrine
environment
regulates
endometrial
functions:
menstruation
and
supporting
pregnancy.
Obesity
is
closely
related
dysfunction,
which
seriously
affects
women's
health
fertility,
but
pathological
mechanism
unknown.
Chemerin
an
adipokine
involved
multiple
biological
events
such
as
immunity
metabolism
by
acting
on
its
functional
receptors.
This
study
aimed
characterise
effects
chemerin
human
epithelial
cells
RNA‐Seq.
12Z
were
utilised
model
because
immunoblot
results
showed
that
they
expressed
markers,
markers
receptors
for
chemerin.
Principal
component
analysis
(PCA)
treatment
significantly
altered
transcriptome.
Differential
Expression
Analysis
found
388
significant
differentially
genes
(DEG)
group
compared
with
controls.
Gene
Set
Enrichment
(GSEA)
inhibited
lipid
induced
epithelial‐mesenchymal
transition
(EMT)‐like
process
cellular
senescence.
More
importantly,
GSEA
immunoblots
restrained
STAT3
signalling
pathway,
required
receptivity
establishment.
Collectively,
these
findings
provide
new
evidence
over‐produced
underlying
dysfunctions
obesity.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(7), P. 3313 - 3313
Published: April 2, 2025
Ovarian
endometriosis
(OEM)
is
a
chronic
inflammatory
condition
that
impairs
ovarian
function.
While
its
effects
on
reserve
are
well
established,
the
long-term
consequences
of
OEM
dysfunction,
premature
failure
(POF),
and
systemic
health,
particularly
in
context
accelerated
aging,
remain
insufficiently
studied.
In
this
study,
we
employed
an
mouse
model
bulk
RNA
sequencing
to
investigate
underlying
mechanisms.
Our
results
show
accelerates
primordial
follicle
depletion
upregulates
mTOR
signaling
pathway
gene
expression,
along
with
mechanical
stress
paracrine
via
Hippo
Myc
pathways.
also
induces
irregular
estrus
fibrosis
aging
mice,
decreases
serum
AMH
levels,
increases
FSH
levels.
Systemically,
elevated
IgG
levels
contribute
osteoporosis
cognitive
decline,
both
linked
dysfunction
POF
OEM.
These
findings
elucidate
mechanisms
driving
highlight
broader
effects.
This
study
emphasizes
importance
monitoring
health
ectopic
tissue
safeguard
reserves
mitigate
risks
such
as
decline.
Reproductive BioMedicine Online,
Journal Year:
2025,
Volume and Issue:
50(4), P. 104785 - 104785
Published: April 1, 2025
The
endometrium
plays
a
crucial
role
in
female
health.
Globally,
millions
of
women
are
affected
by
endometrial/uterine
disorders,
yet
the
and
its
gynaecological
pathologies
have
been
understudied.
Gaining
insight
into
detailed
endometrial
architecture,
gene
expression,
spatial
temporal
cellular
interactions,
microenvironment
is
essential
for
understanding
physiology
pathophysiology
this
dynamic
tissue.
current
paper
highlights
latest
targets
advancing
research
that
include
single-cell
RNA
sequencing,
transcriptomics,
microbiome,
organoid
models,
analysis
menstrual
blood
less-studied
ageing.
authors
hope
summary
will
provide
more
novel
methods,
highlight
therapeutics
inspire
readers
to
generate
fresh
ideas
future
avenues.
Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
31(1)
Published: April 27, 2025
Abstract
Background
Endometriosis
can
lead
to
decreased
endometrial
receptivity,
reduced
rates
of
implantation,
and
diminished
ovarian
reserve.
Currently,
more
than
50%
infertile
women
are
found
suffer
from
endometriosis.
However
the
etiology
pathogenesis
endometriosis
still
poorly
understood.
Epithelial-mesenchymal
transition
(EMT)
has
been
confirmed
be
involved
in
PYK2
is
a
non-receptor
tyrosine
kinase
that
affects
cell
proliferation,
survival,
migration
by
regulating
intracellular
signaling
pathways.
plays
regulatory
role
EMT
process
affecting
expression
genes
associated
with
through
influence
transcription
factors.
Snail1
(Snail1)
key
highly
expressed
tissues.
On
other
hand,
invasive
metastatic
ability
cells
mainly
process.
However,
upstream
mechanisms
regulate
protein
stability
not
clear.
Methods
We
identified
kinase,
proline-rich
2
(PYK2
or
PTK2B),
examined
The
relevant
plasmids
were
constructed.
This
study
enrolled
20
patients
laparoscopically
meeting
ASRM
diagnostic
criteria,
collecting
ectopic
lesions
(14
endometriotic
cysts
6
deep
infiltrating
nodules)
along
matched
eutopic
tissues
(15
proliferative
phase,
5
secretory
phase)
as
controls.
All
tissue
specimens
underwent
immunohistochemical
analysis.
Human
stromal
(HESC)
isolated
normal
endometrium
3
control
for
vitro
meconium
induction.
Ectopic
(EESC)
obtained
lesions.
Protein
extracts
both
subjected
Western
blot
co-immunoprecipitation
(Co-IP)
interaction
validation.
Functional
assays
(proliferation/migration/invasion)
performed
using
EESC
11Z
lines
triplicate
biological
replicates.
Co-IP
experiments
verify
between
Snail1,
well
determine
specific
location
this
interaction.
Additionally,
we
effect
on
whether
VS-6063
inhibits
functions
cells.
models
established
five-week-old
female
C57BL/6
mice,
randomly
allocated
into
experimental
(
n
=
10)
groups.
Statistical
analyses
conducted
GraphPad
Prism
7.0,
employing
parametric
tests
normally
distributed
data
non-parametric
methods
otherwise,
Benjamini-Hochberg
correction
multiple
comparisons.
Results
It
acts
new
binding
partner
enhances
increasing
phosphorylation
Snail1.
promotes
migration,
invasion
while
inhibiting
decidualization.
demonstrated
inhibited
vitro,
growth
vivo.
Conclusions
novel
occurrence
development
up-regulating
which
could
promising
therapeutic
target
Proceedings of the National Academy of Sciences,
Journal Year:
2023,
Volume and Issue:
120(49)
Published: Nov. 29, 2023
The
uterus
is
vital
for
successful
reproduction
in
mammals,
and
two
different
types
of
epithelia
(luminal
glandular)
are
essential
embryo
implantation
pregnancy
establishment.
However,
the
cellular
molecular
factors
pathways
governing
postnatal
epithelium
maturation,
determination,
differentiation
developing
yet
to
be
elucidated.
Here,
neonatal
mouse
was
isolated
subjected
single-cell
transcriptome
(scRNA-seq)
analysis.
Both
undifferentiated
determined
luminal
were
heterogeneous
contained
several
cell
clusters
based
on
transcription
profiles.
Substantial
gene
expression
differences
evident
as
matured
differentiated
between
days
1
15.
Two
new
glandular
epithelium-expressed
genes
(
Gas6
Cited4
)
identified
validated
by
situ
hybridization.
Trajectory
analyses
provided
a
framework
understanding
lineage
bifurcation,
differentiation.
A
candidate
set
regulatory
networks
that
potentially
direct
specification
morphogenesis.
This
atlas
provides
foundation
important
discover
intrinsic
mechanisms
directing
uterine
morphogenesis
during
critical
window
development.