IntechOpen eBooks,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 16, 2024
Spermatogonial
stem
cells
(SSCs)
play
a
pivotal
role
in
male
germ
cell
development
and
are
essential
for
the
continuous
production
of
spermatozoa
throughout
male’s
reproductive
life.
The
regulation
gene
expression
SSCs
is
highly
intricate
process
crucial
maintaining
spermatogenesis.
Long
noncoding
RNAs
(lncRNAs)
have
emerged
as
significant
players
epigenetic
transcriptional
expression.
This
abstract
provides
an
overview
current
state
knowledge
regarding
involvement
lncRNAs
spermatogonial
explores
potential
therapeutic
applications
associated
with
targeting
context
infertility
health.
review
delves
into
mechanisms
by
which
influence
SSCs,
including
their
chromatin
remodeling,
regulation,
post-transcriptional
modifications.
network
interactions
between
protein-coding
genes
highlighted,
showcasing
impact
on
delicate
balance
required
SSC
self-renewal
differentiation.
Furthermore,
interventions
treatment
disorders
discussed,
offering
insight
future
directions
research
this
field.
Frontiers in Cell and Developmental Biology,
Год журнала:
2024,
Номер
11
Опубликована: Фев. 13, 2024
This
manuscript
comprehensively
reviews
the
interrelationship
between
spermatogonial
stem
cells
(SSCs)
and
JAK/STAT
signaling
pathway.
Spermatogonial
in
testes
of
male
mammals,
characterized
by
their
self-renewal
pluripotential
differentiation
capabilities,
are
essential
for
tissue
regeneration,
immunomodulation,
advancements
regenerative
medicine.
review
delves
into
historical
background
biological
characteristics
SSCs,
with
a
particular
emphasis
on
pivotal
role
pathway
proliferation,
maturation,
processes.
Research
indicates
that
extensively
influences
various
functionalities
cells,
encompassing
differentiation,
homing,
adaptation
to
microenvironment.
Herein,
we
collate
dissect
related
studies,
shedding
light
intricate
dynamics
SSCs
pathway,
examine
implications
these
interactions
attributes
SSCs.
Furthermore,
discusses
profound
findings
preclinical
research
domain
cellular
engineering.
It
is
acknowledged
that,
despite
investigations
humans
larger
mammals
remain
inadequate,
necessitating
more
in-depth
exploration
establish
comprehensive
theoretical
framework.
Overall,
this
offers
an
invaluable
reference
deciphering
mechanisms
cell
pathways
establishes
groundwork
research.
Abstract
Background
The
issue
of
male
fertility
is
becoming
increasingly
common
due
to
genetic
differences
inherited
over
generations.
Gene
expression
and
evaluation
non-coding
RNA
(ncRNA),
crucial
for
sperm
development,
are
significant
factors.
This
gene
can
affect
motility
and,
consequently,
fertility.
Understanding
the
intricate
protein
interactions
that
play
essential
roles
in
differentiation
development
vital.
knowledge
could
lead
more
effective
treatments
interventions
infertility.
Materials
methods
Our
research
aim
identify
new
key
genes
ncRNA
involved
non-obstructive
azoospermia
(NOA),
improving
diagnosis
offering
accurate
estimates
successful
extraction
based
on
an
individual’s
genotype.
Results
We
analyzed
transcript
three
NOA
patients
who
tested
negative
issues,
employing
comprehensive
genome-wide
analysis
approximately
50,000
sequences
using
microarray
technology.
compared
profiles
between
normal
sperm.
found
differences:
150
were
up-regulated,
78
down-regulated,
along
with
24
ncRNAs
up-regulated
13
down-regulated
conditions.
By
cross-referencing
our
results
a
single-cell
genomics
database,
we
identified
overexpressed
biological
process
terms
differentially
expressed
genes,
such
as
“protein
localization
endosomes”
“xenobiotic
transport.”
Overrepresented
molecular
function
included
“voltage-gated
calcium
channel
activity,”
“growth
hormone-releasing
hormone
receptor
“sialic
acid
transmembrane
transporter
activity.”
Analysis
revealed
nine
hub
associated
sperm:
RPL34,
CYB5B,
GOL6A6,
LSM1,
ARL4A,
DHX57,
STARD9,
HSP90B1
,
VPS36
.
Conclusions
These
their
interacting
proteins
may
role
pathophysiology
germ
cell
abnormalities
DNA and Cell Biology,
Год журнала:
2023,
Номер
42(10), С. 617 - 637
Опубликована: Авг. 23, 2023
Recent
studies
have
shown
that
several
members
of
the
G-protein-coupled
receptors
(GPCR)
superfamily
play
crucial
roles
in
maintenance
ion-water
homeostasis
sperm
and
Sertoli
cells,
development
germ
formation
blood
barrier,
maturation
sperm.
The
GPCR,
guanyl-nucleotide
exchange
factor,
membrane
traffic
protein,
small
GTPase
genes
were
analyzed
by
microarray
bioinformatics
(3513
cell
genes).
In
analyses
three
human
cases
with
different
nonobstructive
azoospermia
sperm,
expression
GOLGA8IP,
OR2AT4,
PHKA1,
A2M,
OR56A1,
SEMA3G,
LRRC17,
APP,
ARHGAP33,
RABGEF1,
NPY2R,
GHRHR,
LTB4R2,
GRIK5,
OR6K6,
NAPG,
OR6C65,
VPS35,
FPR3,
ARL4A
was
upregulated,
while
MARS,
SIRPG,
OGFR,
GPR150,
LRRK1,
NGEF
downregulated.
There
an
increase
GBP3,
TNF,
TGFB3,
CLTC
cells
NOA,
whereas
PAQR4,
RRAGD,
RAC2,
SERPINB8,
IRPB1,
MRGPRF,
RASA2,
RGS2,
RAP2A,
RAB2B,
ARL17,
SERINC4,
XIAP,
DENND4C,
ANKRA2,
CSTA,
STX18,
SNAP23
A
combined
analysis
Enrich
Shiny
Gene
Ontology
(GO),
STRING,
Cytoscape
used
to
predict
proteins'
molecular
interactions
then
recognize
master
pathways.
Functional
enrichment
showed
biological
process
(BP),
regulation
protein
metabolic
process,
GTPase-mediated
signal
transduction
significantly
expressed
up-/downregulated
differentially
(DEGs)
function
(MF)
experiments
DEGs
up-/downregulated,
it
found
GPCR
activity,
guanyl
ribonucleotide
binding,
activity
nucleoside-triphosphatase
overexpressed.
An
GO
findings
BP
MF
be
common
DEGs.
When
these
gene
mutations
been
validated,
they
can
create
new
antagonists
or
agonists
are
receptor-selective.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Авг. 27, 2024
Our
study
probed
the
differences
in
ion
channel
gene
expression
endometrium
of
women
with
Recurrent
Implantation
Failure
(RIF)
compared
to
fertile
women.
We
analyzed
relative
genes
coding
for
T-type
Ca2+,
ENaC,
CFTR,
and
KCNQ1
channels
endometrial
samples
from
20
RIF-affected
10
control
women,
aged
22-35,
via
microarray
analysis
quantitative
real-time
PCR.
Additionally,
we
examined
DNA
methylation
regulatory
region
using
ChIP
The
bioinformatics
component
our
research
included
Gene
Ontology
analysis,
protein-protein
interaction
networks,
signaling
pathway
mapping
identify
key
biological
processes
pathways
implicated
RIF.
This
led
discovery
significant
alterations
RIF
women's
endometrium,
most
notably
an
overexpression
CFTR
reduced
SCNN1A,
SCNN1B,
SCNN1G,
CACNA1H,
KCNQ1.
A
higher
level
KCNQ1's
was
also
observed
patients.
Gene-set
enrichment
highlighted
a
presence
involved
transport
membrane
potential
regulation,
particularly
sodium
calcium
complexes,
which
are
vital
cation
movement
across
cell
membranes.
Genes
were
enriched
broader
transmembrane
transporter
underscoring
their
extensive
role
cellular
homeostasis
signaling.
These
findings
suggest
involvement
pathology
implantation
failure,
offering
new
insights
into
mechanisms
behind
possible
therapeutic
targets.
Prostate
cancer
(PCa)
is
the
second
most
common
malignant
neoplasm
in
males
and
fifth
leading
cause
of
cancer-related
mortality.
Due
to
use
prostate-specific
antigen
(PSA)
screening
improved
biopsy
techniques,
persons
identified
with
early-stage
prostate
often
have
a
positive
prognosis
after
comprehensive
treatment.
Nonetheless,
latent
illness
that
may
present
as
an
asymptomatic
tumor
individuals
aged
20-30.
The
overall
survival
(OS)
men
advanced
PCa
significantly
diminished.
Consequently,
there
immediate
want
for
innovative,
accurate
biomarkers
detect
early
cancer.
This
research
analyzed
interaction
network
differentially
expressed
genes
(DEGs)
related
metabolite
interconversion
enzymes
by
gene
expression
microarray
data,
single-cell
RNA
sequencing,
oncogenes,
suppressor
(TSGs)
utilizing
bioinformatics
techniques.
kind
analysis
has
not
been
documented
prior
studies.
We
then
used
dataset
acquired
Cancer
Genome
Atlas
(TCGA)
confirm
our
findings.
Genes
including
CYP3A5,
PDE8B,
AOX1,
BNIPL,
FADS2,
RRM2,
ALDH3B2,
GSTM2
be
significant
diagnosis
treatment
PCa.
Our
objective
was
provide
new
perspectives
on
molecular
properties
pathways
DEGs
uncover
potential
play
crucial
role
genesis
progression
Biology,
Год журнала:
2025,
Номер
14(4), С. 387 - 387
Опубликована: Апрель 8, 2025
Histone
modifications
play
a
critical
role
in
regulating
gene
expression
and
maintaining
the
functionality
of
spermatogonial
stem
cells
(SSCs),
which
are
essential
for
male
fertility
spermatogenesis.
In
this
study,
we
integrated
microarray
single-cell
RNA-sequencing
(scRNA-seq)
data
to
identify
key
histone
modification
changes
associated
with
SSC
function
aging.
Through
differential
analysis,
identified
2509
differentially
expressed
genes
(DEGs)
SSCs
compared
fibroblasts.
Among
these,
involved
modification,
such
as
KDM5B,
SCML2,
SIN3A,
ASXL3,
were
highlighted
their
significant
roles
chromatin
remodeling
regulation.
Protein–protein
interaction
(PPI)
networks
ontology
(GO)
enrichment
analysis
revealed
biological
processes
organization,
demethylation,
chromosome
structure
maintenance.
Weighted
co-expression
network
(WGCNA)
further
three
modules
co-expressed
related
Additionally,
ligand–receptor
scoring
based
on
tumor
microenvironment
suggested
potential
signaling
pathways
that
could
influence
stemness
differentiation
SSCs.
Our
findings
provide
new
insights
into
molecular
mechanisms
underlying
aging,
highlighting
therapeutic
targets
preserving
improving
SSC-culturing
techniques.
This
study
advances
our
understanding
biology
will
serve
valuable
resource
future
investigations
preservation.
Genomics,
Год журнала:
2025,
Номер
117(3), С. 111046 - 111046
Опубликована: Апрель 23, 2025
Non-obstructive
azoospermia
(NOA)
is
a
severe
form
of
male
infertility,
yet
its
underlying
molecular
mechanisms
remain
poorly
understood.
This
study
aimed
to
identify
key
regulatory
non-coding
RNAs
(ncRNAs)
and
hub
genes
associated
with
NOA
through
an
integrative
bioinformatics
approach.
Using
microarray
analysis,
we
examined
4956
ncRNAs
identified
29
differentially
expressed
(14
upregulated,
15
downregulated)
in
compared
healthy
individuals.
Co-expression
analysis
revealed
significant
interactions
between
lncRNAs,
miRNAs,
mRNAs,
predicting
31
target
mRNAs
within
the
network.
Further,
single-cell
transcriptomic
four
pivotal
Sertoli
cells:
CLTC,
XIAP,
DHFR
(upregulated)
STMN1
(downregulated).
Functional
enrichment
highlighted
critical
pathways,
including
mitotic
spindle
organization
phosphatase
activity,
suggesting
their
involvement
pathophysiology.
Our
findings
provide
novel
insights
into
propose
potential
biomarkers
for
improved
diagnosis
therapeutic
strategies.