Cell and Tissue Journal,
Год журнала:
2023,
Номер
14(2), С. 153 - 165
Опубликована: Июнь 22, 2023
هدف:
در
این
تحقیق،
ما
به
بیان
PLZF
و
VASA
لولههای
اسپرم
ساز
سلولهای
زایای
in
vivo
vitro
نگاه
کردیم.
مواد
روشها:
جداسازی
سلول
های
بنیادی
اسپرماتوگونیال،
ایمونوهیستوشیمی
(IHC)،
ایمونوسیتوشیمی
(ICC)
واکنش
زنجیره
ای
پلیمراز
رونوشت
معکوس
Fluidigm
(RT-PCR)
برای
تجزیه
تحلیل
بافت
بیضه
موش
استفاده
شد.
نتایج:
مطالعه
تجربی،
حالیکه
اسپرماتوگونیال
تمایز
نیافته
شدت
را
میکنند،
سایر
زاینده
واقع
لوله
نشانگر
منفی
بودند.
از
سوی
دیگر،
زایا
نزدیک
غشای
پایه
لولههای
نشان
دادند
ICC
بیانگر
بالاتر
سلولهای
جدا
شده
مقایسه
با
یافته
بود.
نتایج
RT-PCR
بلادرنگ
معنیداری
(05/0
Scientific Reports,
Год журнала:
2022,
Номер
12(1)
Опубликована: Окт. 14, 2022
Abstract
VASA,
also
known
as
DDX4,
is
a
member
of
the
DEAD-box
proteins
and
an
RNA
binding
protein
with
ATP-dependent
helicase.
The
VASA
gene
expression,
which
required
for
human
germ
cell
development,
may
lead
to
infertility.
Immunocytochemistry
immunohistochemistry
were
used
examine
expression
in
testis
sections
azoospermic
patients,
in-vitro
in-silico
models.
Some
studies
fertile
humans
showed
basal
adluminal
compartments
seminiferous
tubules.
Our
infertile
luminal
tubule.
immunohistochemical
analysis
three
cases
different
levels
non-obstructive
azoospermia
revealed
higher
VASA-positive
cells.
For
this
purpose,
Enrichr
Shiny
Gene
Ontology
databases
pathway
enrichment
ontology.
STRING
Cytoscape
online
evaluation
applied
predict
proteins'
functional
molecular
interactions
performed
recognize
master
genes,
respectively.
According
obtained
results,
main
functions
up-regulated
downregulated
genes
include
meiotic
cycle,
binding,
differentiation.
analyses
presented
seven
i.e.,
DDX5,
TNP2,
DDX3Y,
TDRD6,
SOHL2,
DDX31,
SYCP3,
hub
involved
infertility
co-function
protein–protein
interaction.
findings
suggest
that
its
interacting
could
help
determine
pathophysiology
abnormalities
International Journal of Molecular Sciences,
Год журнала:
2022,
Номер
23(20), С. 12570 - 12570
Опубликована: Окт. 20, 2022
Non-obstructive
azoospermia
(NOA)
is
a
serious
cause
of
male
infertility.
The
Sertoli
cell
responds
to
androgens
and
takes
on
roles
supporting
spermatogenesis,
which
may
This
work
aims
enhance
the
genetic
diagnosis
NOA
via
discovery
new
hub
genes
implicated
in
human
better
assess
odds
successful
sperm
extraction
according
individual's
genotype.
Whole
exome
sequencing
(WES)
was
done
three
patients
find
key
involved
NOA.
We
evaluated
genome-wide
transcripts
(about
50,000
transcripts)
by
microarray
between
non-obstructive
normal
cells.
analysis
cases
with
different
revealed
that
32
were
upregulated,
expressions
113
downregulated
versus
case.
For
this
purpose,
Enrich
Shiny
GO,
STRING,
Cytoscape
online
evaluations
applied
predict
functional
molecular
interactions
proteins
then
recognize
master
pathways.
enrichment
demonstrated
biological
process
(BP)
terms
"inositol
lipid-mediated
signaling",
"positive
regulation
transcription
RNA
polymerase
II",
DNA-templated
transcription"
significantly
changed
upregulated
differentially
expressed
(DEGs).
BP
investigation
DEGs
highlighted
"mitotic
cytokinesis",
"regulation
protein-containing
complex
assembly",
"cytoskeleton-dependent
"peptide
metabolic
process".
Overrepresented
function
(MF)
included
"ubiquitin-specific
protease
binding",
"protease
"phosphatidylinositol
trisphosphate
phosphatase
activity",
"clathrin
light
chain
binding".
Interestingly,
MF
overexpression
"ATPase
inhibitor
"glutathione
transferase
regulator
activity".
Our
findings
suggest
these
their
interacting
could
help
determine
pathophysiologies
germ
abnormalities
Cell Biochemistry and Function,
Год журнала:
2023,
Номер
41(7), С. 767 - 778
Опубликована: Авг. 16, 2023
Abstract
Noncoding
RNAs
(ncRNAs)
are
active
regulators
of
a
wide
range
biological
and
physiological
processes,
including
the
majority
mammalian
reproductive
events.
Knowledge
activities
ncRNAs
in
context
reproduction
will
allow
for
more
comprehensive
comparative
understanding
male
sterility
fertility.
In
this
review,
we
describe
recent
advances
ncRNA‐mediated
control
emphasize
importance
several
aspects
reproduction,
such
as
germ
cell
biogenesis
organ
activity.
Furthermore,
focus
on
gene
expression
regulatory
feedback
loops
hormones
ncRNA
to
better
understand
commitment
function.
Finally,
study
shows
role
failure
provides
suggestions
further
research.
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