IntechOpen eBooks,
Год журнала:
2025,
Номер
unknown
Опубликована: Май 7, 2025
The
pandemic
era
has
underscored
an
urgent
demand
for
more
human-relevant
and
ethical
models
in
viral
research.
Animal
have
been
the
primary
method
studying
infection
dynamics,
immune
responses,
potential
treatments
decades.
However,
their
limitations
accurately
simulating
human-specific
responses
raise
critical
questions
about
effectiveness
of
these
predicting
human
disease
outcomes.
Organoids—three-dimensional,
stem
cell-derived
structures
replicating
tissues’
architecture
functionality—present
a
groundbreaking
alternative.
This
review
examines
transformative
organoids
to
replace
animal
virology,
particularly
under
conditions
that
require
rapid,
precise,
ethically
sound
approaches.
With
ability
closely
mimic
tissue
environments,
enable
accurate
analysis
virus-host
interactions
predictive
drug
screening.
Beyond
advancing
scientific
precision,
significantly
reduce
concerns
logistical
challenges
associated
with
testing.
As
virology
field
pivots
toward
innovative,
human-centered
models,
stand
redefine
research
approaches,
promising
new
can
accelerate
development
effective
preventive
strategies
face
future
pandemics.
Infections
at
the
maternal-fetal
interface
can
directly
harm
fetus
and
induce
complications
that
adversely
impact
pregnancy
outcomes.
Innate
immune
signaling
by
both
fetal-derived
placental
trophoblasts
maternal
decidua
must
provide
antimicrobial
defenses
this
critical
without
compromising
its
integrity.
Here,
we
developed
matched
trophoblast
(TO)
organoids
(DO)
from
human
placentas
to
define
relative
contributions
of
these
cells
antiviral
interface.
We
demonstrate
TO
DO
basally
secrete
distinct
immunomodulatory
factors,
including
constitutive
release
type
III
interferon
IFN-λ2
TOs,
differentially
respond
viral
infections
through
induction
organoid-specific
factors.
Finally,
differential
susceptibility
innate
cytomegalovirus
(HCMV)
develop
a
co-culture
model
which
showed
trophoblast-derived
factors
protect
decidual
HCMV
infection.
Our
findings
establish
as
ex
vivo
models
study
vertically
transmitted
highlight
differences
in
decidua.
The Innovation,
Год журнала:
2024,
Номер
5(3), С. 100620 - 100620
Опубликована: Апрель 1, 2024
In
the
last
decade,
organoid
research
has
entered
a
golden
era,
signifying
pivotal
shift
in
biomedical
landscape.
The
year
2023
marked
milestone
with
publication
of
thousands
papers
this
arena,
reflecting
exponential
growth.
However,
amid
burgeoning
expansion,
comprehensive
and
accurate
overview
field
been
conspicuously
absent.
Our
review
is
intended
to
bridge
gap,
providing
panoramic
view
rapidly
evolving
We
meticulously
analyze
from
eight
distinctive
vantage
points,
harnessing
our
rich
experience
academic
research,
industrial
application,
clinical
practice.
present
deep
exploration
advances
technology,
underpinned
by
long-standing
involvement
arena.
narrative
traverses
historical
genesis
organoids
their
transformative
impact
across
various
sectors,
including
oncology,
toxicology,
drug
development.
delve
into
synergy
between
avant-garde
technologies
such
as
synthetic
biology
single-cell
omics
discuss
role
tailoring
personalized
medicine,
enhancing
high-throughput
screening,
constructing
physiologically
pertinent
disease
models.
analysis
reflective
discourse
provide
dive
existing
landscape
emerging
trends
technology.
spotlight
technological
innovations,
methodological
evolution,
broadening
spectrum
applications,
emphasizing
revolutionary
influence
discovery,
other
fields.
Looking
ahead,
we
cautiously
anticipate
future
developments
especially
its
potential
implications
for
patient
care,
new
avenues
research.
trust
that
will
be
an
asset
researchers,
clinicians,
patients
keen
interest
medical
strategies.
offer
broad
prospective
capabilities
encompassing
wide
range
current
applications.
summary,
attempt
field.
reflections,
summaries,
projections
might
useful
researchers
hope
contribute
shaping
trajectory
dynamic
advancing
Cell Death Discovery,
Год журнала:
2023,
Номер
9(1)
Опубликована: Окт. 10, 2023
As
an
essential
component
of
the
maternal-fetal
interface,
placental
syncytiotrophoblast
layer
contributes
to
a
successful
pregnancy
by
secreting
hormones
necessary
for
pregnancy,
transporting
nutrients,
mediating
gas
exchange,
balancing
immune
tolerance,
and
resisting
pathogen
infection.
Notably,
deficiency
in
mononuclear
trophoblast
cells
fusing
into
multinucleated
has
been
linked
adverse
outcomes,
such
as
preeclampsia,
fetal
growth
restriction,
preterm
birth,
stillbirth.
Despite
availability
many
models
study
fusion,
there
exists
notable
disparity
from
ideal
model,
limiting
deeper
exploration
development.
Here,
we
reviewed
existing
employed
investigation
human
fusion
several
aspects,
including
development
history,
latest
progress,
advantages,
disadvantages,
scope
application,
challenges.
The
literature
searched
covers
monolayer
cell
lines,
primary
trophoblast,
explants,
stem
cells,
pluripotent
three-dimensional
spheres,
organoids,
placenta-on-a-chip
1938
2023.
These
diverse
have
significantly
enhanced
our
comprehension
regulation
underlying
mechanisms
placental-related
disorders.
Through
this
review,
objective
is
provide
readers
with
thorough
understanding
models,
making
it
easier
select
most
suitable
address
specific
experimental
requirements
or
scientific
inquiries.
Establishment
application
models.
Journal of Cell Science,
Год журнала:
2023,
Номер
137(5)
Опубликована: Сен. 7, 2023
Human
trophoblast
organoids
(TOs)
are
a
three-dimensional
ex
vivo
culture
model
that
can
be
used
to
study
various
aspects
of
placental
development,
physiology
and
pathology.
However,
standard
culturing
TOs
does
not
recapitulate
the
cellular
orientation
chorionic
villi
in
given
multi-nucleated
syncytiotrophoblast
(STB)
develops
largely
within
inner
facing
surfaces
these
(STBin).
Here,
we
developed
method
under
conditions
vivo.
We
show
STBin
suspension
with
gentle
agitation
leads
development
containing
STB
on
outer
surface
(STBout).
Using
membrane
capacitance
measurements,
determined
outermost
STBout
contain
large
syncytia
comprising
>50
nuclei,
whereas
small
(<10
nuclei)
mononuclear
cells.
The
growth
mimic
thus
allows
for
variety
biology
physiological
conditions.
Frontiers in Microbiology,
Год журнала:
2021,
Номер
12
Опубликована: Ноя. 11, 2021
Malaria
remains
a
global
health
burden
with
Plasmodium
falciparum
accounting
for
the
highest
mortality
and
morbidity.
in
pregnancy
can
lead
to
development
of
placental
malaria,
where
P.
-infected
erythrocytes
adhere
receptors,
triggering
inflammation
subsequent
damage,
causing
harm
both
mother
her
infant.
Histopathological
studies
placentas
revealed
various
abnormalities
such
as
excessive
perivillous
fibrinoid
deposits,
breakdown
syncytiotrophoblast
integrity,
trophoblast
basal
lamina
thickening,
increased
syncytial
knotting,
accumulation
mononuclear
immune
cells
within
intervillous
spaces.
These
events
turn,
are
likely
impair
function,
ultimately
insufficiency,
intrauterine
growth
restriction,
preterm
delivery
low
birth
weight.
Hence,
better
understanding
mechanisms
behind
alterations
damage
during
malaria
is
needed
design
effective
interventions.
In
this
review,
using
evidence
from
human
murine
models,
an
integrated
view
on
potential
underlying
pathologies
provided.
The
molecular,
immunological
metabolic
changes
infected
that
reflect
their
responses
parasitic
infection
injury
discussed.
Finally,
models
be
used
by
researchers
improve
our
pathogenesis
presented.
TMEM16F,
a
Ca
2+
-activated
phospholipid
scramblase
(CaPLSase),
is
critical
for
placental
trophoblast
syncytialization,
HIV
infection,
and
SARS-CoV2-mediated
however,
how
TMEM16F
activated
during
cell
fusion
unclear.
Here,
using
trophoblasts
as
model
fusion,
we
demonstrate
that
influx
through
the
permeable
transient
receptor
potential
vanilloid
channel
TRPV4
activation
plays
role
in
subsequent
human
fusion.
GSK1016790A,
specific
agonist,
robustly
activates
trophoblasts.
We
also
show
are
functionally
coupled
within
microdomains
line
patch-clamp
electrophysiology.
Pharmacological
inhibition
or
gene
silencing
of
hinders
syncytialization.
Our
study
uncovers
functional
expression
one
physiological
mechanisms
trophoblasts,
thus
providing
us
with
novel
strategies
to
regulate
CaPLSase
activity
checkpoint
physiologically
disease-relevant
events.
Cell Reports,
Год журнала:
2024,
Номер
43(2), С. 113698 - 113698
Опубликована: Янв. 23, 2024
Congenital
cytomegalovirus
(cCMV)
is
the
most
common
intrauterine
infection,
leading
to
infant
neurodevelopmental
disabilities.
An
improved
knowledge
of
correlates
protection
against
cCMV
needed
guide
prevention
strategies.
Here,
we
employ
an
ex
vivo
model
human
CMV
(HCMV)
infection
in
decidual
tissues
women
with
and
without
preconception
immunity
CMV,
recapitulating
nonprimary
vs.
primary
at
authentic
maternofetal
transmission
site.
We
show
that
exhibit
intrinsic
resistance
HCMV,
mounting
a
rapid
activation
tissue-resident
memory
CD8
Cell Systems,
Год журнала:
2024,
Номер
15(5), С. 425 - 444.e9
Опубликована: Май 1, 2024
The
placenta
is
a
selective
maternal-fetal
barrier
that
provides
nourishment
and
protection
from
infections.
However,
certain
pathogens
can
attach
to
even
cross
the
placenta,
causing
pregnancy
complications
with
potential
lifelong
impacts
on
child's
health.
Here,
we
profiled
at
single-cell
level
placental
responses
three
associated
intrauterine
complications—Plasmodium
falciparum,
Listeria
monocytogenes,
Toxoplasma
gondii.
We
found
upon
exposure
pathogens,
all
lineages
trigger
inflammatory
may
compromise
function.
Additionally,
characterized
of
fetal
macrophages
known
as
Hofbauer
cells
(HBCs)
each
pathogen
propose
they
are
probable
niche
for
T.
Finally,
revealed
how
P.
falciparum
adapts
microenvironment
by
modulating
protein
export
into
host
erythrocyte
nutrient
uptake
pathways.
Altogether,
have
defined
cellular
networks
signaling
pathways
mediating
acute
could
contribute
complications.
Cellular and Molecular Immunology,
Год журнала:
2024,
Номер
21(9), С. 959 - 981
Опубликована: Авг. 12, 2024
Abstract
Cytomegalovirus
(CMV),
a
representative
member
of
the
Betaherpesvirinae
subfamily
herpesviruses,
is
common
in
human
population,
but
immunocompetent
individuals
are
generally
asymptomatic
when
infected
with
this
virus.
However,
immunocompromised
and
immunologically
immature
fetuses
newborns,
CMV
can
cause
wide
range
often
long-lasting
morbidities
even
death.
not
only
widespread
throughout
population
it
also
its
hosts,
infecting
establishing
latency
nearly
all
tissues
organs.
Thus,
understanding
pathogenesis
immune
responses
to
virus
prerequisite
for
developing
effective
prevention
treatment
strategies.
Multiple
arms
system
engaged
contain
infection,
general
concepts
control
now
reasonably
well
understood.
Nonetheless,
recent
years,
tissue-specific
have
emerged
as
an
essential
factor
resolving
infection.
As
differ
biology
function,
so
do
pathological
processes
during
This
review
discusses
state-of-the-art
knowledge
response
infection
tissues,
particular
emphasis
on
several
well-studied
most
commonly
affected