European Surgical Research,
Год журнала:
2024,
Номер
65(1), С. 137 - 145
Опубликована: Окт. 29, 2024
Background:
Normothermic
machine
perfusion
(NMP)
is
gradually
being
introduced
into
clinical
transplantation
to
improve
the
quality
of
organs
and
increase
utilisation.
This
review
details
current
understanding
underlying
mechanistic
effects
NMP
in
heart,
lung,
liver,
kidney.
It
also
considers
recent
advancements
extend
interval
these
use
introduce
novel
therapeutic
interventions,
with
a
focus
on
organ
modulation.
Summary:
The
re-establishment
circulation
during
leads
upregulation
inflammatory
immune
mediators,
similar
an
ischaemia-reperfusion
injury
response.
level
determined
by
condition
organ,
but
inflammation
may
be
exacerbated
passenger
leucocytes
that
emerge
from
perfusion.
There
evidence
damaged
can
recover
prolonged
advantageous.
In
successful
7-day
has
been
achieved.
delivery
agents
aid
repair
used
modify
reduce
immunogenicity
or
change
structure
blood
group
antigens
create
universal
donor
organ.
Key
Messages:
application
growing
area
research
increasingly
clinic.
future,
offer
opportunity
practice.
If
preserved
for
days
system,
become
elective
rather
than
emergency
procedure.
ability
therapies
effective
way
treat
avoid
complexity
treating
recipient.
Over
the
last
50
years,
liver
transplantation
has
evolved
into
a
procedure
routinely
performed
in
many
countries
worldwide.
Those
able
to
access
this
therapy
frequently
experience
miraculous
risk-benefit
ratio,
particularly
if
they
face
imminently
life-threatening
disease.
decades,
success
of
transplantation,
with
dramatic
improvements
early
posttransplant
survival,
aggressively
driven
demand.
However,
despite
emergence
living
donors
augment
deceased
as
source
organs,
supply
lagged
far
behind
As
result,
rationing
been
an
unfortunate
focus
recent
decades.
Recent
shifts
epidemiology
disease
combined
transformative
innovations
preservation
suggest
that
underlying
premise
organ
shortage
may
erode
foreseeable
future.
The
will
sharpen
on
improving
equitable
while
mitigating
constraints
related
workforce
training,
infrastructure
for
recovery
and
rehabilitation,
their
associated
costs.
Research
efforts
undoubtedly
blossom
aim
optimizing
both
timing
conditions
transplantation.
Coupled
advances
genetic
engineering,
regenerative
biology,
cellular
therapies,
portfolio
innovation,
broad
deep,
offers
promise
that,
future,
not
only
be
broadly
available
those
need
but
also
represent
highly
durable
life-saving
therapy.
International Journal of Medical Sciences,
Год журнала:
2025,
Номер
22(3), С. 528 - 550
Опубликована: Янв. 1, 2025
Background:
Worldwide,
approximately
1.7
billion
people
are
afflicted
with
musculoskeletal
(MSK)
diseases,
posing
significant
health
challenges.
The
introduction
of
single-cell
RNA
sequencing
(scRNA-seq)
technology
provides
novel
insights
and
approaches
to
comprehend
the
onset,
progression,
treatment
MSK
diseases.
Nevertheless,
there
is
a
remarkable
lack
analytical
descriptive
studies
regarding
trajectory,
essential
research
directions,
current
situation,
pivotal
focuses,
upcoming
perspectives.
Therefore,
aim
this
present
comprehensive
overview
advancements
made
in
scRNA-seq
for
disorders
over
past
15
years.
Methods:
It
utilizes
robust
dataset
derived
from
Web
Science
Core
Collection,
encompassing
January
1,
2009,
through
September
6,
2024.
To
achieve
this,
advanced
methodologies
were
applied
conduct
thorough
scientometric
visual
analyses.
Results:
findings
underscore
preeminent
role
China,
which
contributes
63.49%
total
publications,
thereby
exerting
substantial
impact
within
domain.
Notable
contributions
came
institutions
such
as
Shanghai
Jiao
Tong
University,
Sun
Yat-sen
Harvard
Medical
School,
Liu
Yun
being
leading
contributor.
Frontiers
Immunology
published
greatest
number
papers
field.
This
study
identified
joint
bone
neoplasms,
fractures,
intervertebral
disc
degeneration
main
focuses.
Conclusion:
extensive
analysis
benefits
both
experienced
novice
researchers
by
facilitating
immediate
access
critical
data,
fostering
innovation
Heliyon,
Год журнала:
2024,
Номер
10(7), С. e28358 - e28358
Опубликована: Март 19, 2024
The
development
of
single-cell
omics
tools
has
enabled
scientists
to
study
the
tumor
microenvironment
(TME)
in
unprecedented
detail.
However,
each
different
techniques
may
have
its
unique
strengths
and
limitations.
Here
we
directly
compared
two
commercially
available
high-throughput
RNA
sequencing
(scRNA-seq)
technologies
-
droplet-based
10X
Chromium
Journal of Experimental Botany,
Год журнала:
2024,
Номер
75(17), С. 5188 - 5203
Опубликована: Март 11, 2024
Biotic
and
abiotic
environmental
cues
are
major
factors
influencing
plant
growth
productivity.
Interactions
with
biotic
(e.g.
symbionts
pathogens)
changes
in
temperature,
water,
or
nutrient
availability)
trigger
signaling
downstream
transcriptome
adjustments
plants.
While
bulk
RNA-sequencing
technologies
have
traditionally
been
used
to
profile
these
transcriptional
changes,
tissue
homogenization
may
mask
heterogeneity
of
responses
resulting
from
the
cellular
complexity
organs.
Thus,
whether
different
cell
types
respond
equally
fluctuations,
subsets
cell-type
specific,
long-lasting
questions
biology.
The
recent
breakthrough
single-cell
transcriptomics
research
offers
an
unprecedented
view
under
changing
conditions.
In
this
review,
we
discuss
contribution
understanding
cell-type-specific
interactions.
Besides
biological
findings,
present
some
technical
challenges
coupled
studies
plant-environment
interactions,
proposing
possible
solutions
exciting
paths
for
future
research.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Ноя. 30, 2023
Normothermic
machine
perfusion
(NMP)
after
static
cold
storage
is
increasingly
used
for
preservation
and
assessment
of
human
donor
livers
prior
to
transplantation.
Biliary
viability
during
NMP
reduces
the
risk
post-transplant
biliary
complications.
However,
understanding
molecular
changes
in
system
remains
incomplete.
We
performed
an
in-depth,
unbiased
proteomics
analysis
bile
collected
sequential
hypothermic
perfusion,
rewarming
55
livers.
Longitudinal
reveals
proteins
reflective
cellular
damage
at
early
stages,
followed
by
upregulation
secretory
immune
response
processes.
Livers
with
chemistry
acceptable
transplantation
reveal
protein
patterns
implicated
regenerative
processes,
including
proliferation,
compared
inadequate
chemistry.
These
findings
are
reinforced
detection
gene
transcripts
liver
tissue
before
perfusion.
Our
comprehensive
transcriptomics
data
sets
provide
potential
further
evaluate
mechanisms
refine
criteria.
Abstract
Liver
fibrosis
can
cause
hepatitis
B
virus
(HBV)‐associated
hepatocellular
carcinoma.
Menstrual
blood‐derived
mesenchymal
stem
cells
(MenSCs)
ameliorate
liver
through
paracrine.
Single‐cell
RNA
sequencing
(scRNA‐seq)
may
be
used
to
explore
the
roadmap
of
activated
hepatic
stellate
cell
(aHSC)
inactivation
target
fibrosis.
This
study
established
HBV
transgenic
(HBV‐Tg)
mouse
model
carbon
tetrachloride
(CCl
4
)‐induced
and
demonstrated
that
MenSCs
migrated
injured
improve
serological
indices
reduce
fibrotic
accumulation.
RNA‐bulk
analysis
revealed
mediated
extracellular
matrix
accumulation
adhesion.
parenchymal
nonparenchymal
were
identified
by
scRNA‐seq
in
control,
CCl
,
MenSC
groups,
revealing
heterogeneity
fibroblasts/HSCs.
A
CellChat
diminished
intercellular
adhesion
molecule
(ICAM)
signaling
is
vital
for
therapy.
Specifically,
Icam1
aHSCs
acted
on
Itgal
/
Itgb2
Itgam
neutrophils,
causing
decreased
The
expression
was
higher
group
than
control
after
therapy
neutrophil
clusters.
Lcn2
Pglyrp1
Wfdc21
Mmp8
had
high
potential
targets
neutrophils.
highlights
interacting
cells,
corresponding
molecules,
underlying
treating
HBV‐associated
The
commensal
microbiota
provides
immunomodulatory
signals
during
the
development,
differentiation
and
activation
of
immune
cells,
is
crucial
for
maintaining
host
homeostasis.
However,
systematic
effects
on
immunity
based
large
animal
model
at
single-cell
level
remain
to
be
resolved.
Here,
we
utilized
RNA
sequencing
(scRNA-seq)
analyze
transcriptome
profiling
containing
57,720
cells
from
three
important
tissues
[Peyer's
patches
(PP),
mesenteric
lymph
node
(MLN),
spleen]
germ-free
(GF)
specific
pathogen-free
(SPF)
piglet.
We
presented
detailed
description
dataset
preliminarily
identified
major
cell
types
including
non-immune
further
annotated
subsets.
This
a
data
mining
resource
researchers
involved
in
microbe-host
interactions,
enables
in-depth
analysis
map
alterations
caused
by
colonization
early
development.
As
first
transcriptomics
tissue
GF
SPF
piglet,
this
valuable
study
regulation.
Background.
Machine
perfusion
is
the
preferred
preservation
method
for
deceased
donor
kidneys.
Perfusate
fluid,
which
contains
a
complex
mixture
of
components,
offers
potential
insight
into
organ’s
viability
and
function.
This
study
explored
immune
cell
release,
particularly
tissue-resident
lymphocytes
(TRLs),
during
kidney
machine
its
correlation
with
injury
markers.
Methods.
samples
from
hypothermic
(HMP;
n
=
26)
normothermic
(NMP;
16)
human
kidneys
were
analyzed
TRLs
using
flow
cytometry.
Residency
was
defined
by
expressions
CD69,
CD103,
CD49as.
TRL
release
quantified
exclusively
in
NMP.
Additionally,
levels
cell-free
DNA,
neutrophil
gelatinase-associated
lipocalin,
soluble
E-cadherin
(sE-cadherin)
measured
NMP
supernatants
quantitative
polymerase
chain
reaction
enzyme-linked
immunosorbent
assay.
Results.
Both
HMP
contained
heterogeneous
population
TRLs,
including
CD4
+
memory
T
cells,
CD8
natural
killer
helper-like
innate
lymphoid
cells.
Median
proportions
among
total
CD45
0.89%
(NMP)
0.84%
(HMP).
quantities
did
not
correlate
characteristics,
parameters,
posttransplant
outcomes,
or
DNA
lipocalin
concentrations.
However,
CD103
positively
correlated
sE-cadherin,
ligand
integrin.
Conclusions.
Human
both
The
associated
loss
their
sE-cadherin
but
general
transplant
biomarkers.