ROS Induced by Aphrocallistes vastus Lectin Enhance Oncolytic Vaccinia Virus Replication and Induce Apoptosis in Hepatocellular Carcinoma Cells
Yanan Zhang,
No information about this author
Ying Zhu,
No information about this author
Gaohui Jiang
No information about this author
et al.
Marine Drugs,
Journal Year:
2024,
Volume and Issue:
22(7), P. 307 - 307
Published: June 30, 2024
Oncolytic
virotherapy
is
expected
to
provide
a
new
treatment
strategy
for
cancer.
Aphrocallistes
vastus
lectin
(AVL)
Ca2+-dependent
receptor
containing
the
conserved
domain
of
C-type
and
hydrophobic
N-terminal
region,
which
can
bind
bird’s
nest
glycoprotein
D-galactose.
Our
previous
studies
suggested
that
oncolytic
vaccinia
virus
(oncoVV)
armed
with
AVL
gene
exerted
remarkable
replication
antitumor
effects
in
vitro
vivo.
In
this
study,
we
found
oncoVV-AVL
may
reprogram
metabolism
hepatocellular
carcinoma
cells
promote
ROS,
elevated
ROS
subsequently
promoted
viral
induced
apoptosis.
This
study
will
theoretical
basis
application
liver
Language: Английский
Mitochondria-dependent innate immunity: A potential therapeutic target in Flavivirus infection
International Immunopharmacology,
Journal Year:
2025,
Volume and Issue:
154, P. 114551 - 114551
Published: March 31, 2025
Language: Английский
A mitochondrion-targeted poly(N-isopropylacrylamide-coacrylic acid) nanohydrogel with a fluorescent bioprobe for ferrous ion imaging in vitro and in vivo
Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy,
Journal Year:
2025,
Volume and Issue:
330, P. 125725 - 125725
Published: Jan. 9, 2025
Language: Английский
scRNA seq of an F1 cross of Marek’s disease resistant and susceptible chickens identifies allele specific expression signatures enriched in transcription modulators
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 29, 2025
Language: Английский
Enterovirus A71-induced glycolysis is essential for viral replication by activating PI3K/Akt pathway
Li Dan,
No information about this author
Jing Yang,
No information about this author
Yijun Shen
No information about this author
et al.
Microbial Pathogenesis,
Journal Year:
2025,
Volume and Issue:
unknown, P. 107505 - 107505
Published: March 1, 2025
Language: Английский
Mitochondrial resilience and antioxidant defence against HIV-1: unveiling the power of Asparagus racemosus extracts and Shatavarin IV
Frontiers in Microbiology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 23, 2024
Asparagus
racemosus
(AR),
an
Ayurvedic
botanical,
possesses
various
biological
characteristics,
yet
its
impact
on
HIV-1
replication
remains
to
be
elucidated.
This
study
aimed
investigate
the
inhibitory
effects
of
AR
root
extracts
and
principal
bioactive
molecule,
Shatavarin
IV
(Shatavarin),
their
role
in
mitigating
mitochondrial
dysfunction
during
infection,
utilizing
both
vitro
silico
methodologies.
The
cytotoxicity
was
evaluated
using
MTT
ATPlite
assays.
In
anti-HIV-1
activity
assessed
TZM-bl
cells
against
X4
R5
subtypes,
confirmed
peripheral
blood
mononuclear
p24
antigen
capture
ELISA
viral
copy
number
assessment.
Mechanistic
insights
were
obtained
through
enzymatic
assays
targeting
Integrase,
Protease
Reverse
Transcriptase.
Shatavarin’s
also
validated
via
assays,
along
with
molecular
interaction
studies
key
enzymes.
induced
by
detecting
reactive
oxygen
species
(ROS),
calcium
accumulation,
potential,
caspase
within
infected
cells.
Non-cytotoxic
concentrations
aqueous
hydroalcoholic
derived
from
roots
displayed
dose-dependent
inhibition
replication.
Notably,
extract
exhibited
superior
Transcriptase
activity,
complemented
moderate
observed
assay.
Molecular
revealed
that
IV,
constituent
AR,
formed
hydrogen
bonds
active
binding
pocket
site
residues
crucial
for
HIV
enzyme
catalysis,
suggesting
potential
attenuating
infection.
Mitochondrial
marked
increased
oxidative
stress,
overload,
loss
membrane
elevated
effectively
mitigated
treatment
IV.
These
findings
underscore
as
antiviral
agents,
while
enhancing
function
conclusion,
extracts,
particularly
demonstrate
promising
concurrently
ameliorating
virus.
suggest
therapeutic
combating
infection
improving
health.
Language: Английский
Physiological Adaptation of Fenneropenaeus chinensis in Response to Saline–Alkaline Stress Revealed by a Combined Proteomics and Metabolomics Method
Tian Gao,
No information about this author
Qiong Wang,
No information about this author
Huarui Sun
No information about this author
et al.
Biology,
Journal Year:
2024,
Volume and Issue:
13(7), P. 488 - 488
Published: June 30, 2024
The
rapid
development
of
the
mariculture
industry
has
been
hindered
by
limited
coastal
aquaculture
space.
To
utilize
abundant
inland
saline-alkaline
water,
we
studied
physiological
effects
high
carbonate
alkalinity
stress
and
pH
on
Language: Английский
Immunometabolites in viral infections: Action mechanism and function
Behnaz Bouzari,
No information about this author
Uliana Y. Chugaeva,
No information about this author
Sajad Karampoor
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et al.
Journal of Medical Virology,
Journal Year:
2024,
Volume and Issue:
96(7)
Published: July 1, 2024
Abstract
The
interplay
between
viral
pathogens
and
host
metabolism
plays
a
pivotal
role
in
determining
the
outcome
of
infections.
Upon
detection,
metabolic
landscape
cell
undergoes
significant
changes,
shifting
from
oxidative
respiration
via
tricarboxylic
acid
(TCA)
cycle
to
increased
aerobic
glycolysis.
This
shift
is
accompanied
by
elevated
nutrient
accessibility,
which
vital
for
function,
development,
proliferation.
Furthermore,
depositing
metabolites
derived
fatty
acids,
TCA
intermediates,
amino
catabolism
accelerates
immunometabolic
transition,
facilitating
pro‐inflammatory
antimicrobial
responses.
Immunometabolites
refer
small
molecules
involved
cellular
regulating
immune
response.
These
include
nutrients,
such
as
glucose
along
with
intermediates
signaling
adenosine,
lactate,
itaconate,
succinate,
kynurenine,
prostaglandins.
Emerging
evidence
suggests
that
immunometabolites
released
cells
establish
complex
interaction
network
within
local
niches,
orchestrating
fine‐tuning
responses
during
diseases.
However,
our
current
understanding
immense
capacity
convey
essential
signals
one
another
or
compartments
remains
incomplete.
Unraveling
these
complexities
would
be
crucial
harnessing
potential
therapeutic
interventions.
In
this
review,
we
discuss
specific
their
mechanisms
action
infections,
emphasizing
recent
findings
future
directions
rapidly
evolving
field.
Language: Английский
Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus
Gaoyan G. Tang‐Siegel,
No information about this author
David W. Maughan,
No information about this author
Milah B. Frownfelter
No information about this author
et al.
Case Reports in Genetics,
Journal Year:
2024,
Volume and Issue:
2024, P. 1 - 10
Published: May 9, 2024
Myalgic
encephalomyelitis/chronic
fatigue
syndrome
(ME/CFS)
is
a
multisystem
disabling
disease
with
unclear
etiology
and
pathophysiology,
whose
typical
symptoms
include
prolonged
debilitating
recovery
from
or
postexertional
malaise
(PEM).
Disrupted
production
of
adenosine
triphosphate
(ATP),
the
intracellular
energy
that
fuels
cellular
activity,
cause
for
fatigue.
Here,
we
present
long-term
case
ME/CFS:
75-year-old
Caucasian
female
patient,
ME/CFS
were
clearly
triggered
by
an
acute
infection
Epstein–Barr
virus
24
years
ago
(mononucleosis).
Before
then,
patient
was
healthy
professional
woman.
A
recent
DNA
sequence
analysis
identified
missense
variants
mitochondrial
respiratory
chain
enzymes,
including
ATP6
(ChrMT:
8981A
>
G;
Q152R)
Cox1
6268C
T;
A122V).
Protein
subunits
are
encoded
outside
nucleus:
gene
encodes
subunit
1
complex
IV
(CIV:
cytochrome
c
oxidase)
V
(CV:
ATP
synthase).
CIV
CV
last
two
five
essential
enzymes
perform
electron
transport
reaction
to
generate
ATP.
Further
blood
sample
using
transmission
microscopy
demonstrated
abnormal,
circulating,
extracellular
mitochondria.
These
results
indicate
had
dysfunctional
mitochondria,
which
may
contribute
directly
her
major
symptoms,
PEM
neurological
cognitive
changes.
Furthermore,
A122V),
functioning
at
later
stage
production,
play
role
in
abnormality
patient’s
mitochondria
development
symptoms.
Language: Английский
Mitochondrial morphodynamics are modulated by physiological range of temperature and influence host cell outcomes during influenza infection
Grant J. McLoughlin,
No information about this author
Andrew Pekosz
No information about this author
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 6, 2024
Abstract
Influenza
viruses
replicate
in
both
the
cooler,
upper
portions
of
airway
and
warmer,
lower
respiratory
tract.
This
study
investigates
how
physiological
ranges
temperature,
specifically
33°C
37°C,
impact
host
cell
biology
temperature-dependent
differences
cells
influence
outcomes
during
influenza
A
virus
infection.
prioritizes
describing
mitochondrial
networks
due
to
their
importance
maintaining
cellular
homeostasis
mediating
immune
responses
viral
The
temperature
at
which
are
incubated
significantly
influences
network
morphology
function.
Moreover,
changes
prior
infection
result
temperature-specific
These
findings
indicate
that
structure
alone
can
modulate
form
function
mitochondria
directly
production.
While
not
all
processes
were
shown
be
affected
by
or
infection,
these
results
highlight
using
physiologically
relevant
temperatures
pathogen
research
elucidate
dynamics
contribute
Importance
Respiratory
infect
tract
but
rarely
is
(33°C
37°C)
considered.
Mitochondria
central
mediators
numerous
pathways,
functions
often
modified
Physiological
alter
function,
further
impacted
sheds
light
on
concert
with
Language: Английский