The 40S ribosomal subunit recycling complex modulates mitochondrial dynamics and endoplasmic reticulum - mitochondria tethering at mitochondrial fission/fusion hotspots
Foozhan Tahmasebinia,
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Yinglu Tang,
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Rushi Tang
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et al.
Nature Communications,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Jan. 25, 2025
The
40S
ribosomal
subunit
recycling
pathway
is
an
integral
link
in
the
cellular
quality
control
network,
occurring
after
translational
errors
have
been
corrected
by
ribosome-associated
(RQC)
machinery.
Despite
our
understanding
of
its
role,
impact
translation
on
metabolism
remains
poorly
understood.
Here,
we
reveal
a
conserved
role
(USP10-G3BP1)
complex
regulating
mitochondrial
dynamics
and
function.
binds
to
fission-fusion
proteins
located
at
hotspots,
functional
assembly
endoplasmic
reticulum-mitochondria
contact
sites
(ERMCSs).
Furthermore,
it
alters
activity
mTORC1/2
pathways,
suggesting
between
energy
fluctuations.
Effective
communication
essential
for
resolving
proteostasis-related
stresses.
Our
study
illustrates
that
USP10-G3BP1
acts
as
hub
interacts
with
various
pathways
adapt
environmental
stimuli
promptly.
It
advances
molecular
RQC
regulation
helps
explain
pathogenesis
human
proteostasis
dysfunction
diseases.
Coordinating
protein
supply
significant
challenge
faced
cells.
authors
found
network
may
provide
two.
Language: Английский
Investigating cognitive impairments and hippocampal proteome alterations in aged male rats with TAA-Induced minimal hepatic encephalopathy
Biogerontology,
Journal Year:
2024,
Volume and Issue:
26(1)
Published: Dec. 20, 2024
Language: Английский
Investigating Hippocampal Proteome Dynamics in Aging Rats with Minimal Hepatic Encephalopathy via High-Resolution Mass Spectrometry
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 1, 2024
Abstract
The
aging
population
faces
a
gradual
decline
in
physical
and
mental
capacities,
with
an
increased
risk
of
liver
cirrhosis
chronic
diseases
leading
to
hepatic
encephalopathy
(HE).
intertwining
physiological
manifestations
the
pathophysiology
HE
significantly
impairs
cognitive
ability,
reduces
quality
life,
increases
mortality.
Hence,
effective
therapeutic
intervention
is
imperative.
present
study
investigated
impact
minimal
(MHE)
on
impairment
rat
by
analyzing
hippocampal
proteome
dynamics.
For
this
purpose,
old
MHE
model
was
induced
via
thioacetamide.
label-free
LC‒MS/MS
method
employed
explore
proteomic
changes
associated
dysregulated
biological
pathways.
A
total
1533
proteins
were
identified,
among
these,
30
differentially
expressed
(18
upregulated,
12
downregulated).
Three
upregulated
proteins,
namely,
fetuin-A,
p23,
intersectin-1
selected
validated
for
their
expression
western
blotting
immunofluorescence
analysis,
which
confirmed
mass
spectrometry
results.
These
have
not
been
reported
previously
cases.
We
also
identified
possible
pathways
Metascape,
network
analysis
tool.
found
that
may
be
involved
generation
precursor
metabolites
energy,
neurotransmitter
release
cycle,
positive
regulation
dendritic
spine
development,
chaperone-mediated
protein
folding
stabilization.
This
highlights
potential
mechanisms
underlying
neurological
dysfunction
identifies
novel
targets
improved
disease
management.
Language: Английский