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Oxidative stress modulates mitochondrial failure and cyclophilin D function in X-linked adrenoleukodystrophy.
[x-linked adrenoleukodystrophy]
A
common
process
associated
with
oxidative
stress
and
severe
mitochondrial
impairment
is
the
opening
of
the
mitochondrial
permeability
transition
pore
,
as
described
in
many
neurodegenerative
diseases
.
Thus
,
inhibition
of
mitochondrial
permeability
transition
pore
opening
represents
a
potential
target
for
inhibiting
mitochondrial
-driven
cell
death
.
Among
the
mitochondrial
permeability
transition
pore
components
,
cyclophilin
D
is
the
most
studied
and
has
been
found
increased
under
pathological
conditions
.
Here
,
we
have
used
in
vitro
and
in
vivo
models
of
X-
linked
adrenoleukodystrophy
to
investigate
the
relationship
between
the
mitochondrial
permeability
transition
pore
opening
and
redox
homeostasis
.
X-
linked
adrenoleukodystrophy
is
a
neurodegenerative
condition
caused
by
loss
of
function
of
the
peroxisomal
ABCD
1
transporter
,
in
which
oxidative
stress
plays
a
pivotal
role
.
In
this
study
,
we
provide
evidence
of
impaired
mitochondrial
metabolism
in
a
peroxisomal
disease
,
as
fibroblasts
in
patients
with
X-
linked
adrenoleukodystrophy
can
not
survive
when
forced
to
rely
on
mitochondrial
energy
production
,
i
.
e
.
on
incubation
in
galactose
.
Oxidative
stress
induced
under
galactose
conditions
leads
to
mitochondrial
damage
in
the
form
of
mitochondrial
inner
membrane
potential
dissipation
,
ATP
drop
and
necrotic
cell
death
,
together
with
increased
levels
of
oxidative
modifications
in
cyclophilin
D
protein
.
Moreover
,
we
show
increased
expression
levels
of
cyclophilin
D
in
the
affected
zones
of
brains
in
patients
with
adrenomyeloneuropathy
,
in
spinal
cord
of
a
mouse
model
of
X-
linked
adrenoleukodystrophy
(
Abcd
1
-
null
mice
)
and
in
fibroblasts
from
patients
with
X-
linked
adrenoleukodystrophy
.
Notably
,
treatment
with
antioxidants
rescues
mitochondrial
damage
markers
in
fibroblasts
from
patients
with
X-
linked
adrenoleukodystrophy
,
including
cyclophilin
D
oxidative
modifications
,
and
reverses
cyclophilin
D
induction
in
vitro
and
in
vivo
.
These
findings
provide
mechanistic
insight
into
the
beneficial
effects
of
antioxidants
in
neurodegenerative
and
non-neurodegenerative
cyclophilin
D-
dependent
disorders
.
Diseases
Validation
Diseases presenting
"mitochondrial permeability transition pore opening"
symptom
adrenomyeloneuropathy
x-linked adrenoleukodystrophy
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