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Disease-specific induced pluripotent stem cells: a platform for human disease modeling and drug discovery.
[adrenomyeloneuropathy]
The
generation
of
disease-
specific
induced
pluripotent
stem
cell
(
iPSC
)
lines
from
patients
with
incurable
diseases
is
a
promising
approach
for
studying
disease
mechanisms
and
drug
screening
.
Such
innovation
enables
to
obtain
autologous
cell
sources
in
regenerative
medicine
.
Herein
,
we
report
the
generation
and
characterization
of
iPSCs
from
fibroblasts
of
patients
with
sporadic
or
familial
diseases
,
including
Parkinson
's
disease
(
PD
)
,
Alzheimer
's
disease
(
AD
)
,
juvenile
-onset
,
type
I
diabetes
mellitus
(
JDM
)
,
and
Duchenne
type
muscular
dystrophy
(
DMD
)
,
as
well
as
from
normal
human
fibroblasts
(
WT
)
.
As
an
example
to
modeling
disease
using
disease-
specific
iPSCs
,
we
also
discuss
the
previously
established
childhood
cerebral
adrenoleukodystrophy
(
CCALD
)
-
and
adrenomyeloneuropathy
(
AMN
)
-
iPSCs
by
our
group
.
Through
DNA
fingerprinting
analysis
,
the
origins
of
generated
disease-
specific
iPSC
lines
were
identified
.
Each
iPSC
line
exhibited
an
intense
alkaline
phosphatase
activity
,
expression
of
pluripotent
markers
,
and
the
potential
to
differentiate
into
all
three
embryonic
germ
layers
:
the
ectoderm
,
endoderm
,
and
mesoderm
.
Expression
of
endogenous
pluripotent
markers
and
downregulation
of
retrovirus-delivered
transgenes
[
OCT
4
(
POU
5
F
1
)
,
SOX
2
,
KLF
4
,
and
c-
MYC
]
were
observed
in
the
generated
iPSCs
.
Collectively
,
our
results
demonstrated
that
disease-
specific
iPSC
lines
characteristically
resembled
hESC
lines
.
Furthermore
,
we
were
able
to
differentiate
PD-iPSCs
,
one
of
the
disease-
specific
-i
PSC
lines
we
generated
,
into
dopaminergic
(
DA
)
neurons
,
the
cell
type
mostly
affected
by
PD
.
These
PD-
specific
DA
neurons
along
with
other
examples
of
cell
models
derived
from
disease-
specific
iPSCs
would
provide
a
powerful
platform
for
examining
the
pathophysiology
of
relevant
diseases
at
the
cellular
and
molecular
levels
and
for
developing
new
drugs
and
therapeutic
regimens
.
Diseases
Validation
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"we also discuss the previously established childhood cerebral adrenoleukodystrophy"
symptom
adrenomyeloneuropathy
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