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Evidence for decreased lipofibroblast expression in hypoplastic rat lungs with congenital diaphragmatic hernia.
[congenital diaphragmatic hernia]
Pulmonary
hypoplasia
(
PH
)
is
a
serious
condition
in
newborns
with
congenital
diaphragmatic
hernia
(
CDH
)
.
Lipid-containing
interstitial
fibroblasts
(
LIFs
)
play
an
essential
role
in
fetal
lung
maturation
by
stimulating
alveolarization
and
lipid
homeostasis
.
In
rodents
,
LIFs
are
first
evident
during
the
canalicular
phase
of
lung
development
with
a
significant
increase
over
the
last
4
Â
days
of
gestation
.
Adipocyte
differentiation-related
protein
(
ADRP
)
,
a
functional
lipogenic
molecular
marker
characterizing
LIFs
,
is
highly
expressed
in
fetal
lungs
during
this
critical
time
period
.
We
hypothesized
that
LIF
expression
in
hypoplastic
rat
lungs
is
decreased
in
the
nitrofen-induced
CDH
model
,
which
is
accompanied
by
reduced
alveolar
ADRP
expression
and
lipid
content
.
On
embryonic
day
9
.
5
(
E
9
.
5
)
,
time-mated
rats
received
either
nitrofen
or
vehicle
.
Fetuses
were
sacrificed
on
selected
time
points
E
18
.
5
and
E
21
.
5
,
and
dissected
lungs
were
divided
into
controls
and
CDH
-associated
PH
.
Pulmonary
gene
expression
levels
of
ADRP
were
determined
by
quantitative
real-time
polymerase
chain
reaction
.
ADRP
immunohistochemistry
and
oil
red
O
staining
were
used
to
assess
pulmonary
protein
expression
and
lipid
content
.
Immunofluorescence
double
staining
for
alpha
smooth
muscle
actin
,
which
is
known
to
be
absent
in
LIFs
,
and
lipid
droplets
was
performed
to
evaluate
the
pulmonary
expression
of
this
specific
subset
of
fibroblasts
.
Relative
mRNA
expression
of
ADRP
was
significantly
reduced
in
lungs
of
CDH
-associated
PH
on
E
18
.
5
and
E
21
.
5
compared
to
controls
.
ADRP
immunoreactivity
and
lipid
staining
were
markedly
diminished
in
alveolar
mesenchymal
cells
of
CDH
-associated
PH
on
E
18
.
5
and
E
21
.
5
compared
to
controls
.
Confocal
laser
scanning
microscopy
demonstrated
markedly
decreased
LIF
expression
in
alveolar
interstitium
of
CDH
-associated
PH
on
E
18
.
5
and
E
21
.
5
compared
to
controls
.
Decreased
pulmonary
LIF
expression
during
late
gestation
suggests
impaired
LIF
functioning
in
the
nitrofen-induced
CDH
model
,
which
may
cause
disruption
in
fetal
alveolarization
and
lipid
homeostasis
,
and
thus
contribute
to
the
development
of
PH
.
Diseases
Validation
Diseases presenting
"which is known to be absent in lifs"
symptom
congenital diaphragmatic hernia
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