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Sgk1 sensitive pendrin expression in murine platelets.
[pendred syndrome]
The
anion
exchanger
pendrin
(
SLC
26
A
4
)
is
required
for
proper
development
of
the
inner
ear
,
and
contributes
to
iodide
organification
in
thyroid
glands
as
well
as
anion
transport
in
various
epithelia
,
such
as
airways
and
renal
tubules
.
SLC
26
A
4
deficiency
leads
to
Pendred
syndrome
,
which
is
characterized
by
hearing
loss
with
enlarged
vestibular
aqueducts
and
variable
hypothyroidism
and
goiter
.
Pendrin
expression
in
kidney
,
heart
,
lung
and
thyroid
is
up-regulated
by
the
mineralocorticoid
deoxycorticosterone
(
DOCA
)
.
Platelets
express
anion
exchangers
but
virtually
nothing
is
known
about
the
molecular
identity
and
regulation
of
those
carriers
.
Other
carriers
such
as
the
Na
(
+
)
/
H
(
+
)
exchanger
are
regulated
by
the
mineralocorticoid-sensitive
serum
and
glucocorticoid
inducible
kinase
SGK
1
.
T
he
present
study
utilized
i
)
quantitative
reverse
transcription
polymerase
chain
reaction
(
RT-qPCR
)
to
quantify
the
transcript
levels
of
Slc
26
a
4
as
compared
to
Gapdh
and
ii
)
western
blotting
to
assess
Slc
26
a
4
protein
abundance
in
murine
platelets
from
gene
-targeted
mice
lacking
Sgk
1
(
sgk
1
(
-
/
-
)
)
and
respective
wild
type
animals
(
sgk
1
(
+
/
+
)
)
treated
without
or
with
a
subcutaneous
injection
of
2
.
5
mg
DOCA
for
3
h
,
or
in
sgk
1
(
+
/
+
)
platelets
with
or
without
in
vitro
treatment
for
1
h
with
10
µg
/
ml
DOCA
.
Slc
26
a
4
was
expressed
in
platelets
,
and
in
vitro
DOCA
treatment
increased
Slc
26
a
4
mRNA
levels
in
platelets
isolated
from
sgk
1
(
+
/
+
)
mice
.
Moreover
,
in
vivo
DOCA
treatment
significantly
up-regulated
Slc
26
a
4
mRNA
levels
in
platelets
isolated
from
sgk
1
(
+
/
+
)
but
not
sgk
1
(
-
/
-
)
mice
.
An
increase
in
Sgk
1
mRNA
levels
paralleled
that
of
Slc
26
a
4
mRNA
levels
in
platelets
of
sgk
1
(
+
/
+
)
mice
.
In
addition
,
DOCA
treatment
further
increased
Slc
26
a
4
protein
abundance
in
platelets
isolated
from
sgk
1
(
+
/
+
)
mice
.
Pendrin
is
expressed
in
platelets
and
is
presumably
regulated
by
SGK
1
and
mineralocorticoids
.
Diseases
Validation
Diseases presenting
"subcutaneous injection"
symptom
allergic bronchopulmonary aspergillosis
cutaneous mastocytosis
erythropoietic protoporphyria
esophageal carcinoma
esophageal squamous cell carcinoma
pendred syndrome
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