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Reduced expression of dentin sialophosphoprotein is associated with dysplastic dentin in mice overexpressing transforming growth factor-beta 1 in teeth.
[dentin dysplasia]
Transforming
growth
factor
(
TGF
)
-
beta
1
is
expressed
in
developing
tooth
from
the
initiation
stage
through
adulthood
.
Odontoblast-
specific
expression
of
TGF-
beta
1
in
the
tooth
continues
throughout
life
;
however
,
the
precise
biological
functions
of
this
growth
factor
in
the
odontoblasts
are
not
clearly
understood
.
Herein
,
we
describe
the
generation
of
transgenic
mice
that
overexpress
active
TGF-
beta
1
predominantly
in
the
odontoblasts
.
Teeth
of
these
mice
show
a
significant
reduction
in
the
tooth
mineralization
,
defective
dentin
formation
,
and
a
relatively
high
branching
of
dentinal
tubules
.
Dentin
extracellular
matrix
components
such
as
type
I
and
III
collagens
are
increased
and
deposited
abnormally
in
the
dental
pulp
,
similar
to
the
hereditary
human
tooth
disorders
such
as
dentin
dysplasia
and
dentinogenesis
imperfecta
.
Calcium
,
one
of
the
crucial
inorganic
components
of
mineralization
,
is
also
apparently
increased
in
the
transgenic
mouse
teeth
.
Most
importantly
,
the
expression
of
dentin
sialophosphoprotein
(
dspp
)
,
a
candidate
gene
implicated
in
dentinogenesis
imperfecta
II
(
MIM
125420
)
,
is
significantly
down-regulated
in
the
transgenic
teeth
.
Our
results
provide
in
vivo
evidence
suggesting
that
TGF-
beta
1
mediated
expression
of
dspp
is
crucial
for
dentin
mineralization
.
These
findings
also
provide
for
the
first
time
a
direct
experimental
evidence
indicating
that
decreased
dspp
gene
expression
along
with
the
other
cellular
changes
in
odontoblasts
may
result
in
human
hereditary
dental
disorders
like
dentinogenesis
imperfecta
II
(
MIM
125420
)
and
dentin
dysplasia
(
MIM
125400
and
125420
)
.
Diseases
Validation
Diseases presenting
"first time"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
adrenomyeloneuropathy
alpha-thalassemia
aniridia
aromatase deficiency
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
classical phenylketonuria
congenital adrenal hyperplasia
congenital toxoplasmosis
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dentin dysplasia
dentinogenesis imperfecta
dracunculiasis
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial mediterranean fever
gm1 gangliosidosis
harlequin ichthyosis
heparin-induced thrombocytopenia
hirschsprung disease
hodgkin lymphoma, classical
holt-oram syndrome
hydrocephalus with stenosis of the aqueduct of sylvius
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
malignant atrophic papulosis
megacystis-microcolon-intestinal hypoperistalsis syndrome
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
omenn syndrome
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
phenylketonuria
primary effusion lymphoma
primary hyperoxaluria type 1
severe combined immunodeficiency
sneddon syndrome
triple a syndrome
trochlear dysplasia
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
zellweger syndrome
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