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Sphingosine-1-phosphate receptors control B-cell migration through signaling components associated with primary immunodeficiencies, chronic lymphocytic leukemia, and multiple sclerosis.
[wiskott-aldrich syndrome]
Five
different
G
protein-coupled
sphingosine-
1
-
phosphate
(
S
1
P
)
receptors
(
S
1
P
1
-
S
1
P
5
)
regulate
a
variety
of
physiologic
and
pathophysiologic
processes
,
including
lymphocyte
circulation
,
multiple
sclerosis
(
MS
)
,
and
cancer
.
Although
B-
lymphocyte
circulation
plays
an
important
role
in
these
processes
and
is
essential
for
normal
immune
responses
,
little
is
known
about
S
1
P
receptors
in
human
B
cells
.
To
explore
their
function
and
signaling
,
we
studied
B-
cell
lines
and
primary
B
cells
from
control
subjects
,
patients
with
leukemia
,
patients
with
S
1
P
receptor
inhibitor-treated
MS
,
and
patients
with
primary
immunodeficiencies
.
S
1
P
receptor
expression
was
analyzed
by
using
multicolor
immunofluorescence
microscopy
and
quantitative
PCR
.
Transwell
assays
were
used
to
study
cell
migration
.
S
1
P
receptor
internalization
was
visualized
by
means
of
time-lapse
imaging
with
fluorescent
S
1
P
receptor
fusion
proteins
expressed
by
using
lentiviral
gene
transfer
.
B-
lymphocyte
subsets
were
characterized
by
means
of
flow
cytometry
and
immunofluorescence
microscopy
.
Showing
that
different
B-
cell
populations
express
different
combinations
of
S
1
P
receptors
,
we
found
that
S
1
P
1
promotes
migration
,
whereas
S
1
P
4
modulates
and
S
1
P
2
inhibits
S
1
P
1
signals
.
Expression
of
CD
69
in
activated
B
lymphocytes
and
B
cells
from
patients
with
chronic
lymphocytic
leukemia
inhibited
S
1
P
-
induced
migration
.
Studying
B-
cell
lines
,
normal
B
lymphocytes
,
and
B
cells
from
patients
with
primary
immunodeficiencies
,
we
identified
Bruton
tyrosine
kinase
,
β-arrestin
2
,
LPS-responsive
beige-like
anchor
protein
,
dedicator
of
cytokinesis
8
,
and
Wiskott-
Aldrich
syndrome
protein
as
critical
signaling
components
downstream
of
S
1
P
1
.
Thus
S
1
P
receptor
signaling
regulates
human
B-
cell
circulation
and
might
be
a
factor
contributing
to
the
pathology
of
MS
,
chronic
lymphocytic
leukemia
,
and
primary
Â
immunodeficiencies
.
Diseases
Validation
Diseases presenting
"cancer"
symptom
achondroplasia
acute rheumatic fever
adrenal incidentaloma
alpha-thalassemia
benign recurrent intrahepatic cholestasis
cadasil
canavan disease
carcinoma of the gallbladder
cholangiocarcinoma
coats disease
congenital adrenal hyperplasia
congenital diaphragmatic hernia
cowden syndrome
cushing syndrome
cutaneous mastocytosis
dedifferentiated liposarcoma
dystrophic epidermolysis bullosa
epidermolysis bullosa simplex
erdheim-chester disease
erythropoietic protoporphyria
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
familial hypocalciuric hypercalcemia
familial mediterranean fever
gm1 gangliosidosis
heparin-induced thrombocytopenia
hereditary cerebral hemorrhage with amyloidosis
hirschsprung disease
hodgkin lymphoma, classical
inclusion body myositis
junctional epidermolysis bullosa
kabuki syndrome
kallmann syndrome
kindler syndrome
lamellar ichthyosis
liposarcoma
locked-in syndrome
lymphangioleiomyomatosis
monosomy 21
neuralgic amyotrophy
oculocutaneous albinism
oligodontia
oral submucous fibrosis
papillon-lefèvre syndrome
pendred syndrome
pleomorphic liposarcoma
primary effusion lymphoma
proteus syndrome
pyomyositis
pyruvate dehydrogenase deficiency
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
von hippel-lindau disease
waldenström macroglobulinemia
well-differentiated liposarcoma
werner syndrome
wiskott-aldrich syndrome
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
This symptom has already been validated