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Prolactin
Up-Regulates Cathepsin B and D Expression in Minor Salivary Glands of Patients
with Sjögren's Syndrome
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Serge Steinfeld,
Arielle Maho, Carole Chaboteaux, Philippe Daelemans, Roland Pochet, Thierry
Appelboom, and Robert Kiss
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Divisions
of Rheumatology (SS, TA) and Stomatology (PD), Erasme University Hospital,
IRIBHN<zaq;1> (AM), Laboratory of Histopathology (CC, RP, RK), Faculty
of Medicine, Universit|fe Libre de Bruxelles, Brussels, Belgium
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Various proteases are expressed in the minor salivary glands (MSG) of
patients with Sjögren's syndrome (SS), and as we have already shown,
prolactin is neosynthesized in the acinar cells of patients with SS. The
present study aims to characterize the influence of PRL on the expression
of cathepsin B and D in the MSG of patients with SS. Cathepsin B and D
expression was investigated immunohistochemically in MSG of 30 patients
with SS and 15 healthy volunteers. The presence of cathepsin B and D mRNAs
was checked in three SS patients and three control subjects by means of
reverse transcription-polymerase chain reaction (RT-PCR). The specificity
of the anti-cathepsin B and D antibodies used for the immunohistochemistry
was checked by means of western blotting analysis. The influence of prolactin
on the immunohistochemical expression of cathepsin B and D was quantitatively
assayed by computer-assisted microscopy at three different doses (5, 50,
and 500 ng/ml) on eight MSGs (four control subjects and four patients
with SS) maintained ex vivo under organotypic cultures. This influence
was also investigated at the mRNA level. Whereas cathepsin B immunopositivity
was absent from glandular epithelial cells of healthy subjects and only
slightly present in SS patients, cathepsin D immunoreactivity was considerably
greater (p < 0.0001) in both the acini and the ducts of patients
with SS as compared with control subjects. Cathepsin B, but not D, was
also expressed in about 20% of infiltrating mononuclear cells of SS patients.
Treatment of both healthy and SS minor salivary glands with PRL significantly
(p < 0.05 to p < 0.0001) enhanced cathepsin B and
D expression in acinar and ductal cells at both protein and mRNA levels.
PRL produced locally in MSGs of SS patients, but not those of healthy
subjects, could play a role in the pathogenesis of Sjögren's syndrome,
if only through the activation of proteolytic activity on the part of
cathepsins B and D.
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