MUC1/SEC and MUC1/Y overexpression is associated with inflammation in Sjogren's syndrome
Author
dc.contributor.author
Sung Hsieh, Hsiao
Author
dc.contributor.author
Castro, I.
Author
dc.contributor.author
González, S.
Author
dc.contributor.author
Aguilera, S.
Author
dc.contributor.author
Smorodinsky, N. I.
Author
dc.contributor.author
Quest, Andrew F. G.
Author
dc.contributor.author
Bahamondes Lorca, Verónica
Author
dc.contributor.author
Alliende, Cecilia
Author
dc.contributor.author
Cortés, J.
Author
dc.contributor.author
Molina, Claudio
Author
dc.contributor.author
Urzúa Tobar, Ulises
Author
dc.contributor.author
Barrera, María José
Author
dc.contributor.author
Hermoso Ramello, Marcela
Author
dc.contributor.author
Herrera Cisterna, Luisa
Author
dc.contributor.author
Leyton Martínez, Cecilia
Author
dc.contributor.author
González Burgos, María Julieta
Admission date
dc.date.accessioned
2015-10-29T20:12:33Z
Available date
dc.date.available
2015-10-29T20:12:33Z
Publication date
dc.date.issued
2015
Cita de ítem
dc.identifier.citation
Oral Diseases (2015) 21, 730–738
en_US
Identifier
dc.identifier.other
doi:10.1111/odi.12339
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/134769
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
OBJECTIVES: To evaluate the expression and localization
of MUC1/SEC and MUC1/Y isoforms in labial salivary
glands (LSG) from Sj€ogren’s syndrome patients
(SS patients), as well as their in vitro expression induced
by cytokines.
SUBJECTS AND METHODS: Labial salivary gland from
27 primary SS patients and 22 non-SS sicca subjects
were studied. Relative MUC1/SEC and MUC1/Y mRNA
levels were determined by qPCR and protein levels by
Western blotting. Induction of mucin mRNAs was
assayed in vitro. Immunohistochemistry was used for
localization.
RESULTS: Relative MUC1/SEC and MUC1/Y mRNA and
protein levels were significantly higher in LSG from SS
patients. These mRNAs were induced by cytokines.
MUC1/SEC and MUC1/Y were detected in acini apical
region of control LSGs, and significant cytoplasmic
accumulation was observed in acini of SS patients.
MUC1/Y localized in acinar nuclei and cytoplasm of
inflammatory cells of LSG from SS patients. A strong
positive correlation was observed between cellular
MUC1/SEC levels and glandular function determined by
scintigraphy.
CONCLUSIONS: We show for the first time that
MUC1/SEC and MUC1/Y are expressed in LSG of both
SS patients and non-SS sicca subjects. The observed
overexpression and aberrant localization of MUC1/SEC
and MUC1/Y and their induction by pro-inflammatory
cytokines may favor the perpetuation of the inflammatory
environment that disrupts the salivary glandular
homeostasis in SS patients.