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Authordc.contributor.authorCastro, Isabel 
Authordc.contributor.authorAguilera, Sergio es_CL
Authordc.contributor.authorBrockhausen, Inka es_CL
Authordc.contributor.authorAlliende, Cecilia es_CL
Authordc.contributor.authorQuest, Andrew F. G. es_CL
Authordc.contributor.authorMolina, Claudio es_CL
Authordc.contributor.authorUrzúa Tobar, Ulises es_CL
Authordc.contributor.authorMandel, Ulla es_CL
Authordc.contributor.authorBahamondes, Verónica es_CL
Authordc.contributor.authorBarrera, María José es_CL
Authordc.contributor.authorSánchez, Marianela es_CL
Authordc.contributor.authorGonzález, Sergio es_CL
Authordc.contributor.authorHermoso Ramello, Marcela es_CL
Authordc.contributor.authorLeyton Martínez, Cecilia es_CL
Authordc.contributor.authorGonzález Burgos, María Julieta es_CL
Admission datedc.date.accessioned2012-05-28T20:36:38Z
Available datedc.date.available2012-05-28T20:36:38Z
Publication datedc.date.issued2012
Cita de ítemdc.identifier.citationRheumatology 2012;51:482-490es_CL
Identifierdc.identifier.otherdoi:10.1093/rheumatology/ker351
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/128962
Abstractdc.description.abstractObjectives. To determine the expression and enzymatic activities of sulphotransferases involved in mucin hyposulphation in labial salivary glands (LSGs) from SS patients and to correlate sulphotransferase activity with clinical parameters such as secretion, inflammation and serology. Methods. LSG from 31 SS patients and 31 control subjects were studied. Relative mRNA and protein levels of Gal3-O-sulphotransferases (Gal3STs) and b1,3-galactosyltransferase-5 (b3GalT5) were determined by quantitative RT-PCR and western blotting, respectively. Enzymatic activities were quantified using radioactively labelled donor substrates and specific acceptor substrates. Products were purified by chromatography. Spearman’s correlation analysis was used to compare data. Results. The levels of Gal3ST activity were significantly decreased in SS patients, without changes in mRNA and protein levels, while the enzymatic activities of glycosyltransferases involved in mucin glycosylation were similar in both groups. An inverse correlation was observed between Gal3ST activity and glandular function measured by scintigraphy, but not with unstimulated salivary flow. Gal3ST activity was inversely correlated with focus score, TNF-a levels and presence of the autoantibodies Ro/SS-A and La/SS-B. Conclusion. The decrease in sulphotransferase activity provides an explanation for mucin hyposulphation observed in the LSGs from SS patients. The decrease in Gal3STs activity was not a consequence of reduced gene expression, but probably due to alterations in the enzyme activity regulation. Interestingly, the levels of sulphotransferase activity detected correlated well with secretory function, inflammation and serology. Finally, we postulate that pro-inflammatory cytokines induced by autoantibodies, such as Ro/SS-A and La/SS-B in SS patients, may modulate Gal3ST activity, thereby altering mucin quality and leading to mouth dryness.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherOxford University Presses_CL
Keywordsdc.subjectSjögren’s syndromees_CL
Títulodc.titleDecreased salivary sulphotransferase activity correlated with inflammation and autoimmunity parameters in Sjögren’s syndrome patientses_CL
Document typedc.typeArtículo de revista


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