<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">1998</item><item key="factors"><item><item key="GSM1389620 1"/></item><item><item key="GSM1389619 1"/></item><item><item key="GSM1389618 1"/></item><item><item key="GSM1389617 1"/></item><item><item key="GSM1389616 1"/></item><item><item key="GSM1389615 1"/></item><item><item key="GSM1389614 1"/></item><item><item key="GSM1389613 1"/></item><item><item key="GSM1389612 1"/></item><item><item key="GSM1389611 1"/></item><item><item key="GSM1389610 1"/></item><item><item key="GSM1389609 1"/></item><item><item key="GSM1389608 1"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">&lt;Objective&gt; To compare gene expression in labial salivary glands (LSG) of IgG4-related disease (IgG4-RD) with Sj&#246;gren&#8217;s syndrome (SS)....</item><item key="pubmed_id">24943710</item><item key="geo_gse_id">E-GEOD-40568</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">13</item><item key="tags"><item>cell</item><item>chemokine</item><item>disease</item><item>keratoconjunctivitis</item><item>keratoconjunctivitis sicca</item><item>lymphocyte</item><item>organ</item><item>serum</item><item>syndrome</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-40568_A-AFFY-44</item><item key="slug">dna-microarray-analysis-of-labial-salivary-glands</item><item key="geo_gds_id"/><item key="name">DNA microarray analysis of labial salivary glands in IgG4-related disease &#8211; comparison with Sj&#246;gren&#8217;s syndrome</item><item key="created">Jul.10, 2014</item><item key="summary">&lt;Objective&gt; To compare gene expression in labial salivary glands (LSG) of IgG4-related disease (IgG4-RD) with Sj&#246;gren&#8217;s syndrome (SS). &lt;Methods&gt; Gene expression was analyzed by DNA microarray in LSG of IgG4-RD (n=5), SS (n=5), and healthy controls (n=3). Differentially expressed genes (DEGs) in IgG4-RD and SS were identified, and gene-annotation enrichment analysis of these DEGs was performed using Gene Ontology (GO) annotation. Validation of the result was performed by quantitative PCR using LSG from IgG4-RD (n=9), SS (n=10), and controls (n=4). &lt;Results&gt; Gene expression patterns in IgG4-RD, SS, and healthy controls were quite different with each other in hierarchical clustering as well as principal component analysis. In IgG4-RD, 1771 up-regulated probe sets (corresponding to 1321 up-regulated genes) and 1785 down-regulated probe sets (corresponding to 1320 down-regulated genes) were identified as DEGs (false discovery rate &lt;0.05). GO term analysis indicated that the up-regulated set of DEGs in IgG4-RD encoded proteins that function in cell proliferation, extracellular matrix organization, and organ development. PCR validated significantly higher expression of lactotransferrin (LTF) in IgG4-RD than SS (P&lt;0.05), and chemokine (C-C motif) ligand 18 (CCL18) in IgG4-RD than SS and controls (P&lt;0.05). &lt;Conclusion&gt; The results clearly showed that the gene expression pattern in LSG of IgG4-RD is different from that of SS.  LSG samples were collected from 5 Japanese patients with IgG4-RD, as well as from 5 Japanese patients with SS who had been followed up at University of Tsukuba Hospital (Ibaraki, Japan). All patients with IgG4-RD satisfied the comprehensive diagnostic criteria for IgG4-related disease (IgG4-RD) 2011 proposed by the All Japan IgG4 team [3]. The diagnosis of IgG4-RD was based on the presence of all three items; 1) clinical examination showing characteristic diffuse/localized swelling or masses in single or multiple organs, 2) Hematological examination shows elevated serum IgG4 concentrations (135 mg/dl), 3) Histopathologic examination shows: (1) Marked lymphocyte and plasmacyte infiltration and fibrosis. (2) Infiltration of IgG4+ plasma cells: ratio of IgG4+/IgG+ cells &gt; 40% and &gt;10 IgG4+ plasma cells/HPF. All patients with SS satisfied the Japanese Ministry of Health criteria for the diagnosis of SS (1999) [4]. These criteria included four clinicopathological findings: lymphocytic infiltration of the salivary or lacrimal glands, dysfunction of salivary secretion, keratoconjunctivitis sicca, and presence of anti-SS-A or SS-B antibodies. The diagnosis of SS was based on the presence of two or more of the above four items. Approval for this study was obtained from the local ethics committee and a signed informed consent was obtained from each subject.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-40568</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-40568/samples/</item></data></biogps>
