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<biogps><data><item key="platform">4</item><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM875816"><item key="growth condition">control</item></item></item><item><item key="GSM875816"><item key="growth condition">control</item></item></item><item><item key="GSM875816"><item key="growth condition">control</item></item></item><item><item key="GSM875816"><item key="growth condition">control</item></item></item><item><item key="GSM875820"><item key="growth condition">10% seminal plasma</item></item></item><item><item key="GSM875820"><item key="growth condition">10% seminal plasma</item></item></item><item><item key="GSM875820"><item key="growth condition">10% seminal plasma</item></item></item><item><item key="GSM875820"><item key="growth condition">10% seminal plasma</item></item></item><item><item key="GSM875824"><item key="growth condition">recombinant human TGF-beta 3 (5 nanogram per milliliter)</item></item></item><item><item key="GSM875824"><item key="growth condition">recombinant human TGF-beta 3 (5 nanogram per milliliter)</item></item></item><item><item key="GSM875824"><item key="growth condition">recombinant human TGF-beta 3 (5 nanogram per milliliter)</item></item></item><item><item key="GSM875824"><item key="growth condition">recombinant human TGF-beta 3 (5 nanogram per milliliter)</item></item></item></item><item key="id">4419</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-35830</item><item key="summary_wrapped">In this study we examined the influence of seminal plasma on gene expression in human Ect1 ectocervical epithelial cells, and the extent...</item><item key="pubmed_id">22706080</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">12</item><item key="tags"><item>cytokine</item><item>genome</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-by-array-of-human-ect1-ect</item><item key="geo_id_plat">E-GEOD-35830_A-AFFY-44</item><item key="name">Transcription profiling by array of human Ect1 ectocervical epithelials cells treated with seminal plasma or transforming growth factor-beta 3</item><item key="created">Sep.19, 2014</item><item key="summary">In this study we examined the influence of seminal plasma on gene expression in human Ect1 ectocervical epithelial cells, and the extent to which recombinant TGF&#946;3 elicits comparable changes. Ect1 cells were incubated with recombinant human TGF&#946;3 (5 ng/ml), 10% pooled human seminal plasma (v/v), or medium alone for 10h. RNA was reverse transcribed into cDNA and hybridized to Affymetrix GeneChip&#174; Human Genome U133 plus 2.0 microarrays (Affymetrix, Santa Clara, CA). Exposure of Ect1 cells to seminal plasma resulted in differential expression of a total of 3955 probe sets, identified using high stringency criteria with MAS 5.0 analysis. These corresponded to 1338 genes up-regulated and 1343 genes down-regulated by seminal plasma. TGF&#946;3 treatment of Ect1 cells resulted in differential expression of 884 probe sets, corresponding to 346 up-regulated genes and 229 down-regulated genes. The genes differentially regulated by seminal plasma included several genes associated with cytokine&#8211;cytokine receptor interaction, TGF&#946; signalling, JAK/STAT signalling or VEGF signalling pathways, as specified by the KEGG database. Of 47 genes in these families, 17 (36.1%) were similarly regulated by both seminal plasma and TGF&#946;3. These data, together with additional experiments showing all three TGF&#946; isoforms can regulate inflammatory cytokine expression in Ect1 cells, identify TGF&#946; isoforms as key agents in seminal plasma that signal induction of pro-inflammatory cytokine synthesis in cervical cells. RNA from each of four biological replicates, each comprising pooled material from separate sets of 4 replicate wells, was analysed for each treatment. Total RNA was reverse transcribed into cDNA and sent to the Australian Genome Research Facility (AGRF; Melbourne, Australia) for single-cycle labeling and hybridization to 12 Affymetrix GeneChip&#174; Human Genome U133 plus 2.0 microarrays (Affymetrix, Santa Clara, CA).</item><item key="geo_gse_id">E-GEOD-35830</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-35830/samples/</item></data></biogps>
