<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Manuela Garcia-Canovas</submitter><organism>Sus scrofa</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15241</full_dataset_link><description>This study explores the biological role of interleukin-6 (IL-6) as a supplement during in vitro maturation (IVM) of porcine oocytes, aiming to enhance embryonic development and reduce apoptosis following in vitro fertilization (IVF). The objective was to determine whether IL-6 supplementation alters gene expression in day-7 in vitro-produced blastocysts. To achieve this, oocytes from prepubertal gilts were matured in IVM medium with or without 100 ng/mL IL-6, fertilized in vitro, and cultured for seven days. Viable blastocysts were collected, flash-frozen, and analyzed using the GeneChip® Porcine Genome Array to identify differentially expressed genes (DEGs). The results revealed significant upregulation of genes involved in lipid metabolism, cell proliferation, immune response, and embryo development in the IL-6 group, highlighting IL-6’s potential to improve oocyte developmental competence through modulation of key biological pathways.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Culture of morulae was performed for 24 h in NCSU-23 medium supplemented with 0.3 mg/mL PVA and 100 ng/mL platelet factor-4 under a paraffin oil cover</sample_protocol><sample_protocol>Sample Treatment - The oocytes from prepubertal gilts were collected and matured in IVM medium either supplemented with 100 ng/mL IL-6 or without supplementation</sample_protocol><sample_protocol>Labeling - The ds-DNA targets were purified, fragmented and terminally labeled.</sample_protocol><sample_protocol>Sample Collection - Samples are a pool of 7 viable in vitro produced porcine blastocysts obtained from oocytes matured in vitro in the presence or abscense of interleukin 6.</sample_protocol><sample_protocol>Scaning - Affymetrix Expression Command Console (Affymetrix.Intensity data from each GeneChip® array were normalized using the robust multiarray mean (RMA) method.</sample_protocol><sample_protocol>Hybridization - A total of 4.5 µg of the fragmented and biotinylated ds-DNA was incorporated into a hybridization mix from a GeneChip Hybridization, Wash and Stain Kit (P/N 90720; Affymetrix).</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNeasy Micro Kit (P/N 74004; Qiagen Iberica, Madrid, Spain) was used to extract total RNA.</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><data_protocol>Data Transformation - The raw data were transformed using the log2 function and then normalize using quantile methods to derive individual intensity values.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><study_type>transcription profiling by array</study_type><species>Sus scrofa</species><pubmed_title>Exposure of in vitro maturing pig oocytes to exogenous interleukin-6 modulates transcriptome profiles of resulting blastocysts, upregulating developmental signaling pathways</pubmed_title><pubmed_authors>Manuela Garcia-Canovas</pubmed_authors><pubmed_authors>Manuela Garcia-Canovas, Adelina Lopez-Jara, Inmaculada Parrilla, Alejandro Gonzalez-Plaza, Heriberto Rodriguez-Martinez, Maria A. Gil, Cristina Cuello, Emilio A. Martinez</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptome profile of in vitro produced blastocysts derived from in vitro matured oocytes exposed to exogenous interleukin-6</name><description>This study explores the biological role of interleukin-6 (IL-6) as a supplement during in vitro maturation (IVM) of porcine oocytes, aiming to enhance embryonic development and reduce apoptosis following in vitro fertilization (IVF). The objective was to determine whether IL-6 supplementation alters gene expression in day-7 in vitro-produced blastocysts. To achieve this, oocytes from prepubertal gilts were matured in IVM medium with or without 100 ng/mL IL-6, fertilized in vitro, and cultured for seven days. Viable blastocysts were collected, flash-frozen, and analyzed using the GeneChip® Porcine Genome Array to identify differentially expressed genes (DEGs). The results revealed significant upregulation of genes involved in lipid metabolism, cell proliferation, immune response, and embryo development in the IL-6 group, highlighting IL-6’s potential to improve oocyte developmental competence through modulation of key biological pathways.</description><dates><release>2025-06-30T00:00:00Z</release><modification>2025-06-18T15:26:31.766Z</modification><creation>2025-06-18T15:26:31.766Z</creation></dates><accession>E-MTAB-15241</accession><cross_references><EFO>EFO_0002768</EFO><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>