<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Lian Ma</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018185000</full_dataset_link><submitter_email>malian8965@sina.com</submitter_email><submitter_affiliation>West China Second Hospital of Sichuan University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Advantages of Pooled-Donor Culture of Foreskin Mesenchymal Stromal Cells for Extracellular Vesicle Production: Insights from Multi-Omics Analysis</name><description>This project characterizes the proteomic landscape of small extracellular vesicles (sEVs) derived from human adipose-, foreskin-, and umbilical cord-derived mesenchymal stromal cells (MSCs) cultured under single-donor or pooled-donor conditions in conventional 2D culture and 3D microcarrier-based bioreactors. DIA-based quantitative proteomics was used to determine how donor pooling and 3D culture reshape sEV cargo composition, reduce batch-level heterogeneity, and establish conserved protein signatures across tissue sources. The dataset identifies manufacturing-responsive molecular programs related to mitophagy, immune communication, phagocytosis, membrane repair, wound healing, and mitochondrial metabolism. Foreskin-derived MSC-sEVs showed the strongest response to pooled-donor and 3D culture conditions, supporting their potential as a platform for engineered immuno-mitochondrial and reparative vesicle products.</description><dates><publication>Sun Jul 05 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD080621</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>