<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Pei Zhang</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0017329000</full_dataset_link><submitter_email>zhangpei@ahmu.edu.cn</submitter_email><submitter_affiliation>Department of Nephrology, The First Affiliated Hospital of Anhui Medical University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Proteomic profiling of extracellular vesicles (EVs) isolated from peritoneal dialysis effluent (PDE) of short-term (SPD) and long-term (LPD) PD patients</name><description>This project presents proteomic profiling of extracellular vesicles (EVs) isolated from peritoneal dialysis effluent (PDE) of short-term (SPD) and long-term (LPD) PD patients. We identified 536 differentially expressed proteins (DEPs), revealing an immune-enriched EV signature in LPD. CSF1 was prioritized as a key profibrotic mediator, validated in vitro and in vivo to drive macrophage-to-myofibroblast transition (MMT) via AKT signaling. Clinical data (n=84) links dialysate CSF1 to PF progression. This dataset provides mechanistic insights and biomarker candidates for PD-related fibrosis.</description><dates><publication>Sat May 23 00:00:00 BST 2026</publication></dates><accession>PXD078788</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>