<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Haibo Qiu</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0006661000</full_dataset_link><submitter_email>haiboq2000@163.com</submitter_email><submitter_affiliation>Jiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>The role of endothelial cell-derived extracellular vesicles in acute respiratory distress syndrome</name><description>Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a common life-threatening critical syndrome with no effective pharmacotherapy. Extracellular vesicles (EVs) are considered as a new way of long-distance communication between cells. Our previous research using an ex vivo perfused human ALI model suggested that endothelial cell-derived EVs (EC-EVs) mediate the development of ALI/ARDS. However, how EC-EVs aggravate lung injury remains largely unknown. Here we demonstrated that EC-EVs released under inflammatory stimulation can lead to ALI, and the proteomic analysis was performed on EC-EVs to explore the mechanism.</description><dates><publication>Mon Jul 03 00:00:00 GMT+01:00 2023</publication></dates><accession>PXD043470</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>