<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(7)</volume><submitter>Zou Y</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Mast cells-derived extracellular vesicles (EVs) play vital roles in various physiological and pathophysiological conditions. However, the cargoes of mast cells-derived EVs in asthma have not been established. Here, we set to identify the role of microRNA-21 (miRNA-21) from mast cells-derived EVs in ozone- and lipopolysaccharide (LPS)-induced mouse airway epithelial cells (MIC-iCell-a006 cells) and asthmatic mice.&lt;h4>Methods&lt;/h4>After ozone or LPS treatment, MIC-iCell-a006 cells were subjected to a microarray analysis to screen differentially expressed miRNAs, and then co-cultured with EVs. miR-21 was silenced in cells, followed by CCK-8, scratch, and Transwell assays. Mice were challenged with ovalbumin, and antioxidant enzymes and inflammatory cell infiltration were asse</pubmed_abstract><journal>American journal of translational research</journal><pagination>7475-7491</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8340267</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MicroRNA-21 released from mast cells-derived extracellular vesicles drives asthma in mice by potentiating airway inflammation and oxidative stress.</pubmed_title><pmcid>PMC8340267</pmcid><pubmed_authors>Zou Y</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>MicroRNA-21 released from mast cells-derived extracellular vesicles drives asthma in mice by potentiating airway inflammation and oxidative stress.</name><description>&lt;h4>Objective&lt;/h4>Mast cells-derived extracellular vesicles (EVs) play vital roles in various physiological and pathophysiological conditions. However, the cargoes of mast cells-derived EVs in asthma have not been established. Here, we set to identify the role of microRNA-21 (miRNA-21) from mast cells-derived EVs in ozone- and lipopolysaccharide (LPS)-induced mouse airway epithelial cells (MIC-iCell-a006 cells) and asthmatic mice.&lt;h4>Methods&lt;/h4>After ozone or LPS treatment, MIC-iCell-a006 cells were subjected to a microarray analysis to screen differentially expressed miRNAs, and then co-cultured with EVs. miR-21 was silenced in cells, followed by CCK-8, scratch, and Transwell assays. Mice were challenged with ovalbumin, and antioxidant enzymes and inflammatory cell infiltration were asse</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-06-01T03:30:08.682Z</modification><creation>2025-06-01T03:30:08.682Z</creation></dates><accession>S-EPMC8340267</accession><cross_references><pubmed>34377230</pubmed></cross_references></HashMap>