<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen J</submitter><funding>Natural Science Foundation of Xinjiang Uygur Autonomous Region</funding><funding>Natural Science Foundation of Hunan Province</funding><funding>China Postdoctoral Science Foundation</funding><funding>National Natural Science Foundation of China</funding><pagination>295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10464265</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Acute lung injury (ALI), manifested as strong pulmonary inflammation and alveolar epithelial damage, is a life-threatening disease with high morbidity and mortality. Small extracellular vesicles (sEVs), secreted by multiple types of cells, are critical cellular communication mediators and can inhibit inflammation by transferring bioactive molecules, such as microRNAs (miRNAs). Thus, we hypothesized that sEVs derived from mesenchymal stromal cells (MSC sEVs) could transfer miRNAs to attenuate inflammation of lung epithelial cells during ALI.&lt;h4>Methods&lt;/h4>C57BL/6 male mice were intratracheally administered LPS (10 mg/kg). Six hours later, the mice were randomly administered with MSC sEVs (40 µg per mouse in 150 µl of saline), which were collected by ultracentrifugation. </pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Human umbilical cord mesenchymal stromal cell small extracellular vesicle transfer of microRNA-223-3p to lung epithelial cells attenuates inflammation in acute lung injury in mice.</pubmed_title><pmcid>PMC10464265</pmcid><funding_grant_id>81600063</funding_grant_id><funding_grant_id>2022M713520</funding_grant_id><funding_grant_id>2022D01C498</funding_grant_id><funding_grant_id>2017JJ3484</funding_grant_id><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Niu R</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zhu F</pubmed_authors><pubmed_authors>Pan P</pubmed_authors><pubmed_authors>Hao H</pubmed_authors><pubmed_authors>Luo B</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Human umbilical cord mesenchymal stromal cell small extracellular vesicle transfer of microRNA-223-3p to lung epithelial cells attenuates inflammation in acute lung injury in mice.</name><description>&lt;h4>Background&lt;/h4>Acute lung injury (ALI), manifested as strong pulmonary inflammation and alveolar epithelial damage, is a life-threatening disease with high morbidity and mortality. Small extracellular vesicles (sEVs), secreted by multiple types of cells, are critical cellular communication mediators and can inhibit inflammation by transferring bioactive molecules, such as microRNAs (miRNAs). Thus, we hypothesized that sEVs derived from mesenchymal stromal cells (MSC sEVs) could transfer miRNAs to attenuate inflammation of lung epithelial cells during ALI.&lt;h4>Methods&lt;/h4>C57BL/6 male mice were intratracheally administered LPS (10 mg/kg). Six hours later, the mice were randomly administered with MSC sEVs (40 µg per mouse in 150 µl of saline), which were collected by ultracentrifugation. </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2025-04-26T14:39:10.717Z</modification><creation>2025-04-06T14:37:42.994Z</creation></dates><accession>S-EPMC10464265</accession><cross_references><pubmed>37626408</pubmed><doi>10.1186/s12951-023-02038-3</doi></cross_references></HashMap>