<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sun J</submitter><funding>General Program of National Nature Science Foundation of China</funding><pagination>14</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7791667</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Exosomal microRNAs (miRs) derived from mesenchymal stem cells (MSCs) have been shown to play roles in the pathophysiological processes of sepsis. Moreover, miR-27b is highly enriched in MSC-derived exosomes. Herein, we aimed to investigate the potential role and downstream molecular mechanism of exosomal miR-27b in sepsis.&lt;h4>Methods&lt;/h4>Inflammation was induced in bone marrow-derived macrophages (BMDMs) by lipopolysaccharide (LPS), and mice were made septic by cecal ligation and puncture (CLP). The expression pattern of miR-27b in MSC-derived exosomes was characterized using RT-qPCR, and its downstream gene was predicted by in silico analysis. The binding affinity between miR-27b, Jumonji D3 (JMJD3), or nuclear factor κB (NF-κB) was characterized to identify the underly</pubmed_abstract><journal>Stem cell research &amp; therapy</journal><pubmed_title>microRNA-27b shuttled by mesenchymal stem cell-derived exosomes prevents sepsis by targeting JMJD3 and downregulating NF-κB signaling pathway.</pubmed_title><pmcid>PMC7791667</pmcid><funding_grant_id>81770028</funding_grant_id><pubmed_authors>Hu S</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Liao X</pubmed_authors><pubmed_authors>Qiu C</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Sun J</pubmed_authors></additional><is_claimable>false</is_claimable><name>microRNA-27b shuttled by mesenchymal stem cell-derived exosomes prevents sepsis by targeting JMJD3 and downregulating NF-κB signaling pathway.</name><description>&lt;h4>Background&lt;/h4>Exosomal microRNAs (miRs) derived from mesenchymal stem cells (MSCs) have been shown to play roles in the pathophysiological processes of sepsis. Moreover, miR-27b is highly enriched in MSC-derived exosomes. Herein, we aimed to investigate the potential role and downstream molecular mechanism of exosomal miR-27b in sepsis.&lt;h4>Methods&lt;/h4>Inflammation was induced in bone marrow-derived macrophages (BMDMs) by lipopolysaccharide (LPS), and mice were made septic by cecal ligation and puncture (CLP). The expression pattern of miR-27b in MSC-derived exosomes was characterized using RT-qPCR, and its downstream gene was predicted by in silico analysis. The binding affinity between miR-27b, Jumonji D3 (JMJD3), or nuclear factor κB (NF-κB) was characterized to identify the underly</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2025-04-18T14:42:20.164Z</modification><creation>2021-02-20T20:45:58Z</creation></dates><accession>S-EPMC7791667</accession><cross_references><pubmed>33413595</pubmed><doi>10.1186/s13287-020-02068-w</doi></cross_references></HashMap>