<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Li J</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Induced pluripotent stem cells-derived exosomes (iPSCs-Exo) can effectively treat spinal cord injury (SCI) in mice. But the role of iPSCs-Exo in SCI mice and its molecular mechanisms remain unclear. This research intended to study the effects and molecular mechanism of iPSCs-Exo in SCI mice models. &lt;b>Methods:&lt;/b> The feature of iPSCs-Exo was determined by transmission electron microscope (TEM), nanoparticle tracking analysis (NTA), and western blot. The effects of iPSCs-Exo in the SCI mice model were evaluated by Basso Mouse Scale (BMS) scores and H&amp;E staining. The roles of iPSCs-Exo and miR-199b-5p in LPS-treated BMDM were verified by immunofluorescence, RT-qPCR, and Cytokine assays. The target genes of miR-199b-5p were identified, and the function of miR-199b-5p and i</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>1078761</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9871459</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Induced pluripotent stem cells as natural biofactories for exosomes carrying miR-199b-5p in the treatment of spinal cord injury.</pubmed_title><pmcid>PMC9871459</pmcid><pubmed_authors>Jing Y</pubmed_authors><pubmed_authors>Ali F</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Jia B</pubmed_authors><pubmed_authors>Jia Y</pubmed_authors><pubmed_authors>Yan Y</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Bai F</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Induced pluripotent stem cells as natural biofactories for exosomes carrying miR-199b-5p in the treatment of spinal cord injury.</name><description>&lt;b>Background:&lt;/b> Induced pluripotent stem cells-derived exosomes (iPSCs-Exo) can effectively treat spinal cord injury (SCI) in mice. But the role of iPSCs-Exo in SCI mice and its molecular mechanisms remain unclear. This research intended to study the effects and molecular mechanism of iPSCs-Exo in SCI mice models. &lt;b>Methods:&lt;/b> The feature of iPSCs-Exo was determined by transmission electron microscope (TEM), nanoparticle tracking analysis (NTA), and western blot. The effects of iPSCs-Exo in the SCI mice model were evaluated by Basso Mouse Scale (BMS) scores and H&amp;E staining. The roles of iPSCs-Exo and miR-199b-5p in LPS-treated BMDM were verified by immunofluorescence, RT-qPCR, and Cytokine assays. The target genes of miR-199b-5p were identified, and the function of miR-199b-5p and i</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-22T06:18:52.254Z</modification><creation>2025-04-05T21:41:26.357Z</creation></dates><accession>S-EPMC9871459</accession><cross_references><pubmed>36703756</pubmed><doi>10.3389/fphar.2022.1078761</doi></cross_references></HashMap>