<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(5)</volume><submitter>Cao X</submitter><pubmed_abstract>Muscle satellite cells (SCs) play a crucial role in the regeneration and repair of skeletal muscle injuries. Previous studies have shown that myogenic exosomes can enhance satellite cell proliferation, while the expression of miR-140-5p is significantly reduced during the repair process of mouse skeletal muscle injuries induced by BaCl2. This study aims to investigate the potential of myogenic exosomes carrying miR-140-5p inhibitors to activate SCs and influence the regeneration of injured muscles. Myogenic progenitor cell exosomes (MPC-Exo) and contained miR-140-5p mimics/inhibitors myogenic exosomes (MPC-Exo&lt;sup>140+&lt;/sup> and MPC-Exo&lt;sup>140-&lt;/sup>) were employed to treat SCs and use the model. The results demonstrate that miR-140-5p regulates SC proliferation by targeting &lt;i>Pax7&lt;/i>. Upon the addition of MPC-Exo and MPC-Exo&lt;sup>140-&lt;/sup>, &lt;i>Pax7&lt;/i> expression in SCs significantly increased, leading to the transition of the cell cycle from G1 to S phase and an enhancement in cell proliferation. Furthermore, the therapeutic effect of MPC-Exo&lt;sup>140-&lt;/sup> was validated in animal model, where the expression of muscle growth-related genes substantially increased in the gastrocnemius muscle. Our research demonstrates that MPC-Exo&lt;sup>140-&lt;/sup> can effectively activate dormant muscle satellite cells, initiating their proliferation and differentiation processes, ultimately leading to the formation of new skeletal muscle cells and promoting skeletal muscle repair and remodeling.</pubmed_abstract><journal>Aging</journal><pagination>4609-4630</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10968704</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Myogenic exosome miR-140-5p modulates skeletal muscle regeneration and injury repair by regulating muscle satellite cells.</pubmed_title><pmcid>PMC10968704</pmcid><pubmed_authors>Cao X</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Xue L</pubmed_authors><pubmed_authors>Luo X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Yan Y</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Yu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Myogenic exosome miR-140-5p modulates skeletal muscle regeneration and injury repair by regulating muscle satellite cells.</name><description>Muscle satellite cells (SCs) play a crucial role in the regeneration and repair of skeletal muscle injuries. Previous studies have shown that myogenic exosomes can enhance satellite cell proliferation, while the expression of miR-140-5p is significantly reduced during the repair process of mouse skeletal muscle injuries induced by BaCl2. This study aims to investigate the potential of myogenic exosomes carrying miR-140-5p inhibitors to activate SCs and influence the regeneration of injured muscles. Myogenic progenitor cell exosomes (MPC-Exo) and contained miR-140-5p mimics/inhibitors myogenic exosomes (MPC-Exo&lt;sup>140+&lt;/sup> and MPC-Exo&lt;sup>140-&lt;/sup>) were employed to treat SCs and use the model. The results demonstrate that miR-140-5p regulates SC proliferation by targeting &lt;i>Pax7&lt;/i>. Upon the addition of MPC-Exo and MPC-Exo&lt;sup>140-&lt;/sup>, &lt;i>Pax7&lt;/i> expression in SCs significantly increased, leading to the transition of the cell cycle from G1 to S phase and an enhancement in cell proliferation. Furthermore, the therapeutic effect of MPC-Exo&lt;sup>140-&lt;/sup> was validated in animal model, where the expression of muscle growth-related genes substantially increased in the gastrocnemius muscle. Our research demonstrates that MPC-Exo&lt;sup>140-&lt;/sup> can effectively activate dormant muscle satellite cells, initiating their proliferation and differentiation processes, ultimately leading to the formation of new skeletal muscle cells and promoting skeletal muscle repair and remodeling.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-04T23:52:53.942Z</modification><creation>2025-04-04T23:52:53.942Z</creation></dates><accession>S-EPMC10968704</accession><cross_references><pubmed>38428405</pubmed><doi>10.18632/aging.205617</doi></cross_references></HashMap>