<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Yao S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Efficiently delivering nucleic acid into mammalian cells is essential to overexpress genes for assessing gene functions. Human bone marrow stem cells (hBMSCs) are the most studied tissue-derived stem cells. Adeno-associated viruses (AAVs) have been used to deliver DNA into hBMSCs for various purposes. Current literature reported that transduction efficiencies of up to 65% could be achieved by AAV gene delivery into hBMSCs. Further improvement of efficiency is needed and possible. This study tested a selection of AAV serotypes for high-efficient DNA delivery into hBMSCs.&lt;h4>Methods&lt;/h4>hBMSCs from different donors were infected with different serotypes of AAVs containing the enhanced green fluorescence protein (&lt;i>eGFP&lt;/i>) reporter gene driven by the CMV promoter. Green </pubmed_abstract><journal>Stem cell investigation</journal><pagination>3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9905037</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Optimization of adeno-associated virus (AAV) gene delivery into human bone marrow stem cells (hBMSCs).</pubmed_title><pmcid>PMC9905037</pmcid><pubmed_authors>Rong W</pubmed_authors><pubmed_authors>Yao S</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optimization of adeno-associated virus (AAV) gene delivery into human bone marrow stem cells (hBMSCs).</name><description>&lt;h4>Background&lt;/h4>Efficiently delivering nucleic acid into mammalian cells is essential to overexpress genes for assessing gene functions. Human bone marrow stem cells (hBMSCs) are the most studied tissue-derived stem cells. Adeno-associated viruses (AAVs) have been used to deliver DNA into hBMSCs for various purposes. Current literature reported that transduction efficiencies of up to 65% could be achieved by AAV gene delivery into hBMSCs. Further improvement of efficiency is needed and possible. This study tested a selection of AAV serotypes for high-efficient DNA delivery into hBMSCs.&lt;h4>Methods&lt;/h4>hBMSCs from different donors were infected with different serotypes of AAVs containing the enhanced green fluorescence protein (&lt;i>eGFP&lt;/i>) reporter gene driven by the CMV promoter. Green </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T18:43:59.637Z</modification><creation>2025-04-04T18:43:59.637Z</creation></dates><accession>S-EPMC9905037</accession><cross_references><pubmed>36761253</pubmed><doi>10.21037/sci-2022-042</doi></cross_references></HashMap>