<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Ji H</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To study the mechanism by which conditioned medium of bone marrow mesenchymal stem cells (BMSCs-CM) facilitates the transition of pro-inflammatory polarized microglia to an anti-inflammatory phenotype.&lt;h4>Methods&lt;/h4>BV2 cells, a mouse microglia cell line, were transformed into a pro-inflammatory phenotype using lipopolysaccharide. The expression of phenotypic genes in BV2 cells was detected using real-time quantitative PCR (RT-qPCR). Enzyme-linked immunosorbent assay was used to measure inflammatory cytokine levels in BV2 cells co-cultured with BMSCs-CM. The expressions of mitophagy-associated proteins were determined using western blot. The mitochondrial membrane potential and ATP levels in BV2 cells were measured using JC-1 staining and an ATP assay kit, respectively. </pubmed_abstract><journal>PeerJ</journal><pagination>e17664</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11227809</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Conditioned culture medium of bone marrow mesenchymal stem cells promotes phenotypic transformation of microglia by regulating mitochondrial autophagy.</pubmed_title><pmcid>PMC11227809</pmcid><pubmed_authors>Peng X</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Ji H</pubmed_authors><pubmed_authors>Chu W</pubmed_authors><pubmed_authors>Song X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conditioned culture medium of bone marrow mesenchymal stem cells promotes phenotypic transformation of microglia by regulating mitochondrial autophagy.</name><description>&lt;h4>Objective&lt;/h4>To study the mechanism by which conditioned medium of bone marrow mesenchymal stem cells (BMSCs-CM) facilitates the transition of pro-inflammatory polarized microglia to an anti-inflammatory phenotype.&lt;h4>Methods&lt;/h4>BV2 cells, a mouse microglia cell line, were transformed into a pro-inflammatory phenotype using lipopolysaccharide. The expression of phenotypic genes in BV2 cells was detected using real-time quantitative PCR (RT-qPCR). Enzyme-linked immunosorbent assay was used to measure inflammatory cytokine levels in BV2 cells co-cultured with BMSCs-CM. The expressions of mitophagy-associated proteins were determined using western blot. The mitochondrial membrane potential and ATP levels in BV2 cells were measured using JC-1 staining and an ATP assay kit, respectively. </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-26T05:42:01.557Z</modification><creation>2025-04-06T11:36:45.606Z</creation></dates><accession>S-EPMC11227809</accession><cross_references><pubmed>38974415</pubmed><doi>10.7717/peerj.17664</doi></cross_references></HashMap>