<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park DJ</submitter><funding>American Heart Association</funding><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><pagination>2831-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2877844</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>176(6)</volume><pubmed_abstract>Heme oxygenase-1 (HO-1) is a microsomal enzyme with antioxidant, antiapoptotic, and immunoregulatory functions. We studied the expression of HO-1 by bone marrow-derived dendritic cells (BMDCs) and splenic DC subpopulations under quiescent conditions or following lipopolysaccharide (LPS) stimulation. The kinetics of HO-1 expression by BMDCs depended on the conditions under which they were propagated. Expression of HO-1 in mouse BMDCs in 100 U/ml GM-CSF peaked at 16 hours after LPS treatment and maintained expression for at least 48 hours. But cultures in 800 U/ml granulocyte-macrophage colony-stimulating factor (GM-CSF) showed peak expression by 16 hours that disappeared by 48 hours after LPS stimulation, similar to BMDCs cultured in both 100 U/ml GM-CSF and IL-4 (10 ng/ml). By flow cytomet</pubmed_abstract><journal>The American journal of pathology</journal><pubmed_title>Heme oxygenase-1 expression in murine dendritic cell subpopulations: effect on CD8+ dendritic cell differentiation in vivo.</pubmed_title><pmcid>PMC2877844</pmcid><funding_grant_id>R01 DK059600</funding_grant_id><funding_grant_id>0655318B</funding_grant_id><funding_grant_id>DK59600</funding_grant_id><funding_grant_id>P30 DK 079337</funding_grant_id><funding_grant_id>DK 079337</funding_grant_id><funding_grant_id>P30 DK079337</funding_grant_id><funding_grant_id>DK75332</funding_grant_id><pubmed_authors>Agarwal A</pubmed_authors><pubmed_authors>George JF</pubmed_authors><pubmed_authors>Park DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heme oxygenase-1 expression in murine dendritic cell subpopulations: effect on CD8+ dendritic cell differentiation in vivo.</name><description>Heme oxygenase-1 (HO-1) is a microsomal enzyme with antioxidant, antiapoptotic, and immunoregulatory functions. We studied the expression of HO-1 by bone marrow-derived dendritic cells (BMDCs) and splenic DC subpopulations under quiescent conditions or following lipopolysaccharide (LPS) stimulation. The kinetics of HO-1 expression by BMDCs depended on the conditions under which they were propagated. Expression of HO-1 in mouse BMDCs in 100 U/ml GM-CSF peaked at 16 hours after LPS treatment and maintained expression for at least 48 hours. But cultures in 800 U/ml granulocyte-macrophage colony-stimulating factor (GM-CSF) showed peak expression by 16 hours that disappeared by 48 hours after LPS stimulation, similar to BMDCs cultured in both 100 U/ml GM-CSF and IL-4 (10 ng/ml). By flow cytomet</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-04T11:31:38.488Z</modification><creation>2019-03-27T00:31:08Z</creation></dates><accession>S-EPMC2877844</accession><cross_references><pubmed>20395442</pubmed><doi>10.2353/ajpath.2010.090845</doi></cross_references></HashMap>