<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM859656"><item key="CELL LINE">OP9M2</item><item key="CELL TYPE">mesenchymal stem cell</item></item></item><item><item key="GSM859656"><item key="CELL LINE">OP9M2</item><item key="CELL TYPE">mesenchymal stem cell</item></item></item><item><item key="GSM859658"><item key="CELL LINE">BFC012</item><item key="CELL TYPE">Fibroblast from fetal liver</item></item></item><item><item key="GSM859658"><item key="CELL LINE">BFC012</item><item key="CELL TYPE">Fibroblast from fetal liver</item></item></item></item><item key="id">6747</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">One of the long-standing goals in the field has been to establish a culture system that would allow maintenance of HSC properties ex...</item><item key="geo_gse_id">E-GEOD-34973</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">4</item><item key="tags"><item>cell</item><item>genome</item><item>line</item><item>stem cell</item><item>stromal cell</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">gene-expression-data-from-the-mesenchymal-stem-cel</item><item key="geo_id_plat">E-GEOD-34973_A-AFFY-45</item><item key="name">Gene expression data from the mesenchymal stem cell line OP9M2 that supported expansion of human hematopoietic stem and progenitor cells in vitro</item><item key="created">Nov.12, 2014</item><item key="summary">One of the long-standing goals in the field has been to establish a culture system that would allow maintenance of HSC properties ex vivo. In the absence of such system, the ability to model human hematopoiesis in vitro has been limited, and there has been little progress in the expansion of human HSCs for clinical application. To that end, we defined a mesenchymal stem cell co-culture system based on a monoclonal OP9 stromal cell line (OP9M2), for expansion of clonally multipotent human HSPCs that were protected from apoptosis and immediate differentiation, and retained the HSPC phenotype. To identify the supportive mechanisms, we performed a genome-wide gene expression analysis of OP9M2 stromal cells and compared the expression to a non-supportive stomal line (BFC012). This co-culture system provides a new, well-defined platform for studying mechanisms involved in HSC-niche interactions and protection of critical HSC properties ex vivo. To determine the cellular identity and the supportive mechanism of the OP9M2 cells, we compared the OP9M2 cells with non-supportive BFC012 stromal cells using Affymetrix mouse microarrays.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-34973</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-34973/samples/</item></data></biogps>
