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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">mouse</item><item key="factors"><item><item key="GSM571000"><item key="DENDRITIC CELL">CD8+CX3CR1+</item></item></item><item><item key="GSM571000"><item key="DENDRITIC CELL">CD8+CX3CR1+</item></item></item><item><item key="GSM571002"><item key="DENDRITIC CELL">CD4+</item></item></item><item><item key="GSM571002"><item key="DENDRITIC CELL">CD4+</item></item></item></item><item key="id">6172</item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">We describe a novel subset of CD8+ DCs in lymphoid organs of na&#239;ve mice characterized by expression of the CX3CR1 chemokine receptor....</item><item key="pubmed_id">20679228</item><item key="geo_gse_id">E-GEOD-23212</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">4</item><item key="tags"><item>chemokine</item><item>genome</item><item>immunoglobulin</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-profiling-of-mouse-splenic-dendrit</item><item key="geo_id_plat">E-GEOD-23212_A-AFFY-45</item><item key="name">Gene expression profiling of mouse splenic Dendritic cells subsets</item><item key="created">Nov.11, 2014</item><item key="summary">We describe a novel subset of CD8+ DCs in lymphoid organs of na&#239;ve mice characterized by expression of the CX3CR1 chemokine receptor. CX3CR1+CD8+ DCs lack hallmarks of classical CD8+ DCs, including IL12 secretion, the capacity to cross-present antigen and their developmental independence of the transcriptional factor BatF3. Gene expression profiling showed that CX3CR1+CD8+ DCs resemble CD8- cDCs. The microarray analysis further revealed a unique plasmacytoid DC (PDC) gene signature of CX3CR1+ CD8+ DCs. A PDC relationship of the cells is further supported by the fact that they harbor characteristic D-J immunoglobulin gene rearrangements and that development of CX3CR1+CD8+ DCs requires E2-2, the critical transcriptional regulator of PDCs. Thus, CX3CR1+ CD8+ DCs represent a unique DC subset, related to but distinct from PDCs. After collagenase D digestion, spleens from Cx3cr1gfp/+ C57BL/6 mice were enriched for CD11c+ cells by magnetic separation according to the manufacturer&#8217;s protocol (MiltenyiBiotec GmbH). Splenic CD11chi cells were isolated using the FACS ARIA high-speed sorter (Becton-Dickinson). Total RNA was extracted and subjected to gene expression profiling using the Mouse Genome 430.2 Affymetrix GeneChip</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23212</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-23212/samples/</item></data></biogps>
