<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM989635"><item key="IFN TYPE1">IFN&#945;1-DC</item></item></item><item><item key="GSM989636"><item key="IFN TYPE1">IFN&#945;2-DC</item></item></item><item><item key="GSM989637"><item key="IFN TYPE1">IFN&#945;8-DC</item></item></item><item><item key="GSM989638"><item key="IFN TYPE1">IFN&#945;21-DC</item></item></item><item><item key="GSM989639"><item key="IFN TYPE1">IFN&#946;-DC</item></item></item></item><item key="id">4556</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Type I interferon (IFN) is a family of 15 cytokines (in human 13&#945;, 1&#946;,1&#969;) which exert several cellular functions through the binding to a...</item><item key="geo_gse_id">E-GEOD-40268</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">5</item><item key="tags"><item>cell</item><item>surface</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-data-from-5-ifn-type-i-derived-dendriti</item><item key="geo_id_plat">E-GEOD-40268_A-AFFY-44</item><item key="name">Expression data from 5 IFN type I-derived Dendritic Cells</item><item key="created">Sep.19, 2014</item><item key="summary">Type I interferon (IFN) is a family of 15 cytokines (in human 13&#945;, 1&#946;,1&#969;) which exert several cellular functions through the binding to a common receptor. Despite the initial activation of the same Jak/Stat signalling pathway, the cellular response may be different depending on the type I IFN subtype. We investigated the activity of different type I IFN subtypes - IFN&#945;1, &#945;2, &#945;8, &#945;21, &#969; and &#946;- on the differentiation of DC. Transcriptome analyses identified two distinct groups, the IFN&#945;/&#969;-DC and the IFN&#946;-DC. 78 genes, 7 chemokines and expression levels of cell surface markers characteristic of DC distinguished IFN&#945;-DC and IFN&#946;-DC. These differences are unlikely to impact the efficacy of T cell functional response since IFN&#945;2-DC and IFN&#946;-DC were equipotent in inducing the proliferation and the polarization of allogenic na&#239;ve CD4 T cells into Th1 cells and in stimulating autologous memory CD4 or CD8 T cells. In contrast, IFN&#945;2-DC were found to be more efficient than IFN&#946;-DC in the phagocytic uptake of dead cells. Human blood monocytes were differentiated in DC by using 5 differents IFN type I (IFN&#945;2, &#945;1, &#945;8, &#945;21 and &#946;). After 3 days of differentiation RNA were extracted and analyzed by affymetrix microarray.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-40268</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-40268/samples/</item></data></biogps>
