<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">7156</item><item key="factors"><item><item key="GSM1074697"><item key="TRANSDUCED WITH">adeno-EV (empty virus) at x100 MOI for 1h</item></item></item><item><item key="GSM1074698"><item key="TRANSDUCED WITH">adeno-Cre at x100 MOI for 1h</item></item></item><item><item key="GSM1074697"><item key="TRANSDUCED WITH">adeno-EV (empty virus) at x100 MOI for 1h</item></item></item><item><item key="GSM1074698"><item key="TRANSDUCED WITH">adeno-Cre at x100 MOI for 1h</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">PTEN is thought to play a critical role in T cell activation by negatively regulating the PI3K signaling pathway important for cellular...</item><item key="pubmed_id">23851688</item><item key="geo_gse_id">E-GEOD-43936</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>cell</item><item>cytokine</item><item>protein</item><item>thymus</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">evaluation-of-effect-of-pten-gene-deletion-in-mous</item><item key="geo_id_plat">E-GEOD-43936_A-AFFY-45</item><item key="name">Evaluation of effect of PTEN gene deletion in mouse CD4+ Th1 clones after stimulation</item><item key="created">Nov.12, 2014</item><item key="summary">PTEN is thought to play a critical role in T cell activation by negatively regulating the PI3K signaling pathway important for cellular activation, growth, and proliferation.  T cells from mice in which PTEN was conditionally deleted in the thymus were reported to display CD28-independent IL-2 production and relative resistance to anergy induction.  However, such observations could have stemmed from alterations in T cell development due to early deletion in thymocytes.  To directly eliminate PTEN in post-thymic T cells, we utilized CAR Tg x PTENflox/flox mice which enabled gene deletion using a Cre adenovirus in vitro.  Gene expression profiling revealed a small subset of induced genes that were augmented upon PTEN deletion and T cell stimulation.  Our results indicate that deletion of PTEN can augment the activation of post-thymic T cells.  Nonetheless, PTEN inhibition may be a viable target for immune potentiation due to increased cytokine production by activated CD4+ cells. It was of interest to determine the spectrum of transcripts regulated by PTEN using gene expression profiling.  To this end, CAR Tg x PTENflox/flox Th1 clones were either treated with adeno-Cre or adeno-EV, then confirmed to have PTEN protein abscence by western blot, then stimulated for 6 hours with anti-CD3/anti-CD28 mAb- coated beads and analyzed (2 total conditions). The experiment was replicated so there are 2 samples for each condition.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-43936</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-43936/samples/</item></data></biogps>
