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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">5614</item><item key="factors"><item><item key="GSE14672GSM366044"/></item><item><item key="GSE14672GSM366045"/></item><item><item key="GSE14672GSM366046"/></item><item><item key="GSE14672GSM366047"/></item><item><item key="GSE14672GSM366048"/></item><item><item key="GSE14672GSM366049"/></item><item><item key="GSE14672GSM366050"/></item><item><item key="GSE14672GSM366051"/></item><item><item key="GSE14672GSM366052"/></item><item><item key="GSE14672GSM366053"/></item><item><item key="GSE14672GSM366054"/></item><item><item key="GSE14672GSM366055"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">GM-CSF controls the development of granulocytes but little is known about the contribution of the downstream mediating transcription...</item><item key="pubmed_id">19779039</item><item key="geo_gse_id">E-GEOD-14672</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">12</item><item key="tags"><item>cell</item><item>peripheral</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-mouse-wild-type-and-sta</item><item key="geo_id_plat">E-GEOD-14672_A-AFFY-45</item><item key="name">Transcription profiling of mouse wild type and Stat5a or 5b knock-out blood cells treated with GM-CSF to induce granulopoiesis</item><item key="created">Nov.10, 2014</item><item key="summary">GM-CSF controls the development of granulocytes but little is known about the contribution of the downstream mediating transcription factor STAT5A/B.  To elucidate this pathway, we generated mice lacking the Stat5a and 5b genes in blood cells.  Peripheral neutrophils were decreased and administration of 5-FU and GM-CSF failed to induce granulopoiesis in Stat5a/b-mutant mice. GMPs were isolated and cultured with GM-CSF.  Both the number and size of STAT5A/B-null colonies were reduced and GM-CSF-induced survival of mature STAT5A/B-null neutrophils was impaired.  Time-lapse cinematography and single cell tracking of GMPs revealed that STAT5A/B-null cells were characterized by a longer generation time and an increased cell death.  Gene expression profiling experiments suggested that STAT5A/B directs GM-CSF signaling through the regulation of cell survival genes. Experiment Overall Design: Mice lacking or with  the Stat5a and 5b genes in blood cells, which were treated w/o GMP</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-14672</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-14672/samples/</item></data></biogps>
