<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">2244</item><item key="factors"><item><item key="GSM1062207"><item key="TREATMENT PROTOCOL">stimulation with aNKp44 and IL-1/IL-7/IL-23</item></item></item><item><item key="GSM1062207"><item key="TREATMENT PROTOCOL">stimulation with aNKp44 and IL-1/IL-7/IL-23</item></item></item><item><item key="GSM1062207"><item key="TREATMENT PROTOCOL">stimulation with aNKp44 and IL-1/IL-7/IL-23</item></item></item><item><item key="GSM1062204"><item key="TREATMENT PROTOCOL">stimulation with aNKp44</item></item></item><item><item key="GSM1062204"><item key="TREATMENT PROTOCOL">stimulation with aNKp44</item></item></item><item><item key="GSM1062204"><item key="TREATMENT PROTOCOL">stimulation with aNKp44</item></item></item><item><item key="GSM106220"><item key="TREATMENT PROTOCOL">stimulation with IL-1/IL-7/IL-23</item></item></item><item><item key="GSM106220"><item key="TREATMENT PROTOCOL">stimulation with IL-1/IL-7/IL-23</item></item></item><item><item key="GSM106220"><item key="TREATMENT PROTOCOL">stimulation with IL-1/IL-7/IL-23</item></item></item><item><item key="GSM1062198"><item key="TREATMENT PROTOCOL">ex-vivo</item></item></item><item><item key="GSM1062198"><item key="TREATMENT PROTOCOL">ex-vivo</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">ROR&#947;t+ innate lymphoid cells (ILC) are crucial players of innate immune responses and represent a major source of IL-22, which has an...</item><item key="pubmed_id">23791642</item><item key="geo_gse_id">E-GEOD-43409</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">11</item><item key="tags"><item>cytokine</item><item>tonsil</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">rort-innate-lymphoid-cells-transcriptomes-after-an</item><item key="geo_id_plat">E-GEOD-43409_A-AFFY-44</item><item key="name">ROR&#947;t+ Innate lymphoid cells transcriptomes after aNKp44 and cytokine stimulation</item><item key="created">Jul.11, 2014</item><item key="summary">ROR&#947;t+ innate lymphoid cells (ILC) are crucial players of innate immune responses and represent a major source of IL-22, which has an important role in mucosal homeostasis. The signals required by ROR&#947;t+ ILC to express IL-22 and other cytokines, including TNF, have only partially been elucidated. Here we show that ROR&#947;t+ ILC can directly sense the environment by the engagement of the activating receptor NKp44. NKp44 triggering in ROR&#947;t+ ILC selectively activates a coordinated pro-inflammatory program, including TNF, while cytokine stimulation induces preferentially IL-22 expression. However, combined engagement of NKp44 and cytokine receptors results in a strong synergistic effect. These data support the concept that NKp44+ ROR&#947;t+ ILC can be activated without cytokines and are able to switch between IL-22 or TNF production, depending on the triggering stimulus. Transcriptome analysis of CD56+CD127hi tonsil ILC, Ex vivo and after stimulation with aNKp44, IL-1/IL-7/IL-23 or aNKp44/IL-1/IL-7/IL-23 for 3.5h. RNA was extracted and pooled from 2 donors each, Amplified and labeled according to manufacturer&#180;s instructions (GeneChipU133plus2&#174; , Affymetrix). The analysis was performed in triplicates.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-43409</item><item key="species">human</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-43409/samples/</item></data></biogps>
