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Memorial Sloan Kettering Cancer Center"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA329604"],"scientific_name":["Mus musculus"],"long_description":["Regulatory T (Treg) cells, expressing abundant amounts of the IL-2 receptor (IL-2R), are reliant on IL-2 produced by activated T cells. This feature implied a key role for a simple network based on IL-2 consumption by Treg cells in their suppressor function. However, congenital deficiency in IL-2R results in reduced expression of the Treg lineage specification factor Foxp3, confounding experimental efforts to understand the role of IL-2R expression and signaling in Treg suppressor function. Using genetic gain and loss of function approaches, we demonstrate that IL-2 capture is dispensable for control of CD4+ T cells, but is important for limiting CD8+ T cell activation, and that IL-2R dependent STAT5 transcription factor activation plays an essential role in Treg suppressor function separable from T cell receptor signaling. Overall design: Gene expression profiles in Treg cells with or without an expression of an active form of STAT5 were compared by RNA sequencing. Male 8-wk-old Foxp3Cre-ERT2Rosa26Stat5bCA (STAT5b-CA) and Foxp3Cre-ERT2 (control) mice, nine mice for each experimental group, received a single dose (4 mg) of tamoxifen by oral gavage 4 months before isolation. Splenic CD4+Foxp3(YFP/GFP)+GITRhiCD25hi Treg and CD4+Foxp3(YFP/GFP)-CD62LhiCD44lo T naive cells were double sorted using a BD FACSAria II cell sorter. The T cell subsets isolated from three individual mice in the same experimental group (genotype) was pooled into one biological replicate three biological replicates were generated. A total of 12 samples, i.e., two genotypes, two cell cypes, and three replicates, was subjected to RNA-seq analysis. Samples were sequenced on the Illumina HiSeq 2500 to an average depth of 27.5 million 50-bp read pairs per sample."],"tag":["xref:PubMed:30643266","xref:PubMed:27595233"],"repository":["ENA"],"description_synonyms":["Thymocyte Stimulating Factor, Treg cell, Suppressor T Cells, Regulatory, Regulatory T-Cell, Il-2, Naturally-Occurring Suppressor T-Lymphocytes, Regulatory T-Lymphocyte, Regulatory T-Lymphocytes, Naturally-Occurring Suppressor T-Cell, Suppressor T-Lymphocytes, T-Lymphocyte, Regulatory T, Suppressor T-Cell, Cell, Th3, T Cell Growth Factor, Concept, Regulatory T Cell, Role Concept, Ro-23-6019, Interleukin II, TCGF, Roles, IL-2, T-Cell, T suppressor cell, Ro 23 6019, Role, Concepts, Naturally-Occurring Suppressor T-Cells, Naturally-Occurring Suppressor T-Lymphocyte, Regulatory T Cells, Th3 Cells, Th3 Cell, RU-49637, lymphokine, Suppressor T-Cells, Suppressor T Lymphocytes, Naturally Occurring., Interleukine 2, interleukin-2 receptor ligand, Aldesleukin, Tr1 Cell, aldesleukin, Suppressor T-Lymphocyte, Ro 236019, Mitogenic Factor, T-Cells, RU49637, Tr1, Ro-236019, T-Cell Growth Factor, Interleukin 2, Regulatory T Lymphocytes, Treg Cells, Treg Cell, regulatory T-cell, Lymphocyte Mitogenic Factor, Naturally-Occurring Suppressor, Naturally Occurring, suppressor T-cell, Tr1 Cells, T Cells, suppressor T-lymphocyte, Regulatory T Lymphocyte, Treg, T-cell growth factor, Regulatory T-Cells, Role Concepts, IL2, Ro236019, Cells, Naturally-Occurring, T-Cell Stimulating Factor, T Cell Stimulating Factor, T Cell, Ts cell, T Lymphocytes, RU 49637, Lymphocyte"],"name_synonyms":["Mus musculus, Laboratory Mice., House, Mus, Laboratory, Swiss, Mus domesticus, mouse, Mus musculus domesticus, Swiss Mouse, mouse <Mus musculus>, Mouse, House Mice, Swiss Mice, house mouse, Mice, Laboratory Mouse, House Mouse, mice C57BL/6xCBA/CaJ hybrid, domesticus, Mus muscaris"],"additional_accession":[]},"is_claimable":false,"name":"Mus musculus","description":"An essential role for the IL-2 receptor in Treg cell function","dates":{"last_updated":"2025-09-24","first_public":"2016-09-02"},"accession":"PRJNA329604","cross_references":{"GEO":["GSE84553"],"taxon":["10090"],"PubMed":["30643266","27595233"]}}