Home > Publications database > Unveiling IRF4-steered regulation of context-dependent effector programs in CD4+ T cells under Th17- and Treg-skewing conditions. > print |
001 | 299791 | ||
005 | 20250316015809.0 | ||
024 | 7 | _ | |a 10.1016/j.celrep.2025.115407 |2 doi |
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041 | _ | _ | |a English |
082 | _ | _ | |a 610 |
100 | 1 | _ | |a Gabele, Anna |b 0 |
245 | _ | _ | |a Unveiling IRF4-steered regulation of context-dependent effector programs in CD4+ T cells under Th17- and Treg-skewing conditions. |
260 | _ | _ | |a Maryland Heights, MO |c 2025 |b Cell Press |
336 | 7 | _ | |a article |2 DRIVER |
336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1741876150_9597 |2 PUB:(DE-HGF) |
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520 | _ | _ | |a The transcription factor interferon regulatory factor 4 (IRF4) is crucial for the fate determination of pro-inflammatory T helper (Th) 17 and the functionally opposing group of immunomodulatory regulatory T (Treg) cells. However, the molecular mechanisms of how IRF4 steers diverse transcriptional programs in Th17 and Treg cells are far from being definitive. Here, we integrated data derived from affinity-purification and full mass-spectrometry-based proteome analysis with chromatin immunoprecipitation sequencing. This allowed the characterization of subtype-specific molecular programs and the identification of IRF4 interactors in the Th17/Treg context. Our data reveal that IRF4-interacting transcription factors are recruited to IRF composite elements for the regulation of cell-type-specific transcriptional programs as exemplarily demonstrated for FLI1, which, in cooperation with IRF4, promotes Th17-specific gene expression. FLI1 inhibition markedly impaired Th17 differentiation. The present 'omics' dataset provides a valuable resource for studying IRF4-mediated gene regulatory programs in pro- and anti-inflammatory immune responses. |
536 | _ | _ | |a 314 - Immunologie und Krebs (POF4-314) |0 G:(DE-HGF)POF4-314 |c POF4-314 |f POF IV |x 0 |
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650 | _ | 7 | |a CP: Immunology |2 Other |
650 | _ | 7 | |a ChIP-seq |2 Other |
650 | _ | 7 | |a FLI1 |2 Other |
650 | _ | 7 | |a IRF4 |2 Other |
650 | _ | 7 | |a Th17 cells |2 Other |
650 | _ | 7 | |a Treg cells |2 Other |
650 | _ | 7 | |a composite motif |2 Other |
650 | _ | 7 | |a protein-protein interaction |2 Other |
650 | _ | 7 | |a proteomics |2 Other |
700 | 1 | _ | |a Sprang, Maximilian |b 1 |
700 | 1 | _ | |a Cihan, Mert |b 2 |
700 | 1 | _ | |a Welzel, Mareen |b 3 |
700 | 1 | _ | |a Nurbekova, Assel |b 4 |
700 | 1 | _ | |a Romaniuk, Karolina |b 5 |
700 | 1 | _ | |a Dietzen, Sarah |b 6 |
700 | 1 | _ | |a Klein, Matthias |b 7 |
700 | 1 | _ | |a Bündgen, Georg |b 8 |
700 | 1 | _ | |a Emelianov, Maxim |b 9 |
700 | 1 | _ | |a Harms, Gregory |b 10 |
700 | 1 | _ | |a Rajalingam, Krishnaraj |b 11 |
700 | 1 | _ | |a Ziesmann, Tanja |b 12 |
700 | 1 | _ | |a Pape, Katrin |b 13 |
700 | 1 | _ | |a Wasser, Beatrice |b 14 |
700 | 1 | _ | |a Gomez-Zepeda, David |0 P:(DE-He78)4569ef2919d2438765ad71515f53646b |b 15 |u dkfz |
700 | 1 | _ | |a Braband, Kathrin |b 16 |
700 | 1 | _ | |a Delacher, Michael |b 17 |
700 | 1 | _ | |a Lemmermann, Niels |b 18 |
700 | 1 | _ | |a Bittner, Stefan |b 19 |
700 | 1 | _ | |a Andrade-Navarro, Miguel A |b 20 |
700 | 1 | _ | |a Tenzer, Stefan |0 P:(DE-He78)74e391c68d7926be83d679f3d8891e33 |b 21 |u dkfz |
700 | 1 | _ | |a Luck, Katja |b 22 |
700 | 1 | _ | |a Bopp, Tobias |b 23 |
700 | 1 | _ | |a Distler, Ute |b 24 |
773 | _ | _ | |a 10.1016/j.celrep.2025.115407 |g Vol. 44, no. 3, p. 115407 - |0 PERI:(DE-600)2649101-1 |n 3 |p 115407 |t Cell reports |v 44 |y 2025 |x 2211-1247 |
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