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Köhler, A. ; Geiselhöringer, A.-L. ; Kolland, D. ; Kreft, L. ; Wichmann, N. ; Hils, M.* ; Szente-Pasztoi, M. ; Zurkowski, E.* ; Vogt, J.* ; Kübelbeck, T.* ; Biedermann, T.* ; Schmitz, I.* ; Hansen, W.* ; Kramer, D.* ; Gaida, M.M.* ; Schmidt-Weber, C.B. ; Hoevelmeyer, N.* ; Ohnmacht, C.

The atypical IκB family member Bcl3 determines differentiation and fate of intestinal RORγt+ regulatory T cell subsets.

Mucosal Immunol. 17, 673-691 (2024)
Verlagsversion DOI PMC
Open Access Hybrid
Creative Commons Lizenzvertrag
Peripherally induced regulatory T cells (pTregs) expressing the retinoic acid receptor-related orphan-receptor gamma t (RORγt) are indispensable for intestinal immune homeostasis. NF-κB family members regulate the differentiation of thymic Tregs and promote their survival in the periphery. However, the Treg-intrinsic molecular mechanisms controling the size of the pTregs in the intestine and associated lymphoid organs remain unclear. Here, we provide direct evidence that Bcl3 limits the development of pTregs in a T cell-intrinsic manner. Moreover, the absence of Bcl3 allowed for the formation of an unusual intestinal Treg population co-expressing the transcription factors Helios and RORγt. The expanded RORγt+ Treg populations in the absence of Bcl3 displayed an activated phenotype and secreted high levels of the anti-inflammatory cytokines IL-10 and TGFβ. They were fully capable of suppressing effector T cells in a transfer colitis model despite an intrinsic bias to trans-differentiate toward Th17-like cells. Finally, we provide a Bcl3-dependent gene signature in pTregs including altered responsiveness to the cytokines IL-2, IL-6, and TNFα. Our results demonstrate that Bcl3 acts as a molecular switch to limit the expansion of different intestinal Treg subsets and may thus serve as a novel therapeutic target for inflammatory bowel disease by restoring intestinal immune tolerance.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Bcl3 ; Foxp3 ; Intestinal Tolerance ; Nf- κb ; Ror Gamma T ; Inflammatory Bowel Disease ; Regulatory T Cells; Proprotein Convertase Furin; Tolerance; Oncoprotein; Plasticity; Immunity; Receptor; Therapy; Lineage; Binding; Stat3
Sprache englisch
Veröffentlichungsjahr 2024
HGF-Berichtsjahr 2024
ISSN (print) / ISBN 1933-0219
e-ISSN 1933-0219
Zeitschrift Mucosal Immunology
Quellenangaben Band: 17, Heft: 4, Seiten: 673-691 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort UNITED STATES
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Allergy Research (IAF)
POF Topic(s) 30202 - Environmental Health
30503 - Chronic Diseases of the Lung and Allergies
Forschungsfeld(er) Allergy
PSP-Element(e) G-505400-001
G-505491-001
G-509000-006
Förderungen German Research Foundation
European Research Council (ERC)
DOI 10.1016/j.mucimm.2024.04.002
WOS ID 001294028700001
Scopus ID 85192137838
PubMed ID 38663461
Erfassungsdatum 2024-06-10
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