孤儿受体
核受体
RAR相关孤儿受体γ
维甲酸
细胞分化
免疫系统
生物
免疫学
人口
FOXP3型
遗传学
细胞生物学
癌症研究
医学
转录因子
基因
环境卫生
作者
Amelie Köhler,Anna-Lena Geiselhöringer,Daphne Kolland,Luisa Kreft,Nina O. Wichmann,Miriam Hils,Mária Pásztói,Elena Zurkowski,Johannes F. Vogt,Tanja Kübelbeck,Tilo Biedermann,Ingo Schmitz,Wiebke Hansen,Daniela Kramer,Matthias M. Gaida,Carsten B. Schmidt‐Weber,Nadine Hoevelmeyer,Caspar Ohnmacht
标识
DOI:10.1016/j.mucimm.2024.04.002
摘要
Peripherally-induced regulatory T cells (pTregs) expressing the retinoic acid receptor-related orphan-receptor gamma t (RORγt) are indispensable for intestinal immune homeostasis. Nuclear factor kappa family members regulate the differentiation of thymic Tregs and promote their survival in the periphery. However, the Treg intrinsic molecular mechanisms controlling the size of the pTregs in the intestine and associated lymphoid organs remain unclear. Here, we provide direct evidence that B-cell lymphoma 3 (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
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