Ziegler Liesa S, Gerner Marlene C, Schmidt Ralf L J, Trapin Doris, Steinberger Peter, Pickl Winfried F, Sillaber Christian, Egger Gerda, Schwarzinger Ilse, Schmetterer Klaus G
Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Institute of Immunology, Medical University of Vienna, Vienna, Austria.
FEBS J. 2021 Jan;288(2):640-662. doi: 10.1111/febs.15361. Epub 2020 May 28.
Nuclear factor 'κ-light-chain-enhancer' of activated B cells (NF-κB) signaling is a signaling pathway used by most immune cells to promote immunostimulatory functions. Recent studies have indicated that regulatory T cells (Treg) differentially integrate TCR-derived signals, thereby maintaining their suppressive features. However, the role of NF-κB signaling in the activation of human peripheral blood (PB) Treg has not been fully elucidated so far. We show that the activity of the master transcription factor forkhead box protein 3 (FOXP3) attenuates p65 phosphorylation and nuclear translocation of the NF-κB proteins p50, p65, and c-Rel following activation in human Treg. Using pharmacological and genetic inhibition of canonical NF-κB signaling in FOXP3-transgenic T cells and PB Treg from healthy donors as well as Treg from a patient with a primary NFKB1 haploinsufficiency, we validate that Treg activation and suppressive capacity is independent of NF-κB signaling. Additionally, repression of residual NF-κB signaling in Treg further enhances interleukin-10 (IL-10) production. Blockade of NF-κB signaling can be exploited for the generation of in vitro induced Treg (iTreg) with enhanced suppressive capacity and functional stability. In this respect, dual blockade of mammalian target of rapamycin (mTOR) and NF-κB signaling was accompanied by enhanced expression of the transcription factors FOXP1 and FOXP3 and demethylation of the Treg-specific demethylated region compared to iTreg generated under mTOR blockade alone. Thus, we provide first insights into the role of NF-κB signaling in human Treg. These findings could lead to strategies for the selective manipulation of Treg and the generation of improved iTreg for cellular therapy.
活化B细胞的核因子“κ轻链增强子”(NF-κB)信号传导是大多数免疫细胞用于促进免疫刺激功能的信号通路。最近的研究表明,调节性T细胞(Treg)以不同方式整合TCR衍生信号,从而维持其抑制特性。然而,迄今为止,NF-κB信号传导在人外周血(PB)Treg激活中的作用尚未完全阐明。我们发现,在人Treg激活后,主转录因子叉头框蛋白3(FOXP3)的活性会减弱NF-κB蛋白p50、p65和c-Rel的p65磷酸化及核转位。通过对FOXP3转基因T细胞、健康供体的PB Treg以及一名原发性NFKB1单倍体不足患者的Treg中经典NF-κB信号传导进行药理学和基因抑制,我们证实Treg的激活和抑制能力独立于NF-κB信号传导。此外,抑制Treg中残余的NF-κB信号传导可进一步增强白细胞介素10(IL-10)的产生。阻断NF-κB信号传导可用于生成具有增强抑制能力和功能稳定性的体外诱导Treg(iTreg)。在这方面,与单独在mTOR阻断下生成的iTreg相比,雷帕霉素靶蛋白(mTOR)和NF-κB信号传导的双重阻断伴随着转录因子FOXP1和FOXP3表达的增强以及Treg特异性去甲基化区域的去甲基化。因此,我们首次深入了解了NF-κB信号传导在人Treg中的作用。这些发现可能会带来选择性操纵Treg的策略以及生成用于细胞治疗的改良iTreg的方法。