Tcf1 and Lef1 are required for the immunosuppressive function of regulatory T cells.
Shaojun XingKexin GaiXiang LiPeng ShaoZhouhao ZengXudong ZhaoXin ZhaoXia ChenWilliam J ParadeeDavid K MeyerholzWeiqun PengHai-Hui XuePublished in: The Journal of experimental medicine (2019)
Tcf1 and Lef1 have versatile functions in regulating T cell development and differentiation, but intrinsic requirements for these factors in regulatory T (T reg) cells remain to be unequivocally defined. Specific ablation of Tcf1 and Lef1 in T reg cells resulted in spontaneous multi-organ autoimmunity that became more evident with age. Tcf1/Lef1-deficient T regs showed reduced protection against experimentally induced colitis, indicative of diminished immuno-suppressive capacity. Transcriptomic analysis revealed that Tcf1 and Lef1 were responsible for positive regulation of a subset of T reg-overrepresented signature genes such as Ikzf4 and Izumo1r Unexpectedly, Tcf1 and Lef1 were necessary for restraining expression of cytotoxic CD8+ effector T cell-associated genes in T reg cells, including Prdm1 and Ifng Tcf1 ChIP-seq revealed substantial overlap between Tcf1 and Foxp3 binding peaks in the T reg cell genome, with Tcf1-Foxp3 cooccupancy observed at key T reg signature and cytotoxic effector genes. Our data collectively indicate that Tcf1 and Lef1 are critical for sustaining T reg suppressive functions and preventing loss of self-tolerance.
Keyphrases
- regulatory t cells
- induced apoptosis
- genome wide
- dendritic cells
- single cell
- cell cycle arrest
- poor prognosis
- gene expression
- acute lymphoblastic leukemia
- oxidative stress
- mesenchymal stem cells
- machine learning
- binding protein
- cell death
- big data
- electronic health record
- pi k akt
- rna seq
- dna binding
- radiofrequency ablation
- nk cells
- high throughput sequencing