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Lkb1 maintains T(reg) cell lineage identity
Regulatory T (T(reg)) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T(reg) lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T(reg) cell lineage identity by...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481770/ https://www.ncbi.nlm.nih.gov/pubmed/28621313 http://dx.doi.org/10.1038/ncomms15876 |
Sumario: | Regulatory T (T(reg)) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T(reg) lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T(reg) cell lineage identity by stabilizing Foxp3 expression and enforcing suppressor function. Upon T-cell receptor (TCR) stimulation Lkb1 protein expression is upregulated in T(reg) cells but not in conventional T cells. Mice with T(reg) cell-specific deletion of Lkb1 develop a fatal early-onset autoimmune disease, with no Foxp3 expression in most T(reg) cells. Lkb1 stabilizes Foxp3 expression by preventing STAT4-mediated methylation of the conserved noncoding sequence 2 (CNS2) in the Foxp3 locus. Independent of maintaining Foxp3 expression, Lkb1 programs the expression of a wide spectrum of immunosuppressive genes, through mechanisms involving the augmentation of TGF-β signalling. These findings identify a critical function of Lkb1 in maintaining T(reg) cell lineage identity. |
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