Unknown

Dataset Information

0

Lkb1 maintains Treg cell lineage identity.


ABSTRACT: Regulatory T (Treg) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve Treg lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains Treg cell lineage identity by stabilizing Foxp3 expression and enforcing suppressor function. Upon T-cell receptor (TCR) stimulation Lkb1 protein expression is upregulated in Treg cells but not in conventional T cells. Mice with Treg cell-specific deletion of Lkb1 develop a fatal early-onset autoimmune disease, with no Foxp3 expression in most Treg 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-? signalling. These findings identify a critical function of Lkb1 in maintaining Treg cell lineage identity.

SUBMITTER: Wu D 

PROVIDER: S-EPMC5481770 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications


Regulatory T (T<sub>reg</sub>) cells are a distinct T-cell lineage characterized by sustained Foxp3 expression and potent suppressor function, but the upstream dominant factors that preserve T<sub>reg</sub> lineage-specific features are mostly unknown. Here, we show that Lkb1 maintains T<sub>reg</sub> cell lineage identity by stabilizing Foxp3 expression and enforcing suppressor function. Upon T-cell receptor (TCR) stimulation Lkb1 protein expression is upregulated in T<sub>reg</sub> cells but n  ...[more]

Similar Datasets

| S-EPMC5804356 | biostudies-literature
| S-EPMC4700479 | biostudies-literature
| S-EPMC3037591 | biostudies-literature
| S-EPMC4377859 | biostudies-literature
| S-EPMC6685710 | biostudies-literature
| S-EPMC3950964 | biostudies-literature
2023-02-04 | GSE203536 | GEO
2023-02-21 | GSE203492 | GEO
2023-02-20 | GSE203606 | GEO
| S-EPMC9908423 | biostudies-literature