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The ubiquitin ligase Peli1 negatively regulates T cell activation and prevents autoimmunity.


ABSTRACT: T cell activation is subject to tight regulation to avoid inappropriate responses to self antigens. Here we show that genetic deficiency in the ubiquitin ligase Peli1 caused hyperactivation of T cells and rendered T cells refractory to suppression by regulatory T cells and transforming growth factor-? (TGF-?). As a result, Peli1-deficient mice spontaneously developed autoimmunity characterized by multiorgan inflammation and autoantibody production. Peli1 deficiency resulted in the nuclear accumulation of c-Rel, a member of the NF-?B family of transcription factors with pivotal roles in T cell activation. Peli1 negatively regulated c-Rel by mediating its Lys48 (K48) ubiquitination. Our results identify Peli1 as a critical factor in the maintenance of peripheral T cell tolerance and demonstrate a previously unknown mechanism of c-Rel regulation.

SUBMITTER: Chang M 

PROVIDER: S-EPMC3178748 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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The ubiquitin ligase Peli1 negatively regulates T cell activation and prevents autoimmunity.

Chang Mikyoung M   Jin Wei W   Chang Jae-Hoon JH   Xiao Yichuan Y   Brittain George C GC   Yu Jiayi J   Zhou Xiaofei X   Wang Yi-Hong YH   Cheng Xuhong X   Li Pingwei P   Rabinovich Brian A BA   Hwu Patrick P   Sun Shao-Cong SC  

Nature immunology 20110828 10


T cell activation is subject to tight regulation to avoid inappropriate responses to self antigens. Here we show that genetic deficiency in the ubiquitin ligase Peli1 caused hyperactivation of T cells and rendered T cells refractory to suppression by regulatory T cells and transforming growth factor-β (TGF-β). As a result, Peli1-deficient mice spontaneously developed autoimmunity characterized by multiorgan inflammation and autoantibody production. Peli1 deficiency resulted in the nuclear accumu  ...[more]

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