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USP21 可阻止 T 辅助 1 样调节性 T 细胞的产生。

USP21 prevents the generation of T-helper-1-like Treg cells.

机构信息

Key Laboratory of Molecular Virology and Immunology, CAS Center for Excellence in Molecular Cell Science, Unit of Molecular Immunology, Institut Pasteur of Shanghai, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200025, China.

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

Nat Commun. 2016 Nov 18;7:13559. doi: 10.1038/ncomms13559.

Abstract

FOXP3 Regulatory T (Treg) cells play a key role in the maintenance of immune homeostasis and tolerance. Disruption of Foxp3 expression results in the generation of instable Treg cells and acquisition of effector T-cell-like function. Here we report that the E3 deubiquitinase USP21 prevents the depletion of FOXP3 at the protein level and restricts the generation of T-helper-1-like Treg cells. Mice depleted of Usp21 specifically in Treg cells display immune disorders characterized by spontaneous T-cell activation and excessive T-helper type 1 (Th1) skewing of Treg cells into Th1-like Treg cells. USP21 stabilizes FOXP3 protein by mediating its deubiquitination and maintains the expression of Treg signature genes. Our results demonstrate how USP21 prevents FOXP3 protein depletion and controls Treg lineage stability in vivo.

摘要

叉头框蛋白 3(FOXP3)调节性 T(Treg)细胞在维持免疫稳态和耐受中发挥关键作用。Foxp3 表达的破坏会导致不稳定的 Treg 细胞的产生,并获得效应 T 细胞样功能。在这里,我们报告 E3 去泛素化酶 USP21 可防止 FOXP3 在蛋白质水平上的耗竭,并限制辅助性 T 细胞 1 样 Treg 细胞的生成。在 Treg 细胞中特异性缺失 Usp21 的小鼠表现出免疫紊乱的特征,表现为自发的 T 细胞激活和 Treg 细胞向 Th1 样 Treg 细胞的过度 Th1 偏斜。USP21 通过介导其去泛素化稳定 FOXP3 蛋白,并维持 Treg 特征基因的表达。我们的结果表明了 USP21 如何防止 FOXP3 蛋白耗竭并控制体内 Treg 谱系稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef02/5120220/34b6d4aa92ee/ncomms13559-f1.jpg

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