FoxP3 in Treg cell biology: a molecular and structural perspective

被引:36
|
作者
Deng, G. [1 ]
Song, X. [2 ]
Greene, M. I. [3 ]
机构
[1] Peking Univ, Sch Basic Med Sciences, Dept Immunol, Beijing, Beijing, Peoples R China
[2] Chinese Acad Sciences, Inst Biochem,CAS Ctr Excellence Mol Cell Sci, State Key Lab Mol Biol,Cell Biol, Shanghai, Shanghai, Peoples R China
[3] Univ Penn, Perelman Sch Med, Dept Pathol, Lab Med, Philadelphia, PA USA
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 2020年 / 199卷 / 03期
关键词
allosteric modifiers; FoxP3; protein interactions; post-translational modifications; regulatory T cells; TRANSCRIPTION FACTOR FOXP3; TARGET GENES; PROTEIN; STABILITY; DOMAIN; ALPHA; DIFFERENTIATION; TRANSPLANTATION; AUTOIMMUNITY; DEACETYLASES;
D O I
10.1111/cei.13357
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (T-regs) are specialized in immune suppression and play a dominant role in peripheral immune tolerance. T-reg cell lineage development and function maintenance is determined by the forkhead box protein 3 (FoxP3) transcriptional factor, whose activity is fine-tuned by its post-translational modifications (PTMs) and interaction partners. In this review, we summarize current studies in the crystal structures, the PTMs and interaction partners of FoxP3 protein, and discuss how these insights may provide a roadmap for new approaches to modulate T-reg suppression, and new therapies to enhance immune tolerance in autoimmune diseases.
引用
收藏
页码:255 / 262
页数:8
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