FoxP3, Helios, and SATB1: Roles and relationships in regulatory T cells

被引:32
作者
Grzanka, Jakub [1 ]
Leveson-Gower, Dennis [1 ]
Golab, Karolina [1 ]
Wang, Xiao-Jun [1 ]
Marek-Trzonkowska, Natalia [2 ]
Krzystyniak, Adam [2 ]
Wardowska, Anna [2 ]
Mills, J. Michael [1 ]
Trzonkowski, Piotr [2 ]
Witkowski, Piotr [1 ]
机构
[1] Univ Chicago, Dept Surg, Sect Transplantat, Chicago, IL 60637 USA
[2] Med Univ Gdansk, Dept Clin Immunol & Transplantol, Gdansk, Poland
关键词
FoxP3; Helios; SATB1; Immunotherapy; T regulatory cells; Treg; TRANSCRIPTION FACTOR FOXP3; IMMUNOLOGICAL SELF-TOLERANCE; TUMOR-BEARING HOSTS; TGF-BETA; EXPRESSION; RECEPTOR; INTERLEUKIN-2; IL-2; PROTEIN; DIFFERENTIATION;
D O I
10.1016/j.intimp.2013.02.004
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 (Treg) play pivotal role in the maintenance of immune homeostasis due to their suppressive abilities. It is important to understand the nature of Treg and the mechanisms by which they function. From recent studies, we can conclude that the development and function of Treg cells is strongly dependent on gene expression. Furthermore, a variety of transcription factors have been proposed to either maintain or inhibit their properties. As it was demonstrated a decade ago, Forkhead box P3 transcription factor (FoxP3), a Treg marker, has the ability to keep them on the right immunosuppressive track. Whether the Treg lineage has the ability of being suppressive or not depends on up- or down-regulation of the foxp3 gene. It can be controlled by other factors present inside the cell. Two of them, Helios and SATB1, are considered to be important in proper Treg development. Helios, a member of the Ikaros family, has been shown to up-regulate expression of FoxP3 protein, whereas SATB1 is known to inhibit its expression. In this review, we will discuss the relations between these three factors, and how they affect Treg development and function. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 347
页数:5
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