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Th2细胞分化及Il4基因座可及性的调控

Regulation of Th2 differentiation and Il4 locus accessibility.

作者信息

Ansel K Mark, Djuretic Ivana, Tanasa Bogdan, Rao Anjana

机构信息

Harvard Medical School, CBR Institute for Biomedical Research, Boston, Massachusetts 02115, USA.

出版信息

Annu Rev Immunol. 2006;24:607-56. doi: 10.1146/annurev.immunol.23.021704.115821.

Abstract

Helper T cells coordinate immune responses through the production of cytokines. Th2 cells express the closely linked Il4, Il13, and Il5 cytokine genes, whereas these same genes are silenced in the Th1 lineage. The Th1/Th2 lineage choice has become a textbook example for the regulation of cell differentiation, and recent discoveries have further refined and expanded our understanding of how Th2 differentiation is initiated and reinforced by signals from antigen-presenting cells and cytokine-driven feedback loops. Epigenetic changes that stabilize the active or silent state of the Il4 locus in differentiating helper T cells have been a major focus of recent research. Overall, the field is progressing toward an integrated model of the signaling and transcription factor networks, cis-regulatory elements, epigenetic modifications, and RNA interference mechanisms that converge to determine the lineage fate and gene expression patterns of differentiating helper T cells.

摘要

辅助性T细胞通过产生细胞因子来协调免疫反应。Th2细胞表达紧密连锁的Il4、Il13和Il5细胞因子基因,而这些相同的基因在Th1谱系中是沉默的。Th1/Th2谱系选择已成为细胞分化调控的一个教科书式例子,最近的发现进一步完善和扩展了我们对Th2分化如何由抗原呈递细胞的信号和细胞因子驱动的反馈回路启动和加强的理解。稳定分化中的辅助性T细胞中Il4基因座的活性或沉默状态的表观遗传变化一直是最近研究的主要焦点。总体而言,该领域正在朝着信号和转录因子网络、顺式调控元件、表观遗传修饰和RNA干扰机制的整合模型发展,这些机制共同作用以决定分化中的辅助性T细胞的谱系命运和基因表达模式。

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