Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Curr Top Microbiol Immunol. 2012;356:165-88. doi: 10.1007/82_2011_175.
Developing αβ T cells choose between the helper and cytotoxic lineages, depending upon the specificity of their T cell receptors for MHC molecules. The expression of the CD4 co-receptor on helper cells and the CD8 co-receptor on cytotoxic cells is intimately linked to this decision, and their regulation at the transcriptional level has been the subject of intense study to better understand lineage choice. Indeed, as the fate of developing T cells is decided, the expression status of these genes is accordingly locked. Genetic models have revealed important transcriptional elements and the ability to manipulate these elements in the framework of development has added a new perspective on the temporal nature of their function and the epigenetic maintenance of gene expression. We examine here novel insights into epigenetic mechanisms that have arisen through the study of these genes.
αβ T 细胞的发育会根据其 T 细胞受体对 MHC 分子的特异性,在辅助性和细胞毒性谱系之间做出选择。辅助性细胞上 CD4 共受体的表达和细胞毒性细胞上 CD8 共受体的表达与这一决定密切相关,其在转录水平的调控一直是深入研究以更好地理解谱系选择的主题。事实上,随着发育中 T 细胞命运的决定,这些基因的表达状态被锁定。遗传模型揭示了重要的转录元件,并且在发育框架中操纵这些元件的能力为其功能的时间性质和基因表达的表观遗传维持提供了新的视角。我们在这里研究了通过研究这些基因而产生的表观遗传机制的新见解。