4.6 Article

TOX Is Required for Development of the CD4 T Cell Lineage Gene Program

期刊

JOURNAL OF IMMUNOLOGY
卷 187, 期 11, 页码 5931-5940

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1101474

关键词

-

资金

  1. National Institutes of Health [R01AI054977]

向作者/读者索取更多资源

The factors that regulate thymic development of the CD4(+) T cell gene program remain poorly defined. The transcriptional regulator ThPOK is a dominant factor in CD4(+) T cell development, which functions primarily to repress the CD8 lineage fate. Previously, we showed that nuclear protein TOX is also required for murine CD4(+) T cell development. In this study, we sought to investigate whether the requirement for TOX was solely due to a role in ThPOK induction. In apparent support of this proposition, ThPOK upregulation and CD8 lineage repression were compromised in the absence of TOX, and enforced ThPOK expression could restore some CD4 development. However, these rescued CD4 cells were defective in many aspects of the CD4(+) T cell gene program, including expression of Id2, Foxol, and endogenous Thpok, among others. Thus, TOX is necessary to establish the CD4(+) T cell lineage gene program, independent of its influence on ThPOK expression. The Journal of Immunology, 2011, 187: 5931-5940.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据