Transcription factor KLF2 regulates the migration of naive T cells by restricting chemokine receptor expression patterns

被引:152
作者
Sebzda, Eric [1 ]
Zou, Zhiying [1 ]
Lee, John S. [1 ]
Wang, Tao [1 ]
Kahn, Mark L. [1 ]
机构
[1] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
关键词
D O I
10.1038/ni1565
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The migration patterns of naive and activated T cells are associated with the expression of distinct sets of chemokine receptors, but the molecular basis for this regulation is unknown. Here we identify Krupple-like factor 2 (KLF2) as a key transcriptional factor needed to prevent naive T cells from expressing inflammatory chemokine receptors and acquiring the migration patterns of activated T cells. Lineage-specific deletion of KLF2 resulted in fewer naive T cells in the blood and secondary lymphoid organs, whereas it expanded naive T cell numbers in nonlymphoid tissues; these effects were associated with altered expression of inflammatory chemokine receptors on naive T cells. KLF2 repressed the expression of several chemokine receptors, including CCR3 and CCR5. We thus conclude that KLF2 maintains proper T cell migration patterns by linking T cell movement and transcriptional regulation of chemokine receptor expression patterns.
引用
收藏
页码:292 / 300
页数:9
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