Insights into transcriptional regulation by FOXP3

被引:13
作者
Carson, BD
Lopes, JE
Soper, DM
Ziegler, SF
机构
[1] Benaroya Res Inst, Seattle, WA 98101 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
fox; FoxP3; FoxD1; FoxD2; FoxN1; FoxJ1; FoxO; FoxO3a; FoxO1; FoxQ1; treg; T-reg; regulatory T cell; transcription factor; microarray; IPEX; scurfy; SLE; autoimmunity; tolerance; CTLA-4; GITR; TNFRSF18; TGF-beta; LAG-3; SOCS2; TIAM-1; GBP-3; CD25; CD122; IL-2R-beta; interleukin-2 receptor beta chain; OX40; TNFRSF4; NRP-1; neuropilin-1; CD81; TAPA-1; lymphotoxin; ECM-1; OCTN-2; SLC22A5; beta-enolase; NF-AT; NF-kappaB; NF-kB; glutamine-rich; polyglutamine; forkhead; winged-helix; zinc finger; C2H2; leucine zipper; review;
D O I
10.2741/1908
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
FoxP3 recently entered the spotlight as a critical component of regulatory T cell development and function. Several groups are presently engaged in an effort to uncover the mechanistic details of its contribution to this critical T cell subset. Despite this, the mechanism of FoxP3-mediated transcriptional repression and the affected target genes are still largely unknown. First, we discuss insights from work on other Fox family members with an emphasis on those with known roles in the immune system. Second, we review recent data concerning the molecular mechanism of FoxP3 function and its role in human disease. Finally, we consider what is known about FoxP3 target genes and their effect on T cell physiology.
引用
收藏
页码:1607 / 1619
页数:13
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