Control of the Inheritance of Regulatory T Cell Identity by a cis Element in the Foxp3 Locus

被引:387
作者
Feng, Yongqiang
Arvey, Aaron
Chinen, Takatoshi
van der Veeken, Joris
Gasteiger, Georg
Rudensky, Alexander Y. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Ludwig Ctr, Howard Hughes Med Inst, New York, NY 10065 USA
关键词
IN-VIVO; EXPRESSION; INDUCTION; GENE; DIFFERENTIATION; PLASTICITY; LINEAGE; DEMETHYLATION; STIMULATION; ACTIVATION;
D O I
10.1016/j.cell.2014.07.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In multicellular organisms, specialized functions are delegated to distinct cell types whose identity and functional integrity are maintained upon challenge. However, little is known about the mechanisms enabling lineage inheritance and their biological implications. Regulatory T (Treg) cells, which express the transcription factor Foxp3, suppress fatal auto-immunity throughout the lifespan of animals. Here, we show that a dedicated Foxp3 intronic element CNS2 maintains Treg cell lineage identity by acting as a sensor of the essential Treg cell growth factor IL-2 and its downstream target STAT5. CNS2 sustains Foxp3 expression during division of mature Treg cells when IL-2 is limiting and counteracts proinflammatory cytokine signaling that leads to the loss of Foxp3. CNS2-mediated stable inheritance of Foxp3 expression is critical for adequate suppression of diverse types of chronic inflammation by Treg cells and prevents their differentiation into inflammatory effector cells. The described mechanism may represent a general principle of the inheritance of differentiated cell states.
引用
收藏
页码:749 / 763
页数:15
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