SATB1 dictates expression of multiple genes including IL-5 involved in human T helper cell differentiation

被引:57
作者
Ahlfors, Helena [1 ,2 ,3 ]
Limaye, Amita [4 ]
Elo, Laura L. [1 ,2 ,5 ]
Tuomela, Soile [1 ,2 ,6 ]
Burute, Mithila [4 ]
Gottimukkala, Kamal Vishnu P. [4 ]
Notani, Dimple [4 ]
Rasool, Omid [1 ,2 ]
Galande, Sanjeev [4 ,7 ]
Lahesmaa, Riitta [1 ,2 ]
机构
[1] Univ Turku, Turku Ctr Biotechnol, FIN-20521 Turku, Finland
[2] Abo Akad Univ, Turku, Finland
[3] Natl Grad Sch Informat & Struct Biol, Turku, Finland
[4] Natl Ctr Cell Sci, Pune, Maharashtra, India
[5] Univ Turku, Dept Math, SF-20500 Turku, Finland
[6] Turku Grad Sch Biomed Sci, Turku, Finland
[7] Indian Inst Sci Educ & Res, Pune 411021, Maharashtra, India
基金
英国惠康基金; 芬兰科学院;
关键词
COORDINATED EXPRESSION; BINDING-SITES; IDENTIFICATION; TRANSCRIPTION; STAT6; CHROMATIN; LINEAGE; BIOCONDUCTOR; INFLAMMATION; ARCHITECTURE;
D O I
10.1182/blood-2009-11-252205
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Special AT-rich binding protein 1 (SATB1) is a global chromatin organizer and a transcription factor regulated by interleukin-4 (IL-4) during the early T helper 2 (Th2) cell differentiation. Here we show that SATB1 controls multiple IL-4 target genes involved in human Th cell polarization or function. Among the genes regulated by SATB1 is that encoding the cytokine IL-5, which is predominantly produced by Th2 cells and plays a key role in the development of eosinophilia in asthma. We demonstrate that, during the early Th2 cell differentiation, IL-5 expression is repressed through direct binding of SATB1 to the IL-5 promoter. Furthermore, SATB1 knockdown-induced upregulation of IL-5 is partly counteracted by down-regulating GATA3 expression using RNAi in polarizing Th2 cells. Our results suggest that a competitive mechanism involving SATB1 and GATA3 regulates IL-5 transcription, and provide new mechanistic insights into the stringent regulation of IL-5 expression during human Th2 cell differentiation. (Blood. 2010;116(9):1443-1453)
引用
收藏
页码:1443 / 1453
页数:11
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