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

Author:

Ahlfors Helena12,Limaye Amita3,Elo Laura L.14,Tuomela Soile15,Burute Mithila3,Gottimukkala Kamal Vishnu P.3,Notani Dimple3,Rasool Omid1,Galande Sanjeev36,Lahesmaa Riitta1

Affiliation:

1. Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, Finland;

2. National Graduate School in Informational and Structural Biology, Turku, Finland;

3. National Centre for Cell Science, Ganeshkhind, Pune, India;

4. Department of Mathematics, University of Turku, Turku, Finland;

5. Turku Graduate School for Biomedical Sciences, Turku, Finland; and

6. Indian Institute of Science Education and Research, Pashan, Pune, India

Abstract

Abstract 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 up-regulation 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.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference51 articles.

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