Proteins of the nuclear factor of activated T cells (NFAT) family of transcription factors are critical for lymphocyte activation in the immune system. In particular, NFATs are important regulators of inducible IL-4 gene expression. Interferon regulatory factor 4 (IRF4) is an immune system–restricted interferon regulatory factor that is required for lymphocyte activation, but its molecular functions in the T lineage remain to be elucidated. We demonstrate that IRF4 potently synergizes with NFATc2 to specifically enhance NFATc2-driven transcriptional activation of the IL-4 promoter. This function is dependent on the physical interaction of IRF4 with NFATc2. IRF4 synergizes with NFATc2 and the IL-4–inducing transcription factor, c-maf, to augment IL-4 promoter activity as well as to elicit significant levels of endogenous IL-4 production. Furthermore, naïve T helper cells from mice lacking IRF4 are compromised severely for the production of IL-4 and other Th2 cytokines. The identification of IRF4 as a partner for NFATc2 in IL-4 gene regulation provides an important molecular function for IRF4 in T helper cell differentiation.
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15 April 2002
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April 08 2002
Interferon Regulatory Factor 4 (IRF4) Interacts with NFATc2 to Modulate Interleukin 4 Gene Expression
Jyothi Rengarajan,
Jyothi Rengarajan
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
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Kerri A. Mowen,
Kerri A. Mowen
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
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Kathryn D. McBride,
Kathryn D. McBride
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
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Erica D. Smith,
Erica D. Smith
3Howard Hughes Medical Institute, The University of Chicago, Chicago, IL 60637
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Harinder Singh,
Harinder Singh
3Howard Hughes Medical Institute, The University of Chicago, Chicago, IL 60637
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Laurie H. Glimcher
Laurie H. Glimcher
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
2Department of Medicine, Harvard Medical School, Boston, MA 02115
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Jyothi Rengarajan
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
Kerri A. Mowen
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
Kathryn D. McBride
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
Erica D. Smith
3Howard Hughes Medical Institute, The University of Chicago, Chicago, IL 60637
Harinder Singh
3Howard Hughes Medical Institute, The University of Chicago, Chicago, IL 60637
Laurie H. Glimcher
1Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, MA 02115
2Department of Medicine, Harvard Medical School, Boston, MA 02115
Address correspondence to L.H. Glimcher, Department of Immunology and Infectious Disease, Harvard School of Public Health, Harvard Medical School, Boston, MA 02115. Phone: (617) 432-0622; Fax: (617) 432-0084; E-mail: [email protected]
*
Abbreviations used in this paper: CsA, cyclosporin A; HA, hemagglutinin; HRP, horseradish peroxidase; IRF4, interferon regulatory factor 4; NFAT, nuclear factor of activated T cells; NIP45, NFAT-interacting protein 45.
Received:
June 28 2001
Revision Received:
February 15 2002
Accepted:
March 01 2002
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2002
J Exp Med (2002) 195 (8): 1003–1012.
Article history
Received:
June 28 2001
Revision Received:
February 15 2002
Accepted:
March 01 2002
Citation
Jyothi Rengarajan, Kerri A. Mowen, Kathryn D. McBride, Erica D. Smith, Harinder Singh, Laurie H. Glimcher; Interferon Regulatory Factor 4 (IRF4) Interacts with NFATc2 to Modulate Interleukin 4 Gene Expression . J Exp Med 15 April 2002; 195 (8): 1003–1012. doi: https://doi.org/10.1084/jem.20011128
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