Calcium-Dependent Activation of TNF Family Gene Expression by Ca2+/Calmodulin Kinase Type IV/Gr and Calcineurin

Author:

Lobo Francis M.1,Zanjani Reza2,Ho Nga3,Chatila Talal A.3,Fuleihan Ramsay L.2

Affiliation:

1. †Internal Medicine, Yale University School of Medicine, New Haven, CT 06520; and

2. *Yale Child Health Research Center and Sections of Immunology, Department of Pediatrics, and

3. ‡Division of Immunology and Rheumatology, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110

Abstract

Abstract CD40 ligand (L), FasL, and TNF-α are members of the TNF family of cytokines. All are expressed by T lymphocytes shortly after activation but have distinct effector functions. Transcription of these genes can be induced by stimulation of T cells by calcium ionophore alone and requires the calcineurin-dependent transcription factor NF of activated T cells. We have examined a second calcium-dependent signaling pathway, mediated by calcium/calmodulin-dependent kinase IV (CaMKIV) in transcriptional activation of TNF family genes. In reporter gene assays using constructs driven by the promoters of human CD40L, FasL, or TNF-α along with vectors expressing constitutively active CaMKIV and calcineurin, we have demonstrated that each promoter is activated by calcineurin and CaMKIV in a synergistic fashion. Furthermore, specific inhibition of CaMKIV by chemical means and by a dominant negative mutant of CaMKIV impairs the ionomycin-induced activity of all three promoters as well as protein expression of CD40L and TNF-α. Our results indicate that activation of gene expression by calcineurin and CaMKIV is common to members of the TNF cytokine family.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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