p21ras and calcineurin synergize to regulate the nuclear factor of activated T cells

M. Woodrow, Neil A. Clipstone, D. Cantrell

Research output: Contribution to journalArticle

120 Citations (Scopus)

Abstract

In T lymphocytes, triggering of the T cell receptor (TCR) induces several signaling cascades which ultimately synergize to induce the activity of the nuclear factor of activated T cells (NFAT), a DNA binding complex critical to the inducibility and T cell specificity of the T cell growth factor interleukin 2. One immediate consequence of T cell activation via the TCR is an increase in cytosolic calcium. Calcium signals are important for NFAT induction, and recent studies have identified calcineurin, a calcium-calmodulin dependent serine-threonine phosphatase, as a prominent component of the calcium signaling pathway in T ceils. A second important molecule in TCR signal transduction is the guanine nucleotide binding protein, p21ras, which is coupled to the TCR by a protein tyrosine kinase dependent mechanism. The experiments presented here show that expression by transfection of mutationally activated calcineurin or activated p21ras alone is insuffident for NFAT transactivation. However, coexpression of the activated calcineurin with activated p21ras could mimic TCR signals in NFAT induction. These data identify calcineurin and p21ras as cooperative partners in T cell activation.

Original languageEnglish
Pages (from-to)1517-1522
Number of pages6
JournalJournal of Experimental Medicine
Volume178
Issue number5
DOIs
Publication statusPublished - 1 Nov 1993

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