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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/25904
Title: Inhibiting the calcineurin-NFAT (nuclear factor of activated T cells) signaling pathway with a regulator of calcineurin-derived peptide without affecting general calcineurin phosphatase activity
Authors: Mulero, M. Carmen; Aubareda, Anna; Orzáez, Mar; Messeguer, Joaquim; Serrano-Candelas, Eva; Martínez-Hoyer, Sergio; Messeguer Peypoch, Ángel; Pérez-Payá, Enrique ; Pérez-Riba, Mercè
Issue Date: 3-Apr-2009
Publisher: American Society for Biochemistry and Molecular Biology
Citation: Journal of Biological Chemistry 284(14): 9394-9401 (2009)
Abstract: Calcineurin phosphatase plays a crucial role in T cell activation. Dephosphorylation of the nuclear factors of activated T cells (NFATs) by calcineurin is essential for activating cytokine gene expression and, consequently, the immune response. Current immunosuppressive protocols are based mainly on calcineurin inhibitors, cyclosporine A and FK506. Unfortunately, these drugs are associated with severe side effects. Therefore, immunosuppressive agents with higher selectivity and lower toxicity must be identified. The immunosuppressive role of the family of proteins regulators of calcineurin (RCAN, formerly known as DSCR1) which regulate the calcineurin-NFAT signaling pathway, has been described recently. Here, we identify and characterize the minimal RCAN sequence responsible for the inhibition of calcineurin-NFAT signaling in vivo. The RCAN-derived peptide spanning this sequence binds to calcineurin with high affinity. This interaction is competed by a peptide spanning the NFAT PXIXIT sequence, which binds to calcineurin and facilitates NFAT dephosphorylation and activation. Interestingly, the RCAN-derived peptide does not inhibit general calcineurin phosphatase activity, which suggests that it may have a specific immunosuppressive effect on the calcineurin-NFAT signaling pathway. As such, the RCAN-derived peptide could either be considered a highly selective immunosuppressive compound by itself or be used as a new tool for identifying innovative immunosuppressive agents. We developed a low throughput assay, based on the RCAN1-calcineurin interaction, which identifies dipyridamole as an efficient in vivo inhibitor of the calcineurin-NFAT pathway that does not affect calcineurin phosphatase activity.
Description: 8 pages, 5 figures.-- PMID: 19189965 [PubMed].-- PMCID: PMC2666591.-- Supplementary information available at: http://www.jbc.org/content/suppl/2009/02/05/M805889200.DC1.html
Publisher version (URL): http://dx.doi.org/10.1074/jbc.M805889200
URI: http://hdl.handle.net/10261/25904
DOI: 10.1074/jbc.M805889200
ISSN: 0021-9258 (Print)
1083-351X (Online)
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