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Molecular and Cellular Biology, March 2006, p. 2327-2336, Vol. 26, No. 6
0270-7306/06/$08.00+0 doi:10.1128/MCB.26.6.2327-2336.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
CARMA1 Is Required for Akt-Mediated NF-
B Activation in T Cells
Preeti Narayan,
Brittany Holt,
Richard Tosti, and
Lawrence P. Kane*
Department of Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania 15261
Received 19 October 2005/
Returned for modification 15 November 2005/
Accepted 23 December 2005
Many details of the generic pathway for induction of NF-
B have been delineated, but it is still not clear how multiple, diverse receptor systems are able to converge on this evolutionarily conserved family of transcription factors. Recent studies have shown that the CARMA1, Bcl10, and MALT1 proteins are critical for coupling the common elements of the NF-
B pathway to the T-cell receptor (TCR) and CD28. We previously demonstrated a role for the serine/threonine kinase Akt in CD28-mediated NF-
B induction. Using a CARMA1-deficient T-cell line, we have now found that the CARMA complex is required for induction of NF-
B by Akt, in cooperation with protein kinase C activation. Furthermore, using a novel selective inhibitor of Akt, we confirm that Akt plays a modulatory role in NF-
B induction by the TCR and CD28. Finally, we provide evidence for a physical and functional interaction between Akt and CARMA and for Akt-dependent phosphorylation of Bcl10. Therefore, in T cells, Akt impinges upon NF-
B signaling through at least two separate mechanisms.
* Corresponding author. Mailing address: Department of Immunology, BST E-1056, University of Pittsburgh School of Medicine, 200 Lothrop St., Pittsburgh, PA 15261. Phone: (412) 648-8947. Fax: (412) 383-8096. E-mail:
lkane{at}pitt.edu.
Molecular and Cellular Biology, March 2006, p. 2327-2336, Vol. 26, No. 6
0022-538X/06/$08.00+0 doi:10.1128/MCB.26.6.2327-2336.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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