期刊
CELLULAR SIGNALLING
卷 18, 期 10, 页码 1647-1654出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2006.01.015
关键词
T-lymphocytes; NF-kappa B; Ras proteins; MAGUK proteins; lymphocyte activation
类别
资金
- NIDDK NIH HHS [P30 DK043351, DK43351, P30 DK040561, P30 DK040561-11] Funding Source: Medline
Nore1A was originally identified as a potential Ras effector, and Nore1B is an alternatively spliced isoform. Both share a Ras/Rap association domain (RA domain) but only Nore1A contains sequence motifs that predict SH3 domain binding and diacylglycerol/phorbol ester binding in the amino-terminal region. Here we report that Carma1 binds to Nore1A and Nore1B through the RA domain and that Carma1 interacts with active Ras in the presence of Note1B. RNA interference against Nore1B attenuates NF-kappa B activation induced by T cell receptor (TCR) ligation, but not NF-kappa B activation induced by TNF alpha or lipoteichoic acid. In addition, Nore1B is also required for KiRas GV12-mediated ERK1 activation and Elk1 reporter activity in T cells. We also provide evidence that knockdown of Nore1B also impairs polarized redistribution of Ras at the B cell-T cell immune interface. Together, these findings suggest that endogenous Nore1B recruits active Ras to the APC-T cell interface and mediates the interaction between Ras and Carma1. (c) 2006 Elsevier Inc. All rights reserved.
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