Document Type
Article
Publication Date
2000
Abstract
Proliferation of T cells via activation of the T-cell receptor (TCR) requires concurrent engagement of accessory costimulatory molecules to achieve full activation. The best-studied costimulatory molecule, CD28, achieves these effects, in part, by augmenting signals from the TCR to the mitogen-activated protein (MAP) kinase cascade. We show here that TCR-mediated stimulation of MAP kinase extracellular-signal-regulated kinases (ERKs) is limited by activation of the Ras antagonist Rap1. CD28 increases ERK signaling by blocking Rap1 action. CD28 inhibits Rap1 activation because it selectively stimulates an extrinsic Rap1 GTPase activity. The ability of CD28 to stimulate Rap1 GTPase activity was dependent on the tyrosine kinase Lck. Our results suggest that CD28-mediated Rap1 GTPase-activating protein activation can help explain the augmentation of ERKs during CD28 costimulation.
Recommended Citation
Carey, Kendall D.; Dillon, Tara J.; Schmitt, John M.; Baird, Allison M.; Holdorf, Amy D.; Straus, David B.; Shaw, Andrey S.; and Stork, Philip J. S., "CD28 and the Tyrosine Kinase Lck Stimulate Mitogen-Activated Protein Kinase Activity in T Cells via Inhibition of the Small G Protein Rap1" (2000). Faculty Publications - Department of Biological & Molecular Science. 51.
https://digitalcommons.georgefox.edu/bio_fac/51
Comments
Originally published by Molecular and Cellular Biology, 20(22); 8409-8419, 2000.
http://mcb.asm.org/