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Molecular and Cellular Biology, November 2000, p. 8409-8419, Vol. 20, No. 22
Vollum Institute1 and
Department of Cell and Developmental
Biology,2 Oregon Health Sciences University,
Portland, Oregon 97201; Department of Pathology and Center for
Immunology, Washington University School of Medicine, St. Louis,
Missouri 631103; and Department of
Medicine and Pathology, University of Chicago, Chicago, Illinois
606374
Received 3 January 2000/Returned for modification 02 May
2000/Accepted 29 August 2000
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.
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
CD28 and the Tyrosine Kinase Lck Stimulate Mitogen-Activated
Protein Kinase Activity in T Cells via Inhibition of the Small G
Protein Rap1
*
Corresponding author. Mailing address: Vollum
Institute, L-474, Oregon Health Sciences University, 3181 SW Sam
Jackson Park Rd., Portland, OR 97201-3098. Phone: (503) 494-4976. Fax:
(503) 494-5494. E-mail: stork{at}ohsu.edu.
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