Signaling Life and Death in the Thymus: Timing Is Everything
- 21 March 2003
- journal article
- review article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 299 (5614) , 1859-1863
- https://doi.org/10.1126/science.1067833
Abstract
T lymphocytes are generated in the thymus, where developing thymocytes must accept one of two fates: They either differentiate or they die. These fates are chiefly determined by signals that originate from the T cell receptor (TCR), a single receptor complex with a remarkable capacity to decide between distinct cell fates. This review explores TCR signaling in thymocytes and focuses on the kinetic aspects of ligand binding, coreceptor involvement, protein phosphorylation, and mitogen-activated protein kinase (MAPK) activation. Understanding the logic of TCR signaling may eventually explain how thymocytes and T cells distinguish self from nonself, a phenomenon that has fascinated immunologists for 50 years.Keywords
This publication has 64 references indexed in Scilit:
- The Src-like Adaptor Protein Downregulates the T Cell Receptor on CD4+CD8+ Thymocytes and Regulates Positive SelectionImmunity, 2001
- RasGRP, a Ras Guanyl Nucleotide- Releasing Protein with Calcium- and Diacylglycerol-Binding MotifsScience, 1998
- A Motif within the T Cell Receptor α Chain Constant Region Connecting Peptide Domain Controls Antigen ResponsivenessImmunity, 1996
- Opposing Effects of ERK and JNK-p38 MAP Kinases on ApoptosisScience, 1995
- Kinetic proofreading in T-cell receptor signal transduction.Proceedings of the National Academy of Sciences, 1995
- Serial triggering of many T-cell receptors by a few peptide–MHC complexesNature, 1995
- Positive Selection of ThymocytesAnnual Review of Immunology, 1995
- Positive and Negative Thymocyte Selection Induced by Different Concentrations of a Single PeptideScience, 1994
- The thymus selects the useful, neglects the useless and destroys the harmfulImmunology Today, 1989
- The CD4 and CD8 T cell surface antigens are associated with the internal membrane tyrosine-protein kinase p56lckCell, 1988