Signaling life and death in the thymus: timing is everything

Science. 2003 Mar 21;299(5614):1859-63. doi: 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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Antigens / immunology
  • Antigens, CD / immunology
  • Antigens, CD / metabolism
  • Apoptosis*
  • Carrier Proteins / metabolism
  • Cell Differentiation
  • Cell Division
  • Enzyme Activation
  • Humans
  • Ligands
  • MAP Kinase Signaling System
  • Major Histocompatibility Complex / immunology
  • Membrane Proteins*
  • Mitogen-Activated Protein Kinases / metabolism
  • Phosphoproteins / metabolism
  • Receptors, Antigen, T-Cell, alpha-beta / chemistry
  • Receptors, Antigen, T-Cell, alpha-beta / immunology
  • Receptors, Antigen, T-Cell, alpha-beta / physiology*
  • Selection, Genetic
  • Self Tolerance
  • Signal Transduction*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / physiology*
  • Thymus Gland / cytology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens
  • Antigens, CD
  • Carrier Proteins
  • LAT protein, human
  • Ligands
  • Membrane Proteins
  • Phosphoproteins
  • Receptors, Antigen, T-Cell, alpha-beta
  • Mitogen-Activated Protein Kinases