LAT: a T lymphocyte adapter protein that couples the antigen receptor to downstream signaling pathways

Bioessays. 2004 Jan;26(1):61-7. doi: 10.1002/bies.10384.

Abstract

Adapter molecules in a variety of signal transduction systems link receptors to a limited number of commonly used downstream signaling pathways. During T-cell development and mature T-cell effector function, a multichain receptor (the pre-T-cell antigen receptor or the T-cell antigen receptor) activates several protein tyrosine kinases. Receptor and kinase activation is linked to distal signaling pathways (PLC-gamma1 activation, Ca2+ influx, PKC activation and Ras/Erk activation) via the adapter protein LAT (Linker for Activation of T cells). Structure/function studies of LAT including expression of selected LAT point mutations in vivo reveals that these multiple pathways are integrated at the level of the LAT adapter. These studies suggest that similar levels of control may be found in other systems where adapter molecules are known to have important functions.

Publication types

  • Review

MeSH terms

  • Adaptor Proteins, Signal Transducing*
  • Animals
  • Calcium / metabolism
  • Carrier Proteins / physiology*
  • Enzyme Activation
  • Humans
  • Lymphocyte Activation
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Phospholipase C gamma
  • Phosphoproteins / physiology*
  • Point Mutation
  • Protein Kinase C / metabolism
  • Signal Transduction*
  • Structure-Activity Relationship
  • T-Lymphocytes / physiology*
  • Time Factors
  • Type C Phospholipases / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • LAT protein, human
  • Lat protein, mouse
  • Membrane Proteins
  • Phosphoproteins
  • Protein Kinase C
  • Type C Phospholipases
  • Phospholipase C gamma
  • Calcium