Coupling of the TCR to Integrin Activation by SLAP-130/Fyb
- 21 September 2001
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 293 (5538) , 2263-2265
- https://doi.org/10.1126/science.1063486
Abstract
SLAP-130/Fyb (SLP-76–associated phosphoprotein or Fyn-binding protein; also known as Fyb/Slap) is a hematopoietic-specific adapter, which associates with and modulates function of SH2-containing leukocyte phosphoprotein of 76 kilodaltons (SLP-76). T cells from mice lacking SLAP-130/Fyb show markedly impaired proliferation following CD3 engagement. In addition, the T cell receptor (TCR) in SLAP-130/Fyb mutant cells fails to enhance integrin-dependent adhesion. Although TCR-induced actin polymerization is normal, TCR-stimulated clustering of the integrin LFA-1 is defective in SLAP-130/Fyb–deficient cells. These data indicate that SLAP-130/Fyb is important for coupling TCR-mediated actin cytoskeletal rearrangement with activation of integrin function, and for T cells to respond fully to activating signals.Keywords
This publication has 25 references indexed in Scilit:
- Fyn-Binding Protein (Fyb)/Slp-76–Associated Protein (Slap), Ena/Vasodilator-Stimulated Phosphoprotein (Vasp) Proteins and the Arp2/3 Complex Link T Cell Receptor (Tcr) Signaling to the Actin CytoskeletonThe Journal of cell biology, 2000
- The Immunological Synapse: A Molecular Machine Controlling T Cell ActivationScience, 1999
- Requirement for the Leukocyte-Specific Adapter Protein SLP-76 for Normal T Cell DevelopmentScience, 1998
- Uncoupling of Nonreceptor Tyrosine Kinases from PLC-γ1 in an SLP-76-Deficient T CellScience, 1998
- LFA-1–mediated Adhesion Is Regulated by Cytoskeletal Restraint and by a Ca2+-dependent Protease, CalpainThe Journal of cell biology, 1998
- LATCell, 1998
- LFA-1-deficient mice show normal CTL responses to virus but fail to reject immunogenic tumor.The Journal of Experimental Medicine, 1996
- Extracellular Ca2+ modulates leukocyte function-associated antigen-1 cell surface distribution on T lymphocytes and consequently affects cell adhesionThe Journal of cell biology, 1994
- Enhancement of LFA-1-mediated cell adhesion by triggering through CD2 or CD3 on T lymphocytesNature, 1989
- T-cell receptor cross-linking transiently stimulates adhesiveness through LFA-1Nature, 1989