The ADAP/SKAP55 Signaling Module Regulates T-Cell Receptor-Mediated Integrin Activation through Plasma Membrane Targeting of Rap1

Author:

Kliche Stefanie1,Breitling Dennis1,Togni Mauro1,Pusch Rico1,Heuer Katja2,Wang Xiaoqian1,Freund Christian2,Kasirer-Friede Ana3,Menasche Gael4,Koretzky Gary A.4,Schraven Burkhart1

Affiliation:

1. Institute of Immunology, Otto von Guericke University, 39120 Magdeburg, Germany

2. Protein Engineering Group, Forschungsinstitut für Molekulare Pharmakologie an der Freien Universität Berlin, 13125 Berlin, Germany

3. Division of Hematology/Oncology, University of California, San Diego, La Jolla, California 92093

4. Abramson Family Cancer Research Institute, Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Abstract

ABSTRACT Adhesion of T cells after stimulation of the T-cell receptor (TCR) is mediated via signaling processes that have collectively been termed inside-out signaling. The molecular basis for inside-out signaling is not yet completely understood. Here, we show that a signaling module comprising the cytosolic adapter proteins ADAP and SKAP55 is involved in TCR-mediated inside-out signaling and, moreover, that the interaction between ADAP and SKAP55 is mandatory for integrin activation. Disruption of the ADAP/SKAP55 module leads to displacement of the small GTPase Rap1 from the plasma membrane without influencing its GTPase activity. These findings suggest that the ADAP/SKAP55 complex serves to recruit activated Rap1 to the plasma membrane. In line with this hypothesis is the finding that membrane targeting of the ADAP/SKAP55 module induces T-cell adhesion in the absence of TCR-mediated stimuli. However, it appears as if the ADAP/SKAP55 module can exert its signaling function outside of the classical raft fraction of the cell membrane.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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