Positive Regulation of T Cell Activation and Integrin Adhesion by the Adapter Fyb/Slap

Author:

Griffiths Emily K.12,Krawczyk Connie12,Kong Young-Yun12,Raab Monika3,Hyduk Sharon J.4,Bouchard Denis1,Chan Vera S.2,Kozieradzki Ivona12,Oliveira-dos-Santos Antonio J.12,Wakeham Andrew1,Ohashi Pamela S.2,Cybulsky Myron I.4,Rudd Christopher E.3,Penninger Josef M.12

Affiliation:

1. Amgen Institute, 620 University Avenue, Toronto, Ontario, Canada M5G 2C1.

2. Ontario Cancer Institute, University Health Network, and Departments of Medical Biophysics and Immunology, University of Toronto, 610 University Avenue, Toronto, Ontario, Canada M5G 2M9.

3. Division of Tumor Immunology, Dana-Farber Cancer Institute, and Departments of Pathology and Medicine, Harvard Medical School, Boston, MA 02115, USA.

4. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto General Hospital Research Institute, Toronto, Canada.

Abstract

The molecular adapter Fyb/Slap regulates signaling downstream of the T cell receptor (TCR), but whether it plays a positive or negative role is controversial. We demonstrate that Fyb/Slap-deficient T cells exhibit defective proliferation and cytokine production in response to TCR stimulation. Fyb/Slap is also required in vivo for T cell–dependent immune responses. Functionally, Fyb/Slap has no apparent role in the activation of known TCR signaling pathways, F-actin polymerization, or TCR clustering. Rather, Fyb/Slap regulates TCR-induced integrin clustering and adhesion. Thus, Fyb/Slap is the first molecular adapter to be identified that couples TCR stimulation to the avidity modulation of integrins governing T cell adhesion.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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