Contact-Dependent T Cell Activation and T Cell Stopping Require Talin1
Author(s) -
Sarah A. Wernimont,
Andrew J. Wiemer,
David A. Bennin,
Susan J. Monkley,
Thomas Ludwig,
David R. Critchley,
Anna Huttenlocher
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1102028
Subject(s) - microbiology and biotechnology , t cell , immunological synapse , actin , immune system , biology , immunology , t cell receptor
T cell-APC contact initiates T cell activation and is maintained by the integrin LFA-1. Talin1, an LFA-1 regulator, localizes to the immune synapse (IS) with unknown roles in T cell activation. In this study, we show that talin1-deficient T cells have defects in contact-dependent T cell stopping and proliferation. Although talin1-deficient T cells did not form stable interactions with APCs, transient contacts were sufficient to induce signaling. In contrast to prior models, LFA-1 polarized to T cell-APC contacts in talin1-deficient T cells, but vinculin and F-actin polarization at the IS was impaired. These results indicate that T cell proliferation requires sustained, talin1-mediated T cell-APC interactions and that talin1 is necessary for F-actin polarization and the stability of the IS.
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