The transmembrane adapter protein SIT regulates thymic development and peripheral T-cell functions.

Journal:

Mol. Cell. Biol. 2005 Sep

Authors:

Simeoni L, Posevitz V, Kölsch U, Meinert I, Bruyns E, Pfeffer K, Reinhold D, Schraven B

Abstract

SIT is a transmembrane adapter protein that modulates signals emanating from the T-cell receptor (TCR). Here, we have used gene-targeted mice to assess the role of SIT for T-cell development and peripheral T-cell functions. SIT(-/-) double-positive thymocytes show an upregulation of the activation markers CD5 and CD69, suggesting that SIT negatively regulates TCR-mediated signals at the CD4(+) CD8(+) stage of thymic development. This assumption is further supported by the observation that in fem
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ale H-Y TCR transgenic mice, positive selection is enhanced and even converted to negative selection. Similarly, mature peripheral T cells are hyperresponsive towards TCR-mediated stimuli and produce larger amounts of T-helper 1 (TH1) cytokines, and SIT-deficient mice show an increased susceptibility to develop experimental autoimmune encephalomyelitis, a mouse model of multiple sclerosis. These results demonstrate that SIT is a critical negative regulator of TCR-mediated signaling and finely tunes the signals required for thymic selection and peripheral T-cell activation.[less]

Mesh Headings:

Adaptor Proteins, Signal Transducing, Animals, B-Lymphocytes, Cell Differentiation, Lymph Nodes, Membrane Proteins, Mice, Mice, Transgenic, Receptors, Antigen, T-Cell, T-Lymphocytes, Thymus Gland, Up-Regulation