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The role of Syk in peripheral T cells.


ABSTRACT: The aim of this study was to understand how Syk affects peripheral T cell function. T cells from Syk-/- chimeric mice and DR1 Sykfl/fl CD4cre conditional mice gave strong CD3-induced Th1, Th2, and Th17 cytokine responses. However, an altered peptide ligand (APL) of human CII (256-276) with two substitutions (F263N, E266D), also called A12, elicited only Th2 cytokine responses from Sykfl/fl T cells but not Sykfl/fl-CD4cre T cells. Western blots revealed a marked increase in the phosphorylation of Syk, JNK and p38 upon A12/DR1 activation in WT or Sykfl/fl T cells but not in Sykfl/flCD4-cre cells. We demonstrate that Syk is required for the APL- induction of suppressive cytokines. Chemical Syk inhibitors blocked activation of GATA-3 by peptide A12/DR1. In conclusion, this study provides novel insights into the role that Syk plays in directing T cell activity, and may shape therapeutic approaches for autoimmune diseases.

SUBMITTER: Park JE 

PROVIDER: S-EPMC6350940 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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The aim of this study was to understand how Syk affects peripheral T cell function. T cells from Syk<sup>-/-</sup> chimeric mice and DR1 Syk<sup>fl/fl</sup> CD4<sup>cre</sup> conditional mice gave strong CD3-induced Th1, Th2, and Th17 cytokine responses. However, an altered peptide ligand (APL) of human CII (256-276) with two substitutions (F263N, E266D), also called A12, elicited only Th2 cytokine responses from Syk<sup>fl/fl</sup> T cells but not Syk<sup>fl/fl-</sup>CD4<sup>cre</sup> T cells.  ...[more]

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