AI Article Synopsis

  • Themis is crucial for T cell selection, as it determines the balance between positive and negative selection by regulating Shp1 activity.
  • The study found that Themis enhances Shp1’s phosphatase activity through increased phosphorylation in thymocytes, but this effect does not occur in mature T cells.
  • When Shp1 is absent, Themis can interact with Shp2, allowing thymic development to proceed normally in certain knockout mice, but the loss of both Themis and Shp1 results in a thymic development issue similar to that seen when Themis is deleted alone.

Article Abstract

Thymocyte-expressed molecule involved in selection (Themis) has been shown to be important for T cell selection by setting the threshold for positive versus negative selection. Themis interacts with the protein tyrosine phosphatase (PTP) Src-homology domain containing phosphatase-1 (Shp1), a negative regulator of the T cell receptor (TCR) signaling cascade. However, how Themis regulates Shp1 is still not clear. Here, using a very sensitive phosphatase assay on ex vivo thymocytes, we have found that Themis enhances Shp1 phosphatase activity by increasing its phosphorylation. This positive regulation of Shp1 activity by Themis is found in thymocytes, but not in peripheral T cells. Shp1 activity is modulated by different affinity peptide MHC ligand binding in thymocytes. Themis is also associated with phosphatase activity, due to its constitutive interaction with Shp1. In the absence of Shp1 in thymocytes, Themis interacts with Shp2, which leads to almost normal thymic development in Shp1 conditional knockout (cKO) mice. Double deletion of both Themis and Shp1 leads to a thymic phenotype similar to that of Themis KO. These findings demonstrate unequivocally that Themis positively regulates Shp1 phosphatase activity in TCR-mediated signaling in developing thymocytes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275480PMC
http://dx.doi.org/10.1073/pnas.1720209115DOI Listing

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