Abstract

The T cell specific adapter protein (TSAd) is expressed in activated T cells and NK cells. While TSAd is beginning to emerge as a critical regulator of Lck and Itk activity in T cells, its role in NK cells has not yet been explored. Here we have examined susceptibility to virus infections in a murine model using various viral infection models. We report that TSAd-deficient mice display reduced clearance of murine cytomegalovirus (MCMV) that lack the viral MHC class I homologue m157, which is critical for Ly49H-mediated NK cell recognition of infected cells. In this infection model, NK cells contribute in the early stages of the disease, whereas CD8+ T cells are critical for viral clearance. We found that mice infected with MCMV Δm157 displayed reduced viral clearance in the spleen as well as reduced proliferation in spleen NK cells and CD8+ T cells in the absence of TSAd. Though no other immunophenotype was detected in the infection models tested, these data suggests that in the absence of the Ly49H ligand activation, NK cell and CD8+ T cell responses may be compromised in TSAd-deficient mice.

Highlights

  • The T cell specific adapter protein (TSAd) is expressed in activated T cells and NK cells

  • We report that TSAd-deficient mice display reduced clearance of murine cytomegalovirus (MCMV) that lack the viral MHC class I homologue m157, which is critical for Ly49H-mediated NK cell recognition of infected cells

  • The mouse NK cells displayed a rapid increase in TSAd expression, evident as early as 10 minutes following PMA/ionomycin stimulation indicating that the expression of TSAd is regulated at the translational level as reported earlier[29]

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Summary

Introduction

The T cell specific adapter protein (TSAd) is expressed in activated T cells and NK cells. We report that TSAd-deficient mice display reduced clearance of murine cytomegalovirus (MCMV) that lack the viral MHC class I homologue m157, which is critical for Ly49H-mediated NK cell recognition of infected cells. In this infection model, NK cells contribute in the early stages of the disease, whereas CD81 T cells are critical for viral clearance. Triggering of the TCR leads to downstream signal propagation through a sequence of phosphorylation events modulated by various adaptor proteins One of these adaptors, encoded by the Sh2d2a gene, is T cell specific adapter protein (TSAd), which is upregulated in activated T cells[1]. Lck and Itk are expressed almost solely in T and NK cells and are important for efficient NK cell cytotoxicity and survival[12,13,14,15,16]

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