The POSH/JIP-1 scaffold network regulates TCR-mediated JNK1 signals and effector function in CD8(+) T cells

Eur J Immunol. 2013 Dec;43(12):3361-71. doi: 10.1002/eji.201343635. Epub 2013 Sep 10.

Abstract

Signals from the T-cell recognition of antigen program effector functions are necessary to clear infections and tumors. The JNK pathway is critically important in regulating this process. In T lymphocytes, JNK1 and JNK2 have distinct functions depending on their maturation state and cell-type. However, the mechanisms that regulate their isoform-specific activity and function are still unclear. Here, we identify plenty of SH3 (POSH) and JNK-interacting protein 1 (JIP-1) as a multiprotein scaffold network for TCR-mediated JNK1 activation in CD8(+) T cells. Disruption of the POSH/JIP-1 complex led to profound defects in the activation of JNK1, as well as deficient activation or induction of the transcription factors c-Jun, T-bet, and Eomesodermin. Furthermore, disruption of the POSH/JIP complex in CD8(+) T cells resulted in impaired proliferation, decreased cytokine expression, and the inability to control tumors. Collectively, these data identify a mechanism for the specific regulation of TCR-dependent JNK1 activation and function that is key for CD8(+) T-cell responses.

Keywords: CD8+ T cells; Immune responses; Molecular immunology; Signal transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / immunology*
  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Proliferation*
  • Cytokines / genetics
  • Cytokines / immunology
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / immunology*
  • Enzyme Activation / genetics
  • Enzyme Activation / immunology
  • Mice
  • Mice, Knockout
  • Mitogen-Activated Protein Kinase 8 / genetics
  • Mitogen-Activated Protein Kinase 8 / immunology*
  • Neoplasms / genetics
  • Neoplasms / immunology*
  • Neoplasms / pathology
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / immunology

Substances

  • Adaptor Proteins, Signal Transducing
  • Cytokines
  • Cytoskeletal Proteins
  • Eomes protein, mouse
  • Mapk8ip protein, mouse
  • Sh3md2 protein, mouse
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Mitogen-Activated Protein Kinase 8