Regulation of proximal T cell receptor signaling and tolerance induction by deubiquitinase Usp9X

J Exp Med. 2014 Sep 22;211(10):1947-55. doi: 10.1084/jem.20140860. Epub 2014 Sep 8.

Abstract

The T cell hyperproliferation and autoimmune phenotypes that manifest in mice lacking E3 ubiquitin ligases such as Cbl, ITCH, or GRAIL highlight the importance of ubiquitination for the maintenance of peripheral T cell tolerance. Less is known, however, about the deubiquitinating enzymes that regulate T cell proliferation and effector function. Here, we define a cell intrinsic role for the deubiquitinase Usp9X during proximal TCR signaling. Usp9X-deficient T cells were hypoproliferative, yet mice with T cell-specific Usp9x deletion had elevated numbers of antigen-experienced T cells and expanded PD-1 and OX40-expressing populations consistent with immune hyperactivity. Aged Usp9x KO mice developed lupus-like autoimmunity and lymphoproliferative disease, indicating that ubiquitin ligases and deubiquitinases maintain the delicate balance between effective immunity and self-tolerance.

MeSH terms

  • Animals
  • Autoimmunity / genetics*
  • Calcium / metabolism
  • Cell Proliferation
  • DNA Primers / genetics
  • Endopeptidases / genetics
  • Endopeptidases / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Gene Knockdown Techniques
  • Lymphocytes / metabolism
  • Lymphoproliferative Disorders / genetics*
  • Mice
  • Mice, Knockout
  • RNA, Small Interfering / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Self Tolerance / genetics
  • Self Tolerance / immunology*
  • Signal Transduction / immunology*
  • Ubiquitin Thiolesterase

Substances

  • DNA Primers
  • RNA, Small Interfering
  • Receptors, Antigen, T-Cell
  • Endopeptidases
  • Ubiquitin Thiolesterase
  • Usp9x protein, mouse
  • Calcium