PKCtheta signals activation versus tolerance in vivo

J Exp Med. 2004 Mar 15;199(6):743-52. doi: 10.1084/jem.20031022.

Abstract

Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology
  • CD28 Antigens / immunology
  • CD28 Antigens / metabolism*
  • CD4 Antigens / immunology
  • Clonal Anergy / immunology
  • Flow Cytometry
  • Immunohistochemistry
  • Isoenzymes / immunology
  • Isoenzymes / metabolism*
  • Lymphocyte Activation / immunology*
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Protein Kinase C / immunology
  • Protein Kinase C / metabolism*
  • Protein Kinase C-theta
  • Signal Transduction / immunology*
  • T-Lymphocytes / immunology*
  • Vesicular stomatitis Indiana virus

Substances

  • CD28 Antigens
  • CD4 Antigens
  • Isoenzymes
  • Prkcq protein, mouse
  • Protein Kinase C
  • Protein Kinase C-theta