A novel functional interaction between Vav and PKCtheta is required for TCR-induced T cell activation

Immunity. 2000 Feb;12(2):151-60. doi: 10.1016/s1074-7613(00)80168-5.

Abstract

Vav and PKCtheta play an early and important role in the TCR/CD28-induced stimulation of MAP kinases and activation of the IL-2 gene. Vav is also essential for actin cytoskeleton reorganization and TCR capping. Here, we report that PKCtheta function was selectively required in a Vav signaling pathway that mediates the TCR/CD28-induced activation of JNK and the IL-2 gene and the upregulation of CD69 expression. Vav also promoted PKCtheta translocation from the cytosol to the membrane and cytoskeleton and induced its enzymatic activation in a CD3/CD28-initiated pathway that was dependent on Rac and on actin cytoskeleton reorganization. These findings reveal that the Vav/Rac pathway promotes the recruitment of PKCtheta to the T cell synapse and its activation, essential processes for T cell activation and IL-2 production.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / metabolism
  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, T-Lymphocyte / metabolism
  • Biological Transport
  • CD28 Antigens / metabolism*
  • Cell Cycle Proteins*
  • Cell Membrane / metabolism
  • Enzyme Activation
  • Gene Expression Regulation
  • Humans
  • Interleukin-2 / genetics
  • Isoenzymes / metabolism*
  • Isoenzymes / physiology
  • JNK Mitogen-Activated Protein Kinases
  • Jurkat Cells
  • Lectins, C-Type
  • Lymphocyte Activation*
  • Mitogen-Activated Protein Kinases / metabolism
  • Protein Kinase C / metabolism*
  • Protein Kinase C / physiology
  • Protein Kinase C-theta
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-vav
  • Rabbits
  • Receptors, Antigen, T-Cell / metabolism*
  • T-Lymphocytes / immunology*
  • Transcriptional Activation
  • Up-Regulation
  • rac GTP-Binding Proteins / metabolism

Substances

  • Actins
  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD28 Antigens
  • CD69 antigen
  • Cell Cycle Proteins
  • Interleukin-2
  • Isoenzymes
  • Lectins, C-Type
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-vav
  • Receptors, Antigen, T-Cell
  • VAV1 protein, human
  • PRKCQ protein, human
  • Protein Kinase C
  • Protein Kinase C-theta
  • JNK Mitogen-Activated Protein Kinases
  • Mitogen-Activated Protein Kinases
  • rac GTP-Binding Proteins