Differential localization and function of ADP-ribosylation factor-6 in anergic human T cells: a potential marker for their identification

J Immunol. 2003 Aug 15;171(4):1691-6. doi: 10.4049/jimmunol.171.4.1691.

Abstract

Anergy is a state of immunologic tolerance in which T cells are viable but incapable of responding to antigenic stimulation. Recent data indicate that anergic cells have a distinct gene expression program that determines their unique function. In this study we show that anergic human T cells selectively express the small GTPase ADP-ribosylation factor-6 (ARF6), which is involved in membrane traffic and regulation of the cortical actin cytoskeleton. ARF6 was expressed in the GTP-bound form that localizes at the plasma membrane, resulting in a distinct morphologic appearance of anergic cells. Forced expression of ARF6-GTP in Jurkat T cells prevented TCR-mediated reorganization of cortical actin, extracellular signal-regulated kinase1/2 activation, and IL-2 transcription. Forced expression of ARF6-GTP in primary human T cells inhibited extracellular signal-regulated kinase1/2 activation and proliferative responses. Importantly, T cells with the distribution pattern of ARF6-GTP were detected in peripheral blood, suggesting that anergic T cells may constitutively exist in vivo.

Publication types

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

MeSH terms

  • ADP-Ribosylation Factor 6
  • ADP-Ribosylation Factors / biosynthesis
  • ADP-Ribosylation Factors / blood
  • ADP-Ribosylation Factors / metabolism*
  • ADP-Ribosylation Factors / physiology*
  • Actins / antagonists & inhibitors
  • Actins / metabolism
  • Biomarkers / analysis
  • Cell Membrane / genetics
  • Cell Membrane / immunology
  • Cell Membrane / metabolism
  • Clonal Anergy / genetics
  • Clonal Anergy / immunology*
  • Clone Cells
  • Enzyme Activation / genetics
  • Enzyme Activation / immunology
  • Genetic Vectors
  • Guanosine Triphosphate / genetics
  • Guanosine Triphosphate / metabolism
  • Humans
  • Interleukin-2 / antagonists & inhibitors
  • Interleukin-2 / genetics
  • Interleukin-2 / metabolism
  • Jurkat Cells
  • Membrane Proteins / blood
  • Mitogen-Activated Protein Kinase 1 / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism
  • Protein Binding / genetics
  • Protein Binding / immunology
  • RNA, Messenger / biosynthesis
  • Receptors, Antigen, T-Cell / antagonists & inhibitors
  • Receptors, Antigen, T-Cell / physiology
  • T-Lymphocyte Subsets / enzymology
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism*
  • Transcription, Genetic / immunology
  • Transfection

Substances

  • ADP-Ribosylation Factor 6
  • Actins
  • Biomarkers
  • Interleukin-2
  • Membrane Proteins
  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • Guanosine Triphosphate
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • ADP-Ribosylation Factors
  • ARF6 protein, human