Differential impact of L-arginine deprivation on the activation and effector functions of T cells and macrophages

J Leukoc Biol. 2009 Feb;85(2):268-77. doi: 10.1189/jlb.0508310. Epub 2008 Nov 13.

Abstract

The metabolism of the amino acid L-arginine is emerging as a crucial mechanism for the regulation of immune responses. Here, we characterized the impact of L-arginine deprivation on T cell and macrophage (MPhi) effector functions: We show that whereas L-arginine is required unconditionally for T cell activation, MPhi can up-regulate activation markers and produce cytokines and chemokines in the absence of L-arginine. Furthermore, we show that L-arginine deprivation does not affect the capacity of activated MPhi to up-regulate L-arginine-metabolizing enzymes such as inducible NO synthase and arginase 1. Thus, our results show that to exert their effector functions, T cells and MPhi have different requirements for L-arginine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginase / metabolism
  • Arginine / deficiency*
  • Arginine / pharmacology
  • Biomarkers / metabolism
  • Cell Proliferation
  • Cytokines / biosynthesis
  • Female
  • Lymphocyte Activation / immunology*
  • Macrophage Activation / immunology*
  • Macrophages / cytology
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Nitric Oxide / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology*

Substances

  • Biomarkers
  • Cytokines
  • Nitric Oxide
  • Arginine
  • Arginase