FasL expression in activated T lymphocytes involves HuR-mediated stabilization

J Biol Chem. 2010 Oct 8;285(41):31130-8. doi: 10.1074/jbc.M110.137919. Epub 2010 Jul 30.

Abstract

A prolonged activation of the immune system is one of the main causes of hyperproliferation of lymphocytes leading to defects in immune tolerance and autoimmune diseases. Fas ligand (FasL), a member of the TNF superfamily, plays a crucial role in controlling this excessive lymphoproliferation by inducing apoptosis in T cells leading to their rapid elimination. Here, we establish that posttranscriptional regulation is part of the molecular mechanisms that modulate FasL expression, and we show that in activated T cells FasL mRNA is stable. Our sequence analysis indicates that the FasL 3'-untranslated region (UTR) contains two AU-rich elements (AREs) that are similar in sequence and structure to those present in the 3'-UTR of TNFα mRNA. Through these AREs, the FasL mRNA forms a complex with the RNA-binding protein HuR both in vitro and ex vivo. Knocking down HuR in HEK 293 cells prevented the phorbol 12-myristate 13-acetate-induced expression of a GFP reporter construct fused to the FasL 3'-UTR. Collectively, our data demonstrate that the posttranscriptional regulation of FasL mRNA by HuR represents a novel mechanism that could play a key role in the maintenance and proper functioning of the immune system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions*
  • Antigens, Surface / genetics
  • Antigens, Surface / immunology
  • Antigens, Surface / metabolism*
  • Apoptosis / genetics
  • Apoptosis / immunology
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / metabolism
  • Carcinogens / pharmacology
  • ELAV Proteins
  • ELAV-Like Protein 1
  • Fas Ligand Protein / biosynthesis*
  • Fas Ligand Protein / genetics
  • Fas Ligand Protein / immunology
  • Gene Expression Regulation*
  • Humans
  • Immune Tolerance / drug effects
  • Immune Tolerance / genetics
  • Immune Tolerance / immunology
  • Jurkat Cells
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • RNA Stability*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / immunology
  • RNA-Binding Proteins / metabolism*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • 3' Untranslated Regions
  • Antigens, Surface
  • Carcinogens
  • ELAV Proteins
  • ELAV-Like Protein 1
  • ELAVL1 protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • RNA-Binding Proteins
  • Tetradecanoylphorbol Acetate