Blocking of melatonin synthesis and MT(1) receptor impairs the activation of Jurkat T cells

Cell Mol Life Sci. 2010 Sep;67(18):3163-72. doi: 10.1007/s00018-010-0374-y. Epub 2010 May 4.

Abstract

Melatonin has been proposed as regulating the immune system by affecting cytokine production in immunocompetent cells, enhancing the production of several T helper (Th)1 cytokines. To further investigate the melatonin's role in IL-2/IL-2R system, we established an inducible T-REx expression system in Jurkat cells in which the protein levels of HIOMT enzyme or MT(1) receptor were significantly down-regulated upon tetracycline incubation. We found that T-REx Jurkat cells with lower levels of HIOMT activity, and consequently lower content of endogenous melatonin, showed IL-2 production decrease after activation with lectin. Likewise, tetracycline-inducible stable cell line expressing MT(1) antisense produced decreased amounts of IL-2 (mRNA and protein levels) after stimulation. Moreover, in T-Rex-MT(1) cells incubated with tetracycline, a sub-optimal PHA dose failed to induce the early activation marker CD25 on the cell surface. The results shown here support the relevance of endogenous melatonin and its signaling in T cell activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylserotonin O-Methyltransferase / antagonists & inhibitors
  • Acetylserotonin O-Methyltransferase / genetics
  • Humans
  • Interleukin-2 / biosynthesis
  • Jurkat Cells
  • Lymphocyte Activation*
  • Melatonin / antagonists & inhibitors*
  • Melatonin / biosynthesis
  • Receptor, Melatonin, MT1 / antagonists & inhibitors*
  • Receptor, Melatonin, MT1 / genetics
  • Signal Transduction
  • T-Lymphocytes / immunology*

Substances

  • Interleukin-2
  • Receptor, Melatonin, MT1
  • Acetylserotonin O-Methyltransferase
  • Melatonin