P2X7 receptors regulate NKT cells in autoimmune hepatitis

J Immunol. 2006 Feb 15;176(4):2152-60. doi: 10.4049/jimmunol.176.4.2152.

Abstract

Adenine nucleotides induce danger signals in T cells via purinergic receptors, raising the question whether they exert similar effects on innate immunity. Here we show that micromolar concentrations of nicotinamide adenine dinucleotide (NAD) induce a rapid increase of annexin V staining in NKT cells in vitro, a response that requires expression of P2X(7)Rs. Consistent with this result, treatment of mice with NAD causes a temporary decrease of NKT cells in the liver and protects from Con A- and alpha-galactosylceramide-induced hepatitis, both of which require functional NKT cells. Resistance to liver injury is associated with decreased cytokine production by NKT cells in NAD-treated mice. In contrast, when NAD is injected into Con A- or alpha-galactosylceramide-primed mice, liver injury is exacerbated and cytokine production by NKT cells is increased. This effect is caused by P2X(7)R-mediated stimulation of activated NKT cells. In agreement, mice lacking P2X(7)Rs on lymphocytes suffer reduced liver injury, and animals lacking ADP-ribosyltransferase, the enzyme that uses NAD to attach ADP-ribosyl groups to cell surfaces, are also resistant to Con A-induced hepatitis. These results prompt the conclusion that engagement of P2X(7)Rs on NKT cells inhibits naive, while stimulating activated cells, resulting in suppression or stimulation of autoimmune hepatitis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Annexin A5 / metabolism
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Female
  • Hepatitis, Autoimmune / immunology*
  • Hepatitis, Autoimmune / metabolism*
  • Hepatitis, Autoimmune / prevention & control
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Liver / injuries
  • Liver / metabolism
  • Liver / pathology
  • Lymphocyte Activation
  • Macrolides / metabolism
  • Macrolides / pharmacology
  • Mice
  • Mice, Knockout
  • NAD / pharmacology
  • Receptors, Purinergic P2 / deficiency
  • Receptors, Purinergic P2 / genetics
  • Receptors, Purinergic P2 / metabolism*
  • Receptors, Purinergic P2X7
  • T-Lymphocytes, Regulatory / drug effects
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism*

Substances

  • Annexin A5
  • Cytokines
  • Macrolides
  • P2rx7 protein, mouse
  • Receptors, Purinergic P2
  • Receptors, Purinergic P2X7
  • NAD
  • concanamycin A