Autoantibody-mediated cytotoxicity in paediatric opsoclonus-myoclonus syndrome is dependent on ERK-1/2 phophorylation

J Neuroimmunol. 2015 Dec 15:289:182-6. doi: 10.1016/j.jneuroim.2015.10.022. Epub 2015 Oct 30.

Abstract

Paediatric opsoclonus-myoclonus syndrome (OMS) is in 50% of the cases associated with a neuroblastoma as a paraneoplastic syndrome and is associated with surface-binding antibodies against cerebellar granular neurons (CGN). To evaluate possible pathogenic effects of these autoantibodies on CGN we examined their influence on the MAPKinase enzymes ERK-1/2 and p38 using flow cytometry and phospho-specific antibodies. OMS IgG but not IgG from neuroblastoma without OMS or healthy controls induced phosphorylation of ERK-1/2 in cerebellar granular neurons (p<0.01). No effect on p38 phosphorylation or on HEK293 control cell line could be detected. IgG-mediated phosphorylation of ERK-1/2 was associated with an increased cytotoxicity of CGN, which could be blocked by ERK-1/2 pathway inhibitor U0126. We here show that IgG-mediated anti-neuronal cytotoxicity in OMS is mediated by ERK-1/2 phosphorylation in CGN.

Keywords: Autoantibodies; Neuroblastoma; Opsoclonus-myoclonus syndrome; Paraneoplastic neurological syndrome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantibodies / immunology*
  • Autoantibodies / pharmacology
  • Butadienes / pharmacology
  • Cerebellum / cytology
  • Enzyme Inhibitors / pharmacology
  • Female
  • Flow Cytometry
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • MAP Kinase Signaling System / physiology
  • Male
  • Mitogen-Activated Protein Kinases / immunology*
  • Mitogen-Activated Protein Kinases / metabolism*
  • Neurons / drug effects
  • Neurons / metabolism
  • Nitriles / pharmacology
  • Opsoclonus-Myoclonus Syndrome / immunology*
  • Opsoclonus-Myoclonus Syndrome / metabolism*
  • Phosphorylation
  • Rats
  • Time Factors

Substances

  • Autoantibodies
  • Butadienes
  • Enzyme Inhibitors
  • Nitriles
  • U 0126
  • L-Lactate Dehydrogenase
  • Mitogen-Activated Protein Kinases