Secreted phospholipase A(2) group IIA is a neurotoxin released by stimulated human glial cells

Mol Cell Neurosci. 2012 Apr;49(4):430-8. doi: 10.1016/j.mcn.2012.02.006. Epub 2012 Mar 3.

Abstract

Neuroinflammation, which is one of the hallmarks of neurodegenerative disorders such as Alzheimer's disease, involves secretion of pro-inflammatory mediators by activated glial cells. Secreted phospholipase A(2) group IIA (sPLA(2)IIA) has been implicated as an inflammatory mediator contributing to various peripheral inflammatory conditions; however, little is known about the role this enzyme plays in neuroinflammation. Human microglia-like promonocytic THP-1 cells and human primary astrocytes were used to study sPLA(2)IIA expression, secretion and function. Production of sPLA(2)IIA by these cells was induced in response to stimulation by pro-inflammatory mediators at both mRNA and protein levels. Removal of sPLA(2)IIA from stimulated human microglia-like cell and astrocyte supernatants by immunosorbent caused significant reduction of their toxicity towards SH-SY5Y neuroblastoma cells. Both sPLA(2)IIA specific and non-specific PLA(2) inhibitors exhibited no anti-cytotoxic or neuroprotective effects, suggesting that sPLA(2)IIA cytotoxicity is mediated by a non-enzymatic mechanism. The data obtained indicate that sPLA(2)IIA may contribute to the pathogenesis of neurodegenerative diseases involving neuroinflammation. Agents inhibiting the non-enzymatic actions of sPLA(2)IIA could be used to slow down progression of neurodegenerative processes that are driven by inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cells, Cultured
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique
  • Group II Phospholipases A2 / metabolism*
  • Group II Phospholipases A2 / pharmacology
  • Humans
  • Inflammation / metabolism
  • Neuroglia / drug effects
  • Neuroglia / metabolism*
  • Neurons / drug effects*
  • Neurons / metabolism
  • Neurotoxins / metabolism*
  • Recombinant Proteins / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Neurotoxins
  • Recombinant Proteins
  • Group II Phospholipases A2
  • PLA2G2A protein, human