Inhibition of Protein Phosphatase 2A: Focus on the Glutamatergic System

Mol Neurobiol. 2016 Aug;53(6):3753-3755. doi: 10.1007/s12035-015-9321-0. Epub 2015 Jul 4.

Abstract

In a recent review published in Molecular Neurobiology, Kamat and colleagues (Mol Neurobiol. 2014 Dec;50(3):852-65) highlighted the cellular and molecular mechanisms involved in Okadaic acid (OKA)-induced neurotoxicity. In this review, the authors underline a wide range of pathological signaling pathways involved in OKA-induced neurotoxicity; however, the role of glutamate was only briefly described. We believe that the hyperactivation of the glutamatergic system is a key pathophysiological player in OKA-induced neurotoxicity and deserves serious attention. In this commentary, we propose an integrative model linking glutamate and PP2A and put forward some unanswered questions.

Keywords: Excitotoxicity; Glutamate; Okadaic acid; Protein phosphatase 2A; Tau hyperphosphorylation.

Publication types

  • Comment

MeSH terms

  • Animals
  • Enzyme Inhibitors / pharmacology*
  • Glutamic Acid / metabolism*
  • Humans
  • Models, Biological
  • Okadaic Acid / pharmacology
  • Protein Phosphatase 2 / antagonists & inhibitors*
  • Protein Phosphatase 2 / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism

Substances

  • Enzyme Inhibitors
  • Receptors, N-Methyl-D-Aspartate
  • Okadaic Acid
  • Glutamic Acid
  • Protein Phosphatase 2