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.
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Zimmer, E.R., Leuzy, A., Souza, D.O. et al. Inhibition of Protein Phosphatase 2A: Focus on the Glutamatergic System. Mol Neurobiol 53, 3753–3755 (2016). https://doi.org/10.1007/s12035-015-9321-0
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DOI: https://doi.org/10.1007/s12035-015-9321-0