Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/124020
Title: Excitotoxic inactivation of constitutive oxidative stress detoxification pathway in neurons can be rescued by PKD1
Author: Pose Utrilla, Julia
García Guerra, Lucía
Puerto, Ana Del
Martín, Abraham
Jurado Arjona, Jerónimo
León Reyes, Noelia S. De
Gamir Morralla, Andrea
Sebastián Serrano, Álvaro
García Gallo, Mónica
Kremer, Leonor
Fielitz, Jens
Ireson, Christofer
Pérez Álvarez, Mª José
Ferrer, Isidro (Ferrer Abizanda)
Hernández, Félix
Avila, Jesús
Lasa, Marina
Campanero, Miguel R.
Iglesias, Teresa
Keywords: Estrès oxidatiu
Malalties neurodegeneratives
Oxidative stress
Neurodegenerative diseases
Issue Date: 22-Dec-2017
Publisher: Nature Publishing Group
Abstract: Excitotoxicity, a critical process in neurodegeneration, induces oxidative stress and neuronal death through mechanisms largely unknown. Since oxidative stress activates protein kinase D1 (PKD1) in tumor cells, we investigated the effect of excitotoxicity on neuronal PKD1 activity. Unexpectedly, we find that excitotoxicity provokes an early inactivation of PKD1 through a dephosphorylation-dependent mechanism mediated by protein phosphatase-1 (PP1) and dual specificity phosphatase-1 (DUSP1). This step turns off the IKK/NF-kappa B/SOD2 antioxidant pathway. Neuronal PKD1 inactivation by pharmacological inhibition or lentiviral silencing in vitro, or by genetic inactivation in neurons in vivo, strongly enhances excitotoxic neuronal death. In contrast, expression of an active dephosphorylation-resistant PKD1 mutant potentiates the IKK/NF-kappa B/SOD2 oxidative stress detoxification pathway and confers neuroprotection from in vitro and in vivo excitotoxicity. Our results indicate that PKD1 inactivation underlies excitotoxicity-induced neuronal death and suggest that PKD1 inactivation may be critical for the accumulation of oxidation-induced neuronal damage during aging and in neurodegenerative disorders.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1038/s41467-017-02322-5
It is part of: Nature Communications, 2017, vol. 8
URI: http://hdl.handle.net/2445/124020
Related resource: http://dx.doi.org/10.1038/s41467-017-02322-5
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Patologia i Terapèutica Experimental)

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