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SC79 protects dopaminergic neurons from oxidative stress

Oxidative stress could lead to dopaminergic neuronal cell death. SC79 is a novel, selective and highly-efficient Akt activator. The current study tested its effect in dopaminergic neurons with oxidative stress. In both SH-SY5Y cells and primary murine dopaminergic neurons, pre-treatment with SC79 la...

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Detalles Bibliográficos
Autores principales: Xu, Yan, Gao, Ya-Wen, Yang, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849161/
https://www.ncbi.nlm.nih.gov/pubmed/29560097
http://dx.doi.org/10.18632/oncotarget.23538
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author Xu, Yan
Gao, Ya-Wen
Yang, Yu
author_facet Xu, Yan
Gao, Ya-Wen
Yang, Yu
author_sort Xu, Yan
collection PubMed
description Oxidative stress could lead to dopaminergic neuronal cell death. SC79 is a novel, selective and highly-efficient Akt activator. The current study tested its effect in dopaminergic neurons with oxidative stress. In both SH-SY5Y cells and primary murine dopaminergic neurons, pre-treatment with SC79 largely inhibited hydrogen peroxide (H(2)O(2))-induced cell viability reduction, apoptosis and necrosis. SC79 activated Akt in the neuronal cells, which was required for its neuroprotection against H(2)O(2). Inhibition of Akt activation (by MK-2206 or AT7867) or expression (by targeted short hairpin RNA) largely attenuated SC79-induced neuroprotection. Further, CRISPR-Cas9-mediated Akt1 knockout in SH-SY5Y cells abolished SC79-induced neuroprotective function against H2O2. Reversely, forced activation of Akt by the constitutively-active Akt1 mimicked SC79-induced anti-H(2)O(2) activity. Together, we conclude that activation of Akt by SC79 protects dopaminergic neurons from H(2)O(2).
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spelling pubmed-58491612018-03-20 SC79 protects dopaminergic neurons from oxidative stress Xu, Yan Gao, Ya-Wen Yang, Yu Oncotarget Research Paper Oxidative stress could lead to dopaminergic neuronal cell death. SC79 is a novel, selective and highly-efficient Akt activator. The current study tested its effect in dopaminergic neurons with oxidative stress. In both SH-SY5Y cells and primary murine dopaminergic neurons, pre-treatment with SC79 largely inhibited hydrogen peroxide (H(2)O(2))-induced cell viability reduction, apoptosis and necrosis. SC79 activated Akt in the neuronal cells, which was required for its neuroprotection against H(2)O(2). Inhibition of Akt activation (by MK-2206 or AT7867) or expression (by targeted short hairpin RNA) largely attenuated SC79-induced neuroprotection. Further, CRISPR-Cas9-mediated Akt1 knockout in SH-SY5Y cells abolished SC79-induced neuroprotective function against H2O2. Reversely, forced activation of Akt by the constitutively-active Akt1 mimicked SC79-induced anti-H(2)O(2) activity. Together, we conclude that activation of Akt by SC79 protects dopaminergic neurons from H(2)O(2). Impact Journals LLC 2017-12-20 /pmc/articles/PMC5849161/ /pubmed/29560097 http://dx.doi.org/10.18632/oncotarget.23538 Text en Copyright: © 2018 Xu et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Xu, Yan
Gao, Ya-Wen
Yang, Yu
SC79 protects dopaminergic neurons from oxidative stress
title SC79 protects dopaminergic neurons from oxidative stress
title_full SC79 protects dopaminergic neurons from oxidative stress
title_fullStr SC79 protects dopaminergic neurons from oxidative stress
title_full_unstemmed SC79 protects dopaminergic neurons from oxidative stress
title_short SC79 protects dopaminergic neurons from oxidative stress
title_sort sc79 protects dopaminergic neurons from oxidative stress
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849161/
https://www.ncbi.nlm.nih.gov/pubmed/29560097
http://dx.doi.org/10.18632/oncotarget.23538
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