Neuroserpin Attenuates H2O2-Induced Oxidative Stress in Hippocampal Neurons via AKT and BCL-2 Signaling Pathways
Autor: | Nigel P. Birch, Yong Cheng, Y. Peng Loh |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Neurotoxicity General Medicine Biology medicine.disease medicine.disease_cause Molecular biology Neuroprotection Cell biology 03 medical and health sciences Cellular and Molecular Neuroscience chemistry.chemical_compound 030104 developmental biology 0302 clinical medicine chemistry Neuroserpin Trk receptor medicine LY294002 Signal transduction Protein kinase B 030217 neurology & neurosurgery Oxidative stress |
Zdroj: | Journal of Molecular Neuroscience. 61:123-131 |
ISSN: | 1559-1166 0895-8696 |
DOI: | 10.1007/s12031-016-0807-7 |
Popis: | Oxidative stress plays a critical role in neuronal injury and is associated with various neurological diseases. Here, we explored the potential protective effect of neuroserpin against oxidative stress in primary cultured hippocampal neurons. Our results show that neuroserpin inhibits H2O2-induced neurotoxicity in hippocampal cultures as measured by WST, LDH release, and TUNEL assays. We found that neuroserpin enhanced the activation of AKT in cultures subjected to oxidative stress and that the AKT inhibitor Ly294002 blocked this neuroprotective effect. Neuroserpin increased the expression of the anti-apoptotic protein BCL-2 and blocked the activation of caspase-3. Neuroserpin did not increase the level of neuroprotection over levels seen in neurons transduced with a BCL-2 expression vector, and an inhibitor of Trk receptors, K252a, did not block neuroserpin's effect. Taken together, our study demonstrates that neuroserpin protects against oxidative stress-induced dysfunction and death of primary cultured hippocampal neurons through the AKT-BCL-2 signaling pathway through a mechanism that does not involve the Trk receptors and leads to inhibition of caspase-3 activation. |
Databáze: | OpenAIRE |
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