Front Cell Neurosci. 2015 May 28;9:209. doi: 10.3389/fncel.2015.00209. eCollection 2015.
Lithium protects against paraquat neurotoxicity by NRF2 activation and miR-34a inhibition in SH-SY5Y cells.
Frontiers in cellular neuroscience
Begum Alural, Aysegul Ozerdem, Jens Allmer, Kursad Genc, Sermin Genc
Affiliations
Affiliations
- Izmir Biomedicine and Genome Center, Dokuz Eylul University Izmir, Turkey ; Department of Neuroscience, Health Science Institute, Dokuz Eylul University Izmir, Turkey.
- Department of Neuroscience, Health Science Institute, Dokuz Eylul University Izmir, Turkey ; Department of Psychiatry, School of Medicine, Dokuz Eylul University Izmir, Turkey.
- Department of Molecular Biology and Genetics, Izmir Institute of Technology Urla, Turkey.
- Department of Neuroscience, Health Science Institute, Dokuz Eylul University Izmir, Turkey.
PMID: 26074776
PMCID: PMC4446540 DOI: 10.3389/fncel.2015.00209
Abstract
Lithium is a mood stabilizing agent commonly used for the treatment of bipolar disorder. Here, we investigated the potential neuroprotective effect of lithium against paraquat toxicity and its underlying mechanisms in vitro. SH-SY5Y human neuroblastoma cells were treated with paraquat (PQ) 0.5 mM concentration after lithium pretreatment to test lithium's capability in preventing cell toxicity. Cell death was evaluated by LDH, WST-8, and tryphan blue assays. Apoptosis was analyzed using DNA fragmentation, Annexin V immunostaining, Sub G1 cell cycle analysis, and caspase-3 activity assays. BCL2, BAX, and NRF2 protein expression were evaluated by Western-blotting and the BDNF protein level was determined with ELISA. mRNA levels of BCL2, BAX, BDNF, and NRF2 target genes (HO-1, GCS, NQO1), as well as miR-34a expression were analyzed by qPCR assay. Functional experiments were done via transfection with NRF2 siRNA and miR-34a mimic. Lithium treatment prevented paraquat induced cell death and apoptosis. Lithium treated cells showed increased anti-apoptotic protein BCL2 and decreased pro-apoptotic protein BAX expression. Lithium exerted a neurotrophic effect by increasing BDNF protein expression. It also diminished reactive oxygen species production and activated the redox sensitive transcription factor NRF2 and increased its target genes expression. Knockdown of NRF2 abolished neuroprotective, anti-apoptotic, and anti-oxidant effects of lithium. Furthermore, lithium significantly decreased both basal and PQ-induced expression of miR-34a. Transfection of miR-34a specific mimic reversed neuroprotective, anti-apoptotic, and anti-oxidant effects of lithium against PQ-toxicity. Our results revealed two novel mechanisms of lithium neuroprotection, namely NRF2 activation and miR-34a suppression.
Keywords: NRF2; Parkinson's disease; bipolar disorder; lithium; miR-34a
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