Publication: Inhibition of the antioxidant enzyme PRDX1 activity promotes MPP<sup>+</sup>-induced death in differentiated SH-SY5Y cells and may impair its colocalization with eEF1A2
Issued Date
2020-10-01
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18790631
00243205
00243205
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2-s2.0-85089284270
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Mahidol University
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SCOPUS
Bibliographic Citation
Life Sciences. Vol.258, (2020)
Suggested Citation
Wimon Wirakiat, Athinan Prommahom, Permphan Dharmasaroja Inhibition of the antioxidant enzyme PRDX1 activity promotes MPP<sup>+</sup>-induced death in differentiated SH-SY5Y cells and may impair its colocalization with eEF1A2. Life Sciences. Vol.258, (2020). doi:10.1016/j.lfs.2020.118227 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/57671
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Title
Inhibition of the antioxidant enzyme PRDX1 activity promotes MPP<sup>+</sup>-induced death in differentiated SH-SY5Y cells and may impair its colocalization with eEF1A2
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Abstract
© 2020 Elsevier Inc. Aim: eEF1A2 is highly expressed in postmitotic cells and has been reported to interact with the antioxidant enzyme peroxiredoxin 1 (PRDX1). PRDX1 is involved in motor neuron differentiation. Here, we studied the relationship between eEF1A2 and PRDX1 during dopaminergic neuron differentiation, and examined their possible association in an oxidative stress model of Parkinson's disease (PD). Main methods: Expression of eEF1A2 and PRDX1 in SH-SY5Y cells at various durations of retinoic acid (RA) induction was detected using qRT-PCR, Western blotting and immunofluorescence. Neurons of 10-day differentiation were treated with the PRDX1 inhibitor H7, MPP+ and H7 plus MPP+. The cell viability, the amounts of apoptotic nuclei, DHE signals, and the expression of p53, p-Akt and p-mTOR were determined. The colocalization of eEF1A2 and PRDX1 was visualized using confocal microscopy. Key findings: eEF1A2 gradually increased after RA-induced differentiation of SH-SY5Y cells, while PRDX1 protein gradually decreased. MPP+ treatment increased eEF1A2 in both undifferentiated and differentiated neurons; however, PRDX1 appeared to elevate only in mature neurons. The inhibition of the PRDX1 activity with H7 promoted MPP+-induced cell death, as evidenced by decreased cell viability, increased apoptotic nuclei, increased the DHE signal, and increased p53. However, H7 induced the activation of the prosurvival Akt and mTOR in MPP+-treated cells. Besides, a colocalization of eEF1A2 and PRDX1 was evidenced in MPP+-treated neurons. This colocalization was possibly prevented by inhibiting the PRDX1 activity, resulting in aggravated neuronal death. Significance: Our results suggest that the possible association between eEF1A2 and PRDX1 may be a promising target for modifying neuronal death in PD.