Molecular and Clinical Pharmacology, ICBM, Faculty of Medicine, University of Chile, Santiago, Chile.
Neurotox Res. 2017 Oct;32(3):362-367. doi: 10.1007/s12640-017-9747-4. Epub 2017 May 6.
Alpha-synuclein (SNCA) oligomers have been reported to inhibit autophagy. Aminochrome-induced SNCA oligomers are neurotoxic, but the flavoenzyme DT-diaphorase prevents both their formation and their neurotoxicity. However, the possible protective role of DT-diaphorase against autophagy impairment by aminochrome-induced SNCA oligomers remains unclear. To test this idea, we used the cell line RCSN-3NQ7SNCA, with constitutive expression of a siRNA against DT-diaphorase and overexpression SNCA, and RCSN-3 as control cells. A significant increase in LC3-II expression was observed in RCSN-3 cells treated with 20 μM aminochrome and 10 μM rapamycin followed by a decrease in cell death compared to RCSN-3 cells incubated with 20 μM aminochrome alone. The incubation of RCSN-3NQ7SNCA cells with 20 μM aminochrome and 10 μM rapamycin does not change the expression of LC3-II in comparison with RCSN-3NQ7SNCA cells incubated with 20 μM aminochrome alone. The incubation of both cell lines preincubated with 100 nM bafilomycin and 20 μM aminochrome increases the level of LC3-II. Under the same conditions, cell death increases in both cell lines in comparison with cells incubated with 20 μM aminochrome. These results support the protective role of DT-diaphorase against SNCA oligomers-induced autophagy inhibition.
α-突触核蛋白(SNCA)寡聚体已被报道能抑制自噬。氨基chrome 诱导的 SNCA 寡聚体具有神经毒性,但黄素酶 DT-二氢醌氧化还原酶可防止其形成和神经毒性。然而,DT-二氢醌氧化还原酶对氨基chrome 诱导的 SNCA 寡聚体引起的自噬损伤的可能保护作用尚不清楚。为了验证这一观点,我们使用了 RCSN-3NQ7SNCA 细胞系,该细胞系稳定表达针对 DT-二氢醌氧化还原酶的 siRNA 和过量表达的 SNCA,并用 RCSN-3 作为对照细胞。与单独用 20μM 氨基chrome 孵育的 RCSN-3 细胞相比,用 20μM 氨基chrome 和 10μM 雷帕霉素处理的 RCSN-3 细胞中 LC3-II 的表达显著增加,细胞死亡减少。与单独用 20μM 氨基chrome 孵育的 RCSN-3NQ7SNCA 细胞相比,用 20μM 氨基chrome 和 10μM 雷帕霉素孵育的 RCSN-3NQ7SNCA 细胞中 LC3-II 的表达没有变化。与单独用 20μM 氨基chrome 孵育的细胞相比,两种细胞系在预先用 100nM 巴弗洛霉素和 20μM 氨基chrome 孵育后,LC3-II 的水平均增加。在相同条件下,与用 20μM 氨基chrome 孵育的细胞相比,两种细胞系的细胞死亡均增加。这些结果支持 DT-二氢醌氧化还原酶对 SNCA 寡聚体诱导的自噬抑制的保护作用。