Novel multifunctional nanoliposomes inhibit α-synuclein fibrillization, attenuate microglial activation, and silence the expression of SNCA gene

A. Jebali , M. Rashidi , R. Keikha , K. Daliri , T.F. Outeiro
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Abstract

Introduction

The aim of this study was to compare the effect of five types of PEGlated nanoliposomes (PNLs) on α-synuclein (α-syn) fibrillization, attenuation of microglial activation, and silence of the SNCA gene, which encodes α-syn.

Methods

To evaluate the inhibition of α-syn fibrillization, we used standard in vitro assay based on Thioflavin T (ThT) fluorescence. Next, to evaluate the attenuation of microglial activation, the concentration of TNF-a and IL-6 was quantified by ELISA assay in BV2 microglia cells treated with 100 nM A53T α-syn and PNLs. In order to determine the silencing of the SNCA, real-time PCR and Western blot analysis was used. Finally, the efficacy of PNLs was confirmed in a transgenic mouse model expressing human α-syn.

Results

ThT assay showed both PNL1 and PNL2 significantly inhibited a-syn fibrillization. ELISA test also showed the production of TNF-a and IL-6 was significantly attenuated when microglial cells treated with PNL1 or PNL2. We also found that SNCA gene, at both mRNA and protein levels, was significantly silenced when BV2 microglia cells were treated with PNL1 or PNL2. Importantly, the efficacy of PNL1 and PNL2 was finally confirmed in vivo in a transgenic mouse model.

Conclusions

In conclusion, the novel multifunctional nanoliposomes tested in our study inhibit α-syn fibrillization, attenuate microglial activation, and silence SNCA gene. Our findings suggest the therapeutic potential of PNL1 and PNL2 for treating synucleinopathies.

新型多功能纳米脂质体可抑制α-突触核蛋白纤维化、减轻小胶质细胞活化并抑制 SNCA 基因的表达
引言 本研究的目的是比较五种 PEG 化纳米脂质体(PNLs)对α-突触核蛋白(α-syn)纤维化、小胶质细胞活化减弱以及编码α-syn 的 SNCA 基因沉默的影响。接下来,为了评估小胶质细胞活化的减弱情况,我们用酶联免疫吸附法(ELISA)测定了经 100 nM A53T α-syn 和 PNLs 处理的 BV2 小胶质细胞中 TNF-a 和 IL-6 的浓度。为了确定 SNCA 的沉默情况,采用了实时 PCR 和 Western 印迹分析。最后,在表达人 α-syn 的转基因小鼠模型中证实了 PNLs 的功效。酶联免疫吸附试验(ELISA)也显示,PNL1 和 PNL2 处理小胶质细胞后,TNF-a 和 IL-6 的产生明显减少。我们还发现,用 PNL1 或 PNL2 处理 BV2 小胶质细胞时,SNCA 基因在 mRNA 和蛋白水平上都被明显抑制。重要的是,PNL1 和 PNL2 的疗效最终在转基因小鼠模型中得到了证实。结论总之,我们研究中测试的新型多功能纳米脂质体能抑制 α-syn 纤维化、减轻小胶质细胞活化并沉默 SNCA 基因。我们的研究结果表明,PNL1 和 PNL2 具有治疗突触核蛋白病的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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