氯化铁诱导SH-SY5Y细胞氧化应激的作用及其在α-突触核蛋白表达上调中的作用

Mohammed Abba Dige, Emmanuel Paul Okoi
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引用次数: 0

摘要

α-突触核蛋白(SNCA)基因是一种在罕见家族性帕金森病(PD)中发现的致病基因。最近的研究强调了DNA甲基化在家族性和散发性PD发病机制中的作用。SNCA基因的低甲基化与SNCA基因表达的增加有关,并在散发性PD患者死后的大脑中观察到。本研究旨在评估氯化铁(II)对SH-SY5Y细胞模型的影响,其与氧化应激引起的细胞死亡、SNCA基因表达上调和SNCA基因甲基化降低有关。LDH测定结果显示,与对照样品相比,处理过的细胞有显著(p < 0.05)的细胞死亡证据。RT-PCR对SNCA基因进行定量分析,结果显示突变倍数显著增加。1000μM FeCl2处理细胞的倍数变化最大,为6.0,250μM FeCl2处理细胞的倍数变化最小,为1.8。在使用焦磷酸测序的DNA甲基化试验中,细胞用不同浓度的FeCl2处理;生物工程学报,28(3):1-10,2019;文章no.IJBCRR。53099 2的DNA甲基化显著降低(p < 0.05)。在FeCl2浓度为250μM、500μM和750μM时,细胞的平均甲基化水平分别为1.84%、1.40%和1.23%,而浓度为1000 μM时,细胞的平均甲基化水平最低,为1.0%。因此,甲基化的减少与SNCA基因的上调有关,SNCA基因已被报道为帕金森病发病机制的致病因素之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the Effect of Iron (II) Chloride Induced Oxidative Stress in SH-SY5Y Cells and Its Role in Upregulation of α-Synuclein Expression
The α-synuclein (SNCA) gene is a pathogenic gene identified in rare familial Parkinson Disease (PD). Recent studies highlight the role of DNA methylation in the pathogenesis of familial and sporadic PD. Hypomethylation in SNCA gene has been associated with increased SNCA gene expression and was observed in post mortem brains of patients with sporadic PD. This study was aimed at evaluating the effect of iron (II) chloride on SH-SY5Y cell models as pertain to cell death caused by oxidative stress, upregulation of SNCA gene expression and reduced SNCA gene methylation. Result obtained from LDH assay showed significant (p < 0.05) evidence of cell death in treated cells as compared to the control sample. Analysis for SNCA gene quantification using RT-PCR showed significant increases in fold change. Cells treated with 1000μM of FeCl2 showed the highest fold change of 6.0 while cells treated with 250μM had the lowest fold change of 1.8. In DNA methylation assay using pyrosequencing, cells treated with varying concentrations of FeCl2 Original Research Article Dige and Okoi; IJBCRR, 28(3): 1-10, 2019; Article no.IJBCRR.53099 2 showed significant (p < 0.05) decrease in DNA methylation. At 250μM, 500μM and 750μM concentrations of FeCl2, an average mean methylation levels of 1.84%, 1.40% and 1.23% was obtained respectively while cells treated with 1000 μM had the lowest average mean methylation level of 1.0%. Thus, the decrease in methylation is linked to the upregulation of the SNCA gene which has been reported to be among the causative factors in the pathogenesis of Parkinson’s disease.
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