Guan Zhi-zhong, Shan Ke-ren, Xiu Jin, Long Yi-guo
Key Laboratory of Molecular Biology, Department of Pathology, Guiyang Medical College, Guizhou 550004, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2005 Jan;39(1):26-9.
To investigate the influence of fluorosis on nicotinic acetylcholine receptors (nAChRs) in protein and gene levels in SH-SY5Y cells and the mechanism of the receptor modification.
SH-SY5Y cells, a human neuroblastoma cell line, were incubated with different concentrations of fluoride or with antioxidant for 48 hours. The functions of cells were measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) method, and protein oxidation detected by carbonyl content; the alpha3 and alpha7 nAChR subunits in protein level were measured by Western blotting and in mRNA level by RT-polymerase chain reaction (RT-PCR).
In high-dose group as compared to the control, the decreased MTT (49%), increased protein oxidation (72%), and lower expression of alpha3 (51%) and alpha7 (47%) nAChR subunit proteins were obviously observed in SH-SY5Y cells. There were no changes in expression of nAChR subunit mRNAs between the cells treated with fluoride and those un-treated in controls. Prior treatment with antioxidant resulted in preventing the decrease of nAChR protein in cells exposed to the high doses of fluoride.
Fluorosis should result in damage of cells and the declined expression of nAChRs in protein levels, but no influences on gene expression of the receptors in human neuroblastoma neurons. The decreased nAChR proteins might be involved in the mechanism of oxidative stress induced by fluorosis.
研究氟中毒对人神经母细胞瘤SH-SY5Y细胞中烟碱型乙酰胆碱受体(nAChRs)蛋白和基因水平的影响以及受体修饰的机制。
将人神经母细胞瘤细胞系SH-SY5Y细胞与不同浓度的氟或抗氧化剂孵育48小时。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法检测细胞功能,通过羰基含量检测蛋白质氧化;采用蛋白质印迹法检测α3和α7 nAChR亚基的蛋白水平,采用逆转录聚合酶链反应(RT-PCR)检测mRNA水平。
与对照组相比,高剂量组SH-SY5Y细胞中MTT明显降低(49%),蛋白质氧化增加(72%),α3(51%)和α7(47%)nAChR亚基蛋白表达明显降低。氟处理细胞与未处理的对照细胞之间nAChR亚基mRNA表达无变化。预先用抗氧化剂处理可防止高剂量氟暴露细胞中nAChR蛋白的减少。
氟中毒可导致细胞损伤和nAChRs蛋白水平表达下降,但对人神经母细胞瘤神经元中受体的基因表达无影响。nAChR蛋白减少可能参与了氟中毒诱导的氧化应激机制。