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机构地区:[1]青岛大学医学院生物化学与分子生物学教研室,山东青岛266021
出 处:《山东医药》2016年第45期23-26,共4页Shandong Medical Journal
基 金:国家自然科学基金项目(81472542)
摘 要:目的探讨2,3-吲哚醌对神经母细胞瘤细胞SH-SY5Y侵袭转移的影响及机制。方法体外培养SHSY5Y细胞,用不同浓度(50、100、200、300μmol/L)的2,3-吲哚醌处理细胞48 h,并设不加药物处理的细胞作为对照组,CCK-8法检测细胞活性,筛选合适的2,3-吲哚醌浓度;用吖啶橙染色法检测对照组和200μmol/L 2,3-吲哚醌处理组(加药组)的自噬溶酶体细胞数量;将细胞分别用50、100、200、300μmol/L 2,3-吲哚醌处理(加药组),并设空白对照,48 h后用Western blotting法检测自噬标志性蛋白LC3-Ⅱ的表达水平,Transwell小室试验检测细胞的侵袭能力,划痕试验检测细胞迁移能力。结果与对照组相比,随着2,3-吲哚醌浓度的升高,细胞A450值降低,药物对细胞的抑制率升高(P<0.05或<0.01)。吖啶橙染色结果显示,与对照组相比,加药组产生自噬溶酶体的细胞数增多(P<0.01)。Western blotting结果显示,与空白对照比较,随着药物浓度增加,加药组LC3-Ⅱ表达增多(P<0.05或<0.01);Transwell小室试验和划痕试验表明,随着2,3-吲哚醌浓度的增加,SH-SY5Y细胞侵袭转移能力逐渐减弱(P均<0.05)。结论 2,3-吲哚醌可能通过诱导神经母细胞瘤细胞SH-SY5Y自噬,从而抑制其侵袭转移。Objective To investigate the effect of 2,3-isatin on the invasion and metastasis of neuroblastoma SHSY5 Y cells and the mechanism. Methods SH-SY5 Y cells cultured in vitro were treated for 48 h with different concentrations of 2,3-isatin( 25,50,100,200 and 300 μmol/L). The cell viability was measured by CCK-8. The number of cells with autolysosome in the control group and 200 μmol/L isatin-treated group was detected by acridine orange staining fluorescence. The expression of LC3 Ⅱ,a marker protein for autophagy was examined by Western blotting. The invasion of SH-SY5 Y cells was tested by Transwell assay and the motile ability was detected by Scratch test. Results Compared with the control group,the A450 value decreased and the inhibition rate increased when the concentration of 2,3-isatin was higher than 100 μmol/L( P〈0. 05 or P〈0. 01). AO staining showed that the number of autolysosomes increased in the200 μmol/L 2,3-isatin treatment group as compared with that of the control group( P〈0. 01). Western blotting showed that the expression of LC3-Ⅱincreased with the increasing drug concentration( P〈0. 05). Transwell assay and Scratch test showed that the invasion and motile abilities of SH-SY5 Y cells diminished with the increasing concentration of 2,3-isatin( all P〈0. 05). Conclusion 2,3-isatin may inhibit the invasion and metastasis of SH-SY5 Y cells by inducing the autophagy.
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