期刊文献+

麦芽酚铝对大鼠肾上腺嗜铬细胞瘤细胞β-淀粉样蛋白42蛋白表达的影响及其作用机制 被引量:1

Effect of aluminum-maltolate on the expression of Aβ42 proteins in PC12 of rats cells and its mechanism
原文传递
导出
摘要 目的探讨铝对大鼠肾上腺嗜铬细胞瘤(PC12)细胞β-淀粉样蛋白(Aβ)42表达的影响及其作用机制。方法将处于对数生长期的PC12细胞分别暴露于含麦芽酚铝终浓度为0(对照)、50、100、200和400μmol/L的完全培养基染毒12、24、48 h。采用CCK-8法测定细胞活性,采用酶联免疫吸附(ELISA)测定法测定PS1、Aβ42蛋白的含量。结果与对照组比较,200、400μmol/L麦芽酚铝染毒12 h时及各浓度麦芽酚铝染毒24 h、48 h时PC12细胞的存活率均较低,差异有统计学意义(P<0.05);且随着麦芽酚铝染毒浓度的升高,不同染毒时间PC12细胞的存活率均呈逐渐降低的趋势。与对照组比较,400μmol/L麦芽酚铝染毒12 h时及200、400μmol/L麦芽酚铝染毒24 h、48 h时PC12细胞PS1蛋白的含量均增加,差异有统计学意义(P<0.05)。与对照组比较,400μmol/L麦芽酚铝染毒12 h时及200、400μmol/L麦芽酚铝染毒24 h时以及100、200、400μmol/L麦芽酚铝染毒48 h时PC12细胞Aβ42蛋白的含量均增加,差异有统计学意义(P<0.05)。结论γ-分泌酶表达增加可能是铝致PC12细胞Aβ42蛋白含量增多的重要原因之一。 Objective To explore the effect of aluminum on the expression of β-amyloid protein (Aβ) 42 in rats' pheochromocytoma cells(PC12 cells) and its mechanism. Methods The PC12 cells in logarithmic growth phase were incubated in culture media with aluminum-maltolate[Al(mal)3] at final concentration of 0,50,100,200, and 400μmol/L for 12 h, 24 h and 48 h,respectively. The cell counting kit-8 was used to detect cell viability of PC12 cells,and the protein expressions of presenilin I(PS1) and Aβ42 was detected by enzyme-linked immunosorbent assay(ELISA). Results The cell vitality of PC12 cells incubated by 200,400 μmol/L Al(mal)3 for 12 h,or incubated by 50,100,200,and 400 μmol/L Al(mal)3 for 24 h,48 h were significantly decreased compared with the control group (P〈0.05),with statistical significance. The protein expression of PS1 in PC12 ceils treated with 400 μmol/L Al(mal)3 for 12 h or treated with 200,400 μmol/L Al(mal)3 for 24 h,48 h were increased significantly compared with those of control groups (P〈0.05) , with statistical significance. The protein expression of Aβ42 in these PC12 ceils treated with 400 μmol/L Al(mal)3 for 12 h,200,400 μmol/L Al(mal)3 for 24 h,or 100,200,and 400 μmol/L Al(mal)3 for 48 h,were increased significantly compared with those of control group(P〈0.05), with statistical significance. Conclusion The increased expression of γ-seeretase may be one of the reasons for the increased protein expression of Aβ42 in PC12 cells induced by aluminum.
出处 《环境与健康杂志》 CAS 北大核心 2017年第8期659-661,共3页 Journal of Environment and Health
基金 国家自然科学基金(30972512) 山西省自然科学基金(2013011052-1) 山西医科大学博士启动基金(B03201209)
关键词 PC12细胞 早老素1 Β-淀粉样蛋白 Aluminum PC 12 cells Presenilin 1 (PS 1) β-amyloid protein
  • 相关文献

参考文献3

二级参考文献22

  • 1任振华,李光武.铅对小鼠学习记忆及自主活动的影响[J].环境与健康杂志,2006,23(3):237-239. 被引量:14
  • 2Selkoe DJ. Alzheimer disease: mechanistic understanding predicts novel therapies(J]. Ann Intern Med, 2004,140: 627-638.
  • 3Zhang YW, Thompson R,Zhang H, et al. APP processing in Alzheimer's disease [J]. Mol Brain, 2011,4: 3.
  • 4Wang C, Yang XM, Zhuo YY, et al. The phosphodiesterase--4 inhibitor rolipram reverses Abeta -induced cognitive impairment and neuroinflammatory and apoptotic responses in rats [J]. IntJNeuropsychopharmacol, 2012,15 : 1-18.
  • 5Gilbert ME, Lasley SM. Developmental lead (Pb) exposure reduces the ability of the NMDA antagonist MK-801 to suppress long-term potentiation (LTP) in the rat dentate gyrus,in vivo J]. Neurotoxicol Teratol, 2007,29: 385-393.
  • 6Gu H, Wei X, Mormot AD, et al. Lead exposure increases levels of beta-amyloid in the brain and CSF and inhibits LRP1 expression in APP transgenic mice[J]. Neuroaci Lett, 2011,490: 16-20.
  • 7Bihaqi SW, Huang H, WuJ, et al. Infant exposure to lead (Pb) and epigenetic modifications in the aging primate brain:implications for Alzheimer's disease[J].JAlzheimers Dis, 2011, 27: 819-833.
  • 8Sugiyama T, Utsunomiya K, Ota H, et al. Comparative study of cerebral blood flow in patients with normal-tension glaucoma and control subjectsJ]. AmJOphthalmol,2006,141 : 394-396.
  • 9Bihaqi SW, Zawia NH. Alzheimer's disease biomarkers and epigenetic intermediates following exposure to Pb in vitroJ]. Curr Alzheimer Res, 2012,9 : 555-562.
  • 10Sarajarvi T, Haapasalo A, ViswanathanJ, et al. Down-regulation of seladin-1 increases BACE1 levels and activity through enhanced GGA3 depletion during apoptosis J].JBiol Chem, 2009,284:34433-34443.

共引文献8

同被引文献5

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部