Zhao Liang, Xiao Yan, Wang Xiao-Liang, Pei Jinjing, Guan Zhi-Zhong
Department of Pathology at the Affiliated Hospital, Guizhou Medical University, Guiyang 550004, Guizhou, PR China.
The Key Laboratory of Medical Molecular Biology, Guizhou Medical University, Guiyang 550004, Guizhou, PR China.
Exp Biol Med (Maywood). 2016 Oct;241(16):1825-33. doi: 10.1177/1535370216650759. Epub 2016 May 13.
The aim of the study was to investigate the influence of hyperphosphorylation of tau induced by okadaic acid on the expression of nicotinic acetylcholine receptors and the neurotoxicity of β-amyloid peptide. Primary cultures of neurons isolated from the hippocampus of the brains of neonatal rats were exposed to okadaic acid or/and Aβ1-42 Tau phosphorylated at Ser404 and Ser202, and the protein expressions of α7, α4 and α3 nAChR subunits were quantified by Western blotting, and their corresponding mRNAs by real-time PCR. Superoxide dismutase activity was assayed biochemically and malondialdehyde by thiobarbituric acid-reactive substance. As compared to controls, phosphorylations of tau at Ser404 and Ser202 in the neurons were elevated by exposure to 20 nM okadaic acid for 48 h but not by 1 or 2 µM Aβ1-42 Treatment with 20 nM okadaic acid or 1 µM Aβ1-42 for 48 h resulted in the reduced α7, α4 and α3 proteins, and α4 and α3 mRNAs, as well as the decreased activity of superoxide dismutase and the increased malondialdehyde. Okadaic acid and Aβ1-42 together caused more pronounced changes in the expressions of α7 and α4, superoxide dismutase activity and lipid peroxidation than either alone. When pre-treatment with vitamin E or lovastatin, the neurotoxicity induced by okadaic acid was significantly attenuated. These findings indicate that hyperphosphorylation of tau induced by okadaic acid inhibits the expression of nicotinic acetylcholine receptors at both the protein and mRNA levels, as well as enhances the neurotoxicity of β-amyloid peptide.
本研究旨在探讨冈田酸诱导的tau蛋白过度磷酸化对烟碱型乙酰胆碱受体表达及β-淀粉样肽神经毒性的影响。将新生大鼠海马神经元原代培养物暴露于冈田酸或/和Aβ1-42,检测Ser404和Ser202位点磷酸化的Tau蛋白,采用蛋白质免疫印迹法定量α7、α4和α3 nAChR亚基的蛋白表达,实时荧光定量PCR法检测其相应mRNA。采用生化方法检测超氧化物歧化酶活性,硫代巴比妥酸反应物质法检测丙二醛含量。与对照组相比,暴露于20 nM冈田酸48 h可使神经元中Ser404和Ser202位点的tau蛋白磷酸化水平升高,而1或2 μM Aβ1-42则无此作用。用20 nM冈田酸或1 μM Aβ1-42处理48 h可导致α7、α4和α3蛋白及α4和α3 mRNA表达降低,超氧化物歧化酶活性降低,丙二醛含量增加。冈田酸和Aβ1-42共同作用比单独作用更显著地改变α7和α4的表达、超氧化物歧化酶活性和脂质过氧化。预先用维生素E或洛伐他汀处理后,冈田酸诱导的神经毒性明显减弱。这些结果表明,冈田酸诱导的tau蛋白过度磷酸化在蛋白质和mRNA水平上抑制烟碱型乙酰胆碱受体的表达,并增强β-淀粉样肽的神经毒性。