中国生化药物杂志2017,Issue(7) :23-24,28.DOI:10.3969/j.issn.1005-1678.2017.07.007

A2AR活化在脑创伤后tau蛋白过度磷酸化中的作用和机制分析

Analysis of the role and mechanism of A2AR activation in tau hyperphosphorylation after brain injury

张克利 郭志刚
中国生化药物杂志2017,Issue(7) :23-24,28.DOI:10.3969/j.issn.1005-1678.2017.07.007

A2AR活化在脑创伤后tau蛋白过度磷酸化中的作用和机制分析

Analysis of the role and mechanism of A2AR activation in tau hyperphosphorylation after brain injury

张克利 1郭志刚1
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作者信息

  • 1. 天津市宝坻区人民医院,天津医科大学宝坻临床学院 神经外科,天津 301800
  • 折叠

摘要

目的 研究A2AR活化在脑创伤后tau蛋白过度磷酸化中的作用和机制.方法 选择无特定病原体级的SD大鼠、SH-SY5Y进行培养,大鼠原代海马神经元分别加CGS21680溶液和DMSO,SH-SY5Y的观察组分别加CGS21680溶液,及sb216763、H-89,或只加ZM241385,对照组加DMSO,对比各组tau蛋白过度磷酸化情况.结果 大鼠原代海马神经元tau蛋白磷酸化水平明显高于对照组,差异有统计学意义(P<0.05);SH-SY5Y细胞中,观察1组tau蛋白磷酸化水平明显升高,与其他组相比,差异有统计学意义(P<0.05);观察2组和3组tau蛋白磷酸化水平明显高于对照组,差异有统计学意义(P<0.05);观察4组和5组tau蛋白磷酸化水平与对照组比较,差异无统计学意义.结论 脑创伤后A2AR活化能够激活激酶A和GSK-3β,从而导致tau蛋白过度磷酸化.

Abstract

Objective To study the role and mechanism of A2AR activation in tau hyperphosphorylation after brain injury.Methods SD rats were cultured with no specific pathogen level.SH-SY5Y was cultured.The rats were treated with CGS21680 solution and DMSO and SH-SY5Y respectively.The CGS21680 solution and sb216763, H-89, or Only add ZM241385, the control group plus DMSO, compared with each group tau hyperphosphorylation.Results The phosphorylation level of tau protein in SH-SY5Y cells was significantly higher than that in the control group (P<0.05).The phosphorylation level of tau protein in the primary hippocampal neurons of rats was significantly higher than that of the control group (P<0.05).The levels of tau protein phosphorylation in group 2 and group 3 were significantly higher than those in control group (P<0.05).The expression of tau in group 4 and group 5 was statistically significant (P<0.05)There was no significant difference in phosphorylation level between the two groups.Conclusion A2AR activation can activate kinase A and GSK-3β after brain injury, leading to tau hyperphosphorylation.

关键词

A2AR/脑创伤/tau蛋白过度磷酸化/机制

Key words

A2AR/brain trauma/tau hyperphosphorylation/mechanism

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出版年

2017
中国生化药物杂志
南京生物化学制药研究所,全国生化制药情报中心站,中国生化制药工业协会,中国药品生物制品检定所

中国生化药物杂志

ISSN:1005-1678
参考文献量8
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