国家自然科学基金资助项目(39925012, 39970808, 30100057,30170221),国家重点基础研究发展规划项目(973)(G1999054007)和姜学谊基金资助项目.
This work was supported by grants from The National Natural Sciences Foundation of China (39925012, 39970808, 30100057, 30170221), The Science and Technology Committee of China (G1999054007) and JIANG Xue-Yi foundation.
为探讨急性缺氧对tau蛋白磷酸化的影响,将Wistar大鼠脑片进行不同时间的缺氧培养后,对tau蛋白的磷酸化状态及相关磷酸酯酶的活性和表达进行检测.结果显示,急性缺氧使tau蛋白多个丝氨酸位点磷酸化水平下降,蛋白磷酸酯酶-2A(PP-2A)的活性升高,其催化亚单位表达上调,而蛋白磷酸酯酶-1(PP-1)的活性及催化亚单位表达均无明显改变.该研究结果表明:急性缺氧可能通过蛋白磷酸酯酶-2A的上调而使tau蛋白多个丝氨酸位点发生去磷酸化作用.
To explore the effect of acute hypoxia on tau phosphorylation, rat brain slices were incubated at 37℃ for 30 min or 120 min with or without oxygen supply. Then tau phosphorylation was detected by Western blots. The results showed that significant dephosphorylation of tau at Ser-396/Ser-404, Ser-422 and Ser-199/Ser-202 was induced by acute hypoxia. The activity of protein phosphatase-2A (PP-2A) and the expression of PP-2A catalytic subunit were simultaneously increased. The results suggest that acute hypoxia induces dephosphorylation of tau and the up-regulation of PP-2A may be at least one of the underlying mechanisms.
刘蓉,王小川,黄尧,何志松,楮淑娟,汤芸,田青,王建枝.急性缺氧和急性低糖对脑片tau蛋白磷酸化的影响[J].生物化学与生物物理进展,2004,31(5):402-408
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