首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Rapid dephosphorylation of tau in heat-shocked fetal rat cerebral explants: prevention and hyperphosphorylation by inhibitors of protein phosphatases PP1 and PP2A.
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Rapid dephosphorylation of tau in heat-shocked fetal rat cerebral explants: prevention and hyperphosphorylation by inhibitors of protein phosphatases PP1 and PP2A.

机译:热休克胎儿大鼠脑外植体中tau的快速去磷酸化:蛋白磷酸酶PP1和PP2A抑制剂的预防和过度磷酸化。

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We heat shocked 21- and 35-day-old fetal rat cerebral explants at 45 degrees C for 18 min and performed immunocytochemistry and immunoblot analysis of sodium dodecyl sulfate extracts using the monoclonal anti-tau antibodies Tau-1, Tau-5, Tau-46, and PHF-1 and the peroxidase-antiperoxidase technique or 125I-labeled protein A. Tau-1 and PHF-1 recognize nonphosphorylated and phosphorylated epitopes, respectively, and both Tau-5 and Tau-46 recognize phosphate-independent epitopes. tau immunoreactivity was confined to neurons and increased in heat-shocked perikarya but not axons. At 0 h after heat shocking, there was dephosphorylation of tau exemplified by (1) faster migration of tau isoforms with resultant loss or attenuation of the 60- and 52-kDa tau isoforms recognized by all four anti-tau antibodies and concomitant accentuation of the fastest moving 50-kDa tau isoform recognized by Tau-1, Tau-5, and Tau-46; and (2) significant increase in the nonphosphorylated Tau-1 epitope with resultant decreases in the ratio of total (phosphorylated plus nonphosphorylated) tau to nonphosphorylated tau and the difference of total tau minus nonphosphorylated tau. tau was phosphorylated back to the control level by 12 h and remained so at 24 and 48 h after heat shocking. Treatment of explants with cycloheximide, a protein synthesis inhibitor, did not prevent the heat shocking-induced dephosphorylation of tau. Treatment of explants with the inhibitors of protein phosphatases PP1 and PP2A, okadaic acid or calyculin A, produced hyperphosphorylated tau polypeptides, prevented the heat shocking-induced dephosphorylation of tau, and intensified the immunoreactivity of the neurofilament subunit H with the only antiphosphoneurofilament antibody that reacts with intraneuronal neurofibrillary tangles. In 35-day-old explants, in addition to the three 50-, 52-, and 60-kDa tau isoforms seen in 21-day-old explants, a 66-kDa tau polypeptide was also present.
机译:我们在45摄氏度下对21天和35天的胎鼠脑外植体进行电击处理18分钟,并使用单克隆抗tau抗体Tau-1,Tau-5,Tau-进行十二烷基硫酸钠提取物的免疫细胞化学和免疫印迹分析。 Tau-1和PHF-1分别识别非磷酸化和磷酸化的抗原决定簇,Tau-5和Tau-46识别不依赖磷酸酯的抗原决定簇,分别使用图46和PHF-1和过氧化物酶-抗过氧化物酶技术或125I标记的蛋白A。 tau免疫反应性仅限于神经元,在热激周膜细胞中增加,但在轴突中则没有。在热休克后0小时,tau发生了磷酸化,其表现为(1)tau异构体的迁移更快,导致所有四种抗tau抗体识别的60 kDa和52 kDa tau异构体的损失或减弱,并伴随着tau异构体的增强。 Tau-1,Tau-5和Tau-46识别的移动最快的50 kDa tau异构体; (2)非磷酸化Tau-1表位的显着增加,导致总(磷酸化与非磷酸化)tau与非磷酸化tau的比率以及总tau减去非磷酸化tau的差值降低。 tau在12 h之前被磷酸化回到对照水平,并在热冲击后的24和48 h保持磷酸化。用蛋白质合成抑制剂环己酰亚胺处理外植体并不能防止热激诱导的tau磷酸化。用蛋白磷酸酶PP1和PP2A,冈田酸或calyculin A抑制剂处理外植体,产生高磷酸化的tau多肽,防止热激诱导的tau磷酸化,并增强神经丝亚基H与唯一反应的抗磷酸化纤维丝抗体的免疫反应性与神经内神经原纤维缠结。在35天大的外植体中,除了在21天大的外植体中看到的三个50、52和60 kDa tau异构体之外,还存在一个66 kDa tau多肽。

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