首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Amyloid beta peptide induces cytoplasmic accumulation of amyloid protein precursor via tau protein kinase I/glycogen synthase kinase-3 beta in rat hippocampal neurons.
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Amyloid beta peptide induces cytoplasmic accumulation of amyloid protein precursor via tau protein kinase I/glycogen synthase kinase-3 beta in rat hippocampal neurons.

机译:淀粉样蛋白β肽通过tau蛋白激酶I /糖原合酶激酶-3β在大鼠海马神经元中诱导淀粉样蛋白前体的胞质积累。

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摘要

Exogenous application of synthetic amyloid beta protein (A beta) is known to induce neurotoxic effects in rat hippocampal culture. We report here that A beta (25-35) induces accumulation of amyloid precursor protein (APP) derivatives in the cytoplasm of neurons. At the same time, the level of the secreted form of APP released into the culture medium decreases. Tau protein kinase I/glycogen synthase kinase-3 beta (TPK I/GSK-3 beta) antisense oligonucleotide blocked APP accumulation and prevented neuronal death. These results provide evidence that APP accumulation after A beta treatment is regulated by TPK I/GSK-3 beta. A beta neurotoxicity is probably mediated via phosphorylation of tau by TPK I/GSK-3 beta, resulting in an impairment of axonal transport, and cytoplasmic accumulation of APP.
机译:合成淀粉样β蛋白(A beta)的外源应用已知在大鼠海马培养物中诱导神经毒性作用。我们在这里报告,A beta(25-35)诱导淀粉样前体蛋白(APP)衍生物积累在神经元的细胞质中。同时,释放到培养基中的APP的分泌形式的水平降低。 Tau蛋白激酶I /糖原合酶激酶3 beta(TPK I / GSK-3 beta)反义寡核苷酸可阻止APP积累并防止神经元死亡。这些结果提供了证据,表明A beta处理后APP的积累受TPK I / GSK-3 beta调节。 β神经毒性可能是通过TPK I / GSK-3β磷酸化tau介导的,导致轴突运输受损和APP的胞质积累。

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