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首页> 外文期刊>Cellular and Molecular Neurobiology >Hyperphosphorylation and accumulation of neurofilament proteins in transgenic mice with Alzheimer presenilin 1 mutation.
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Hyperphosphorylation and accumulation of neurofilament proteins in transgenic mice with Alzheimer presenilin 1 mutation.

机译:阿尔茨海默氏早老素1突变的转基因小鼠中神经丝蛋白的过度磷酸化和积累。

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摘要

Neurofilaments (NFs) are hyperphosphorylated and accumulate in Alzheimer's disease (AD) brains. In this study, employing the transgenic mouse model, we explored the effect of presenilin 1 (PS-1) mutation on the phosphorylation and distribution of NFs. Western blot analysis showed that there was a significant increase in the phosphorylation of NF-H and NF-M subunits with a concomitant increase in phosphorylated c-Jun N-terminal protein kinase 1/2 (JNK1/2) mitogen-activated protein kinase (MAPK) in hippocampus of PS-1 transgenic mice compared to that of wild-type littermates. Immunohistochemical analysis revealed that phosphorylated NFs accumulated throughout the hippocampal neurons of the transgenic mice. These findings suggest that PS-1 mutation may induce hyperphosphorylation and accumulation of NFs via a JNK1/2-involved mechanism.
机译:神经丝(NFs)过度磷酸化,并在阿尔茨海默氏病(AD)大脑中积累。在这项研究中,采用转基因小鼠模型,我们探索了早老素1(PS-1)突变对NFs磷酸化和分布的影响。 Western印迹分析表明NF-H和NF-M亚基的磷酸化显着增加,而磷酸化的c-Jun N端蛋白激酶1/2(JNK1 / 2)丝裂原激活的蛋白激酶(与野生型同窝仔相比,PS-1转基因小鼠海马中的MAPK)。免疫组织化学分析表明,磷酸化的NFs累积在转基因小鼠的整个海马神经元中。这些发现表明PS-1突变可能通过JNK1 / 2参与的机制诱导NF的过度磷酸化和积累。

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