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人类神经发育与退行性变中的汇聚分子途径。

Converging molecular pathways in human neural development and degeneration.

机构信息

Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, Sahlgrenska Academy at University of Gothenburg, Göteborg/Mölndal, Sweden.

出版信息

Neurosci Res. 2010 Mar;66(3):330-2. doi: 10.1016/j.neures.2009.11.012. Epub 2009 Dec 2.

Abstract

Animal studies suggest that phosphorylation of microtubule-associated protein tau is a physiological way of destabilizing axons in the developing brain, promoting synaptic plasticity, while in the adult human brain tau phosphorylation is a specific sign of Alzheimer's disease. We here show, for the first time, that newborn human infants have extremely high levels of phosphorylated tau in their cerebrospinal fluid, and that these levels decrease during the first years of life. Tau phosphorylation in Alzheimer's disease may be a physiological response to Alzheimer-associated synaptotoxicity.

摘要

动物研究表明,微管相关蛋白 tau 的磷酸化是一种在发育中的大脑中不稳定轴突、促进突触可塑性的生理方式,而在成年人大脑中 tau 磷酸化是阿尔茨海默病的一个特定标志。我们在这里首次表明,新生人类婴儿的脑脊液中存在极高水平的磷酸化 tau,并且这些水平在生命的头几年中下降。阿尔茨海默病中的 tau 磷酸化可能是对与阿尔茨海默病相关的突触毒性的一种生理反应。

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