Decreased glucose transporters correlate to abnormal hyperphosphorylation of tau in Alzheimer disease

被引:297
作者
Liu, Ying [1 ,2 ]
Liu, Fei [1 ]
Iqbal, Khalid [1 ]
Grundke-Lqbal, Inge [1 ]
Gong, Cheng-Xin [1 ]
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Staten Isl, NY 10314 USA
[2] Wuhan Univ, Renmin Hosp, Dept Cardiol, Wuhan 430060, Peoples R China
关键词
glucose transporters; tau; hyperphosphorylation; Alzheimer disease; O-GleNAcylation; hypoxia-inducible factor;
D O I
10.1016/j.febslet.2007.12.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain glucose uptakelmetabolism is impaired in Alzheimer disease (AD). Here, we report that levels of the two major brain glucose transporters (GLUT1 and GLUT3) responsible for glucose uptake into neurons were decreased in AD brain. This decrease correlated to the decrease in O-GlcNAcylation, to the hyperphosphorylation of tau, and to the density of neurofibrillary tangles in human brains. We also found down-regulation of hypoxia-inducible factor 1, a major regulator of GLUT1 and GLUT3, in AD brain. These studies provide a possible mechanism by which GLUT1 and GLUT3 deficiency could cause impaired brain glucose uptake/metabolism and contribute to neurodegeneration via down-regulation of O-GlcNAcylation and hyperphosphorylation of tau in AD. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:359 / 364
页数:6
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