ApoE4 disrupts sterol and sphingolipid metabolism in Alzheimer's but not normal brain

被引:116
作者
Bandaru, Veera Venkata Ratnam [1 ]
Troncoso, Juan [1 ,2 ]
Wheeler, David [1 ]
Pletnikova, Olga [2 ]
Wang, Jessica [1 ]
Conant, Kathy [1 ]
Haughey, Norman J. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21287 USA
关键词
Alzheimer's disease; Apolipoprotein; ApoE; ApoE4; Sterol; Cholesterol; Sphingomeylin; Ceramide; Sphingolipid; HUMAN APOLIPOPROTEIN-E; CEREBROSPINAL-FLUID; BETA-SECRETASE; CHOLESTEROL; CERAMIDE; RECEPTOR; DENSITY; DISEASE; E4; NEURONS;
D O I
10.1016/j.neurobiolaging.2007.07.024
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The epsilon 4 allele of ApoE is associated with an earlier onset and faster progression of Alzheimer's disease in patients with the familial form of this neurodegenerative condition. Although ApoE4 has been repeatedly associated with altered sphingomyelin and cholesterol levels in tissue culture and rodent models, there has not been a direct quantification of sphingomyelin or sterol levels in the brains of patients with different forms of ApoE. We measured the sphingolipid and sterol content of human brain tissues and found no evidence of perturbed sterol or sphingolipid biochemistry in the brains of individuals expressing ApoE4 who did not have a preexisting neurodegenerative condition. Nevertheless, ApoE4 was associated with gross abnormalities in the sterol and sphingolipid content of numerous brain regions in patients with Alzheimer's diseaase. The findings suggest that ApoE4 may not by itself alter sterol or sphingolipid metabolism in the brain under normal conditions, but that other neuropathologic changes of Alzheimer's are required to unmask the effect of ApoE4, and to perturb sterol and sphingolipid biochemistry. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:591 / 599
页数:9
相关论文
共 44 条
[1]   Neuronal membrane cholesterol loss enhances amyloid pepticle generation [J].
Abad-Rodriguez, J ;
Ledesma, MD ;
Craessaerts, K ;
Perga, S ;
Medina, M ;
Delacourte, A ;
Dingwall, C ;
De Strooper, B ;
Dotti, CG .
JOURNAL OF CELL BIOLOGY, 2004, 167 (05) :953-960
[2]  
Bodovitz S, 1996, J BIOL CHEM, V271, P4436
[3]  
Bohnet K, 1996, J LIPID RES, V37, P1316
[4]  
Brann AB, 1999, J NEUROSCI, V19, P8199
[5]   Apolipoprotein E isoform mediated regulation of nitric oxide release [J].
Brown, CM ;
Wright, E ;
Colton, CA ;
Sullivan, PM ;
Laskowitz, DT ;
Vitek, MP .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1071-1075
[6]   Activation of Fas receptor is required for the increased formation of the disialoganglioside GD3 in cultured cerebellar granule cells committed to apoptotic death [J].
Castiglione, M ;
Spinsanti, P ;
Iacovelli, L ;
Lenti, L ;
Martini, F ;
Gradini, R ;
Gerevini, VD ;
Caricasole, A ;
Caruso, A ;
De Maria, R ;
Nicoletti, F ;
Melchiorri, D .
NEUROSCIENCE, 2004, 126 (04) :889-898
[7]   Apolipoprotein-E allele-specific regulation of nitric oxide production [J].
Colton, CA ;
Brown, CM ;
Czapiga, M ;
Vitek, MP .
NITRIC OXIDE: NOVEL ACTIONS, DELETERIOUS EFFECTS AND CLINICAL POTENTIAL, 2002, 962 :212-225
[8]   Exclusively targeting β-secretase to lipid rafts by GPI-anchor addition up-regulates β-site processing of the amyloid precursor protein [J].
Cordy, JM ;
Hussain, I ;
Dingwall, C ;
Hooper, NM ;
Turner, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (20) :11735-11740
[9]   Dysregulation of sphingolipid and sterol metabolism by ApoE4 in HIV dementia [J].
Cutler, RG ;
Haughey, NJ ;
Tammara, A ;
McArthur, JC ;
Nath, A ;
Reid, R ;
Vargas, DL ;
Pardo, CA ;
Mattson, MP .
NEUROLOGY, 2004, 63 (04) :626-630
[10]   Involvement of oxidative stress-induced abnormalities in ceramide and cholesterol metabolism in brain aging and Alzheimer's disease [J].
Cutler, RG ;
Kelly, J ;
Storie, K ;
Pedersen, WA ;
Tammara, A ;
Hatanpaa, K ;
Troncoso, JC ;
Mattson, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (07) :2070-2075