Cerebral amyloid angiopathy plays a direct role in the pathogenesis of Alzheimer's disease Pro-CAA position statement

被引:138
作者
Nicoll, JAR
Yamada, M
Frackowiak, J
Mazur-Kolecka, B
Weller, RO
机构
[1] Univ Southampton, Southampton Gen Hosp, Southampton SO16 6YD, Hants, England
[2] Kanazawa Univ, Grad Sch Med, Dept Neurol & Neurobiol Aging, Kanazawa, Ishikawa 920, Japan
[3] New York State Inst Basic Res Dev Disabil, Staten Isl, NY 10314 USA
关键词
Alzheimer's disease; amyloid beta-protein; cerebrovascular disease; cerebral amyloid angiopathy; lipid transport; apolipoprotein E; perivascular drainage; vascular smooth muscle cells; pericytes;
D O I
10.1016/j.neurobiolaging.2004.02.003
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
For the purposes of this debate here we argue the case that cerebral amyloid angiopathy (CAA) has a direct role in the pathogenesis of Alzheimer's disease (AD). Firstly, there is a very close relationship between CAA and AD and they share genetic risk factors. Secondly, we propose a specific mechanism which puts age-related cerebrovascular degeneration at a crucial point in the pathogenesis of AD as follows. Amyloid beta-protein (Abeta) is normally eliminated from the brain along with extracellular fluid by bulk flow along the perivascular pathway. Age-related fibrosis of cerebral cortical and meningeal arteries leads to impaired drainage of Abeta along the perivascular pathway and, together with the production of Abeta by smooth muscle cells and perivascular cells, is responsible for accumulation of Abeta as CAA. Reduced elimination leads to increased concentration of soluble Abeta in the extracellular fluid of the brain parenchyma. Increased concentration of soluble Abeta leads to the formation of insoluble Abeta plaques, other features of AD pathology, and dementia. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:589 / 597
页数:9
相关论文
共 62 条
[1]   Imaging of amyloid-β deposits in brains of living mice permits direct observation of clearance of plaques with immunotherapy [J].
Backskai, BJ ;
Kajdasz, ST ;
Christie, RH ;
Carter, C ;
Games, D ;
Seubert, P ;
Schenk, D ;
Hyman, BT .
NATURE MEDICINE, 2001, 7 (03) :369-372
[2]   Brain clearance of Alzheimer's amyloid-β40 in the squirrel monkey:: A SPECT study in a primate model of cerebral amyloid angiopathy [J].
Bading, JR ;
Yamada, S ;
Mackic, JB ;
Kirkman, L ;
Miller, C ;
Calero, M ;
Ghiso, J ;
Frangione, B ;
Zlokovic, BV .
JOURNAL OF DRUG TARGETING, 2002, 10 (04) :359-368
[3]   Cholinergic deafferentation of the rabbit cortex:: a new animal model of Aβ deposition [J].
Beach, TG ;
Potter, PE ;
Kuo, YM ;
Emmerling, MR ;
Durham, RA ;
Webster, SD ;
Walker, DG ;
Sue, LI ;
Scott, S ;
Layne, KJ ;
Roher, AE .
NEUROSCIENCE LETTERS, 2000, 283 (01) :9-12
[4]   Neuronal overexpression of mutant amyloid precursor protein results in prominent deposition of cerebrovascular amyloid [J].
Calhoun, ME ;
Burgermeister, P ;
Phinney, AL ;
Stalder, M ;
Tolnay, M ;
Wiederhold, KH ;
Abramowski, D ;
Sturchler-Pierrat, C ;
Sommer, B ;
Staufenbiel, M ;
Jucker, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14088-14093
[5]   DRAINAGE OF BRAIN EXTRACELLULAR FLUID INTO BLOOD AND DEEP CERVICAL LYMPH AND ITS IMMUNOLOGICAL SIGNIFICANCE [J].
CSERR, HF ;
HARLINGBERG, CJ ;
KNOPF, PM .
BRAIN PATHOLOGY, 1992, 2 (04) :269-276
[6]   Evidence that neurones accumulating amyloid can undergo lysis to form amyloid plaques in Alzheimer's disease [J].
D'Andrea, MR ;
Nagele, RG ;
Wang, HY ;
Peterson, PA ;
Lee, DHS .
HISTOPATHOLOGY, 2001, 38 (02) :120-134
[7]   CORTICAL BLOOD-VESSELS OF THE HUMAN-BRAIN [J].
DUVERNOY, HM ;
DELON, S ;
VANNSON, JL .
BRAIN RESEARCH BULLETIN, 1981, 7 (05) :519-579
[8]  
Esiri MM, 2001, LANCET, V357, P169
[9]   SECRETION AND ACCUMULATION OF ALZHEIMERS BETA-PROTEIN BY CULTURED VASCULAR SMOOTH-MUSCLE CELLS FROM OLD AND YOUNG-DOGS [J].
FRACKOWIAK, J ;
MAZURKOLECKA, B ;
WISNIEWSKI, HM ;
POTEMPSKA, A ;
CARROLL, RT ;
EMMERLING, MR ;
KIM, KS .
BRAIN RESEARCH, 1995, 676 (01) :225-230
[10]   Secretion and accumulation of Aβ by brain vascular smooth muscle cells from AβPP-Swedish transgenic mice [J].
Frackowiak, J ;
Miller, DL ;
Potempska, A ;
Sukontasup, T ;
Mazur-Kolecka, B .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2003, 62 (06) :685-696