Apolipoprotein Aβ:: Black sheep in a good family

被引:2
作者
Kontush, A [1 ]
机构
[1] Hop La Pitie Salpetriere, INSERM, Unite 551, F-75651 Paris 13, France
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Amyloid-beta (Abeta) has for a long time been thought to play a central role in the pathogenesis of Alzheimer disease (AD). Analysis of available data indicates that Abeta possesses properties of a metal-binding apolipoprotein influencing lipid transport and metabolism. Protection of lipoproteins from oxidation by transition metals, synaptic activity and role in the acute phase response represent plausible physiological functions of Abeta. However, these important biochemical qualities which may critically influence the development of AD, have been largely ignored by mainstream AD researchers, making Abeta appear to be a "black sheep" in a "good apolipoprotein" family. New studies are needed to shed further light on the physiological role of Abeta in lipid metabolism in the brain.
引用
收藏
页码:433 / 447
页数:15
相关论文
共 214 条
[1]
Andorn Anne C., 2000, Journal of Alzheimer's Disease, V2, P69
[2]
Time-course of oxidation of lipids in human cerebrospinal fluid in vitro [J].
Arlt, S ;
Finckh, B ;
Beisiegel, U ;
Kontush, A .
FREE RADICAL RESEARCH, 2000, 32 (02) :103-114
[3]
Amyloid-β: redox-metal chelator and antioxidant [J].
Atwood, C. S. ;
Robinson, S. R. ;
Smith, M. A. .
JOURNAL OF ALZHEIMERS DISEASE, 2002, 4 (03) :203-214
[4]
Amyloid-β:: a chameleon walking in two worlds:: a review of the trophic and toxic properties of amyloid-β [J].
Atwood, CS ;
Obrenovich, ME ;
Liu, TB ;
Chan, H ;
Perry, G ;
Smith, MA ;
Martins, RN .
BRAIN RESEARCH REVIEWS, 2003, 43 (01) :1-16
[5]
Atwood CS, 2000, CELL MOL BIOL, V46, P777
[6]
Dramatic aggregation of Alzheimer Aβ by Cu(II) is induced by conditions representing physiological acidosis [J].
Atwood, CS ;
Moir, RD ;
Huang, XD ;
Scarpa, RC ;
Bacarra, NME ;
Romano, DM ;
Hartshorn, MK ;
Tanzi, RE ;
Bush, AI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :12817-12826
[7]
Characterization of copper interactions with Alzheimer amyloid β peptides:: Identification of an attomolar-affinity copper binding site on amyloid β1-42 [J].
Atwood, CS ;
Scarpa, RC ;
Huang, XD ;
Moir, RD ;
Jones, WD ;
Fairlie, DP ;
Tanzi, RE ;
Bush, AI .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (03) :1219-1233
[8]
Copper mediates dityrosine cross-linking of Alzheimer's amyloid-β [J].
Atwood, CS ;
Perry, G ;
Zeng, H ;
Kato, Y ;
Jones, WD ;
Ling, KQ ;
Huang, XD ;
Moir, RD ;
Wang, DD ;
Sayre, LM ;
Smith, MA ;
Chen, SG ;
Bush, AI .
BIOCHEMISTRY, 2004, 43 (02) :560-568
[9]
High density lipoproteins (HDLs) and atherosclerosis; the unanswered questions [J].
Barter, P ;
Kastelein, J ;
Nunn, A ;
Hobbs, R .
ATHEROSCLEROSIS, 2003, 168 (02) :195-211
[10]
Cerebrospinal fluid lipoproteins are more vulnerable to oxidation in Alzheimer's disease and are neurotoxic when oxidized ex vivo [J].
Bassett, CN ;
Neely, MD ;
Sidell, KR ;
Markesbery, WR ;
Swift, LL ;
Montine, TJ .
LIPIDS, 1999, 34 (12) :1273-1280