Secretases as therapeutic targets for the treatment of Alzheimer's disease

被引:30
作者
Dominguez, DI
De Strooper, B
Annaert, W
机构
[1] Katholieke Univ Leuven, Neuronal Cell Biol & Gene Transfer Lab, Ctr Human Genet, B-3000 Louvain, Belgium
[2] Flanders Interuniv Inst Biotechnol, B-3000 Louvain, Belgium
来源
AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS | 2001年 / 8卷 / 02期
关键词
secretase; ADAM-10; BACE; presenilin; A beta PP; Alzheimer's disease;
D O I
10.3109/13506120109007356
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
The extracellular deposition of short amyloid peptides in the brain of patients is thought to be a central event in the pathogenesis of Alzheimer's Disease. The generation of the amyloid peptide occurs via a regulated cascade of cleavage events in its precursor protein, A beta PP. Ar least three enzymes are responsible for A beta PP proteolysis and have been tentatively named alpha-, beta and gamma -secretases. The recent identification of several of these secretases is a major leap in the understanding how these secretases regulate amyloid peptide formation. Members of the ADAM family of metalloproteases are involved in the non-amyloidogenic secretase pathway. The amyloidogenic counterpart pathway is initiated by the recently cloned novel aspartate protease named BACE. The available data are conclusive and crown BACE as the long-sought beta -secretase. This enzyme is a prime candidate drug target for the development of therapy aiming to lower the amyloid bla den in the disease. Finally, the gamma -secretases are intimately linked to the function of the presenilins. These multi-transmembrane domain proteins remain intriguing study objects. The hypothesis that the presenilins constitute a complete novel type of protease family, and are cleaving A beta PP within the transmembrane region, remains an issue of debate. Several questions remain unanswered and direct proof that they exert catalytic activity is still lacking. The subcellular localization of presenilins in neurons, their integration in functional multiprotein complexes and the recent identification of additional modulators of gamma -secretase, like nicastrin, indicate already that several players are involved. Nevertheless, the rapidly increasing knowledge in this area is already paving the road towards selective inhibitors of this secretase as well. It is hoped that such drugs, possibly in concert with the experimental vaccination therapies that are currently tested, will lead to a cure of this inexorable disease.
引用
收藏
页码:124 / 142
页数:19
相关论文
共 260 条
[51]   PROCESSING OF THE PRE-BETA-AMYLOID PROTEIN BY CATHEPSIN-D IS ENHANCED BY A FAMILIAL ALZHEIMERS-DISEASE MUTATION [J].
DREYER, RN ;
BAUSCH, KM ;
FRACASSO, P ;
HAMMOND, LJ ;
WUNDERLICH, D ;
WIRAK, DO ;
DAVIS, G ;
BRINI, CM ;
BUCKHOLZ, TM ;
KONIG, G ;
KAMARCK, ME ;
TAMBURINI, PP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 224 (02) :265-271
[52]   Increased amyloid-beta 42(43) in brains of mice expressing mutant presenilin 1 [J].
Duff, K ;
Eckman, C ;
Zehr, C ;
Yu, X ;
Prada, CM ;
Pereztur, J ;
Hutton, M ;
Buee, L ;
Harigaya, Y ;
Yager, D ;
Morgan, D ;
Gordon, MN ;
Holcomb, L ;
Refolo, L ;
Zenk, B ;
Hardy, J ;
Younkin, S .
NATURE, 1996, 383 (6602) :710-713
[53]   Rank-order of potencies for inhibition of the secretion of Aβ40 and Aβ42 suggests that both are generated by a single γ-secretase [J].
Durkin, JT ;
Murthy, S ;
Husten, EJ ;
Trusko, SP ;
Savage, MJ ;
Rotella, DP ;
Greenberg, BD ;
Siman, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (29) :20499-20504
[54]   A new pathogenic mutation in the APP gene (1716V) increases the relative proportion of A beta 42(43) [J].
Eckman, CB ;
Mehta, ND ;
Crook, R ;
Pereztur, J ;
Prihar, G ;
Pfeiffer, E ;
GraffRadford, N ;
Hinder, P ;
Yager, D ;
Zenk, B ;
Refolo, LM ;
Prada, CM ;
Younkin, SG ;
Hutton, M ;
Hardy, J .
HUMAN MOLECULAR GENETICS, 1997, 6 (12) :2087-2089
[55]  
Eisenhauer PB, 2000, J NEUROSCI RES, V60, P804, DOI 10.1002/1097-4547(20000615)60:6<804::AID-JNR13>3.3.CO
[56]  
2-T
[57]   CLEAVAGE OF AMYLOID-BETA PEPTIDE DURING CONSTITUTIVE PROCESSING OF ITS PRECURSOR [J].
ESCH, FS ;
KEIM, PS ;
BEATTIE, EC ;
BLACHER, RW ;
CULWELL, AR ;
OLTERSDORF, T ;
MCCLURE, D ;
WARD, PJ .
SCIENCE, 1990, 248 (4959) :1122-1124
[58]   Transition-state analogue inhibitors of γ-secretase bind directly to presenilin-1 [J].
Esler, WP ;
Kimberly, WT ;
Ostaszewski, BL ;
Diehl, TS ;
Moore, CL ;
Tsai, JY ;
Rahmati, T ;
Xia, WM ;
Selkoe, DJ ;
Wolfe, MS .
NATURE CELL BIOLOGY, 2000, 2 (07) :428-434
[59]   PREVALENCE OF ALZHEIMERS-DISEASE IN A COMMUNITY POPULATION OF OLDER PERSONS - HIGHER THAN PREVIOUSLY REPORTED [J].
EVANS, DA ;
FUNKENSTEIN, H ;
ALBERT, MS ;
SCHERR, PA ;
COOK, NR ;
CHOWN, MJ ;
HEBERT, LE ;
HENNEKENS, CH ;
TAYLOR, JO .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 262 (18) :2551-2556
[60]   BACE2, a β-secretase homolog, cleaves at the β site and within the amyloid-β region of the amyloid-β precursor protein [J].
Farzan, M ;
Schnitzler, CE ;
Vasilieva, N ;
Leung, D ;
Choe, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (17) :9712-9717