The functional γ-secretase inhibitor prevents production of amyloid β 1-34 in human and murine cell lines

被引:39
作者
Vandermeeren, M
Geraerts, M
Pype, S
Dillen, L
Van Hove, C
Mercken, M
机构
[1] Janssen Res Fdn, CNS Discovery Res, B-2340 Beerse, Belgium
[2] Janssen Res Fdn, Genom Technol, B-2340 Beerse, Belgium
关键词
gamma-secretase; Alzheimer's disease; amyloid beta peptides; BACE-1; amyloid; mass spectrometry;
D O I
10.1016/S0304-3940(01)02369-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The amyloid precursor protein (APP) undergoes two consecutive cleavages by different proteases, beta -secretase and gamma -secretase, leading to the release of an amyloidogenic 4 kDa fragment called amyloid beta (A beta). Combining immunoprecipitation and mass spectrometry, we characterized soluble A beta in cultured cell media of mouse neuroblastoma N2a cells and double hAPP/hBACE-1 transfected HEK293. The major A beta isoforms detected were A beta 11-34, A beta1-34, A beta 11-40 and A beta1-40. In this study, we demonstrate that overexpression of human beta -secretase (BACE-1) in HEK293 cells resulted in predominant A beta cleavage at position Glu(11) rather than Asp(1), as well as increased production of A betax-34, but not A betax-40. Incubation of cells with a specific gamma -secretase inhibitor suggests that cleavage of APP at Leu(34) could be mediated by gamma -secretase itself or by a gamma -secretase dependent process. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:145 / 148
页数:4
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