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β-位点淀粉样前体蛋白裂解酶在阿尔茨海默病中的表达与活性

Expression and activity of beta-site amyloid precursor protein cleaving enzyme in Alzheimer's disease.

作者信息

Johnston J A, Liu W W, Todd S A, Coulson D T R, Murphy S, Irvine G B, Passmore A P

机构信息

School of Biology and Biochemistry, The Queen's University of Belfast, Medical Biology Centre, Belfast BT9 7BL, Northern Ireland.

出版信息

Biochem Soc Trans. 2005 Nov;33(Pt 5):1096-100. doi: 10.1042/BST20051096.

Abstract

Several lines of evidence indicate that the Abeta peptide is involved at some level in the pathological process that results in the clinical symptoms of AD (Alzheimer's disease). The N-terminus of Abeta is generated by cleavage of the Met-Asp bond at position 671-672 of APP (amyloid precursor protein), catalysed by a proteolytic activity called beta-secretase. Two 'beta-secretase' proteases have been identified: BACE (beta-site APP-cleaving enzyme) and BACE2. The cause of sporadic AD is currently unknown, but some studies have reported elevated BACE/beta-secretase activity in brain regions affected by the disease. We have demonstrated that robust beta-secretase activity is also detectable in platelets that contain APP and release Abeta. This review considers the current evidence for alterations in beta-secretase activity, and/or alterations in BACE expression, in post-mortem brain tissue and platelets from individuals with AD.

摘要

多条证据表明,β淀粉样肽在某种程度上参与了导致阿尔茨海默病(AD)临床症状的病理过程。β淀粉样肽的N端是由APP(淀粉样前体蛋白)第671 - 672位的Met - Asp键在一种名为β分泌酶的蛋白水解活性催化下裂解产生的。已鉴定出两种“β分泌酶”蛋白酶:BACE(β位点APP裂解酶)和BACE2。散发性AD的病因目前尚不清楚,但一些研究报告称,在受该疾病影响的脑区中,BACE/β分泌酶活性升高。我们已经证明,在含有APP并释放β淀粉样肽的血小板中也可检测到较强的β分泌酶活性。本综述考虑了目前关于AD患者死后脑组织和血小板中β分泌酶活性改变和/或BACE表达改变的证据。

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