Zacchetti Daniele, Chieregatti Evelina, Bettegazzi Barbara, Mihailovich Marija, Sousa Vitor Lino, Grohovaz Fabio, Meldolesi Jacopo
Vita-Salute San Raffaele University and San Raffaele Scientific Institute, Milano, Italy.
Neurodegener Dis. 2007;4(2-3):117-26. doi: 10.1159/000101836.
A turning point of research in Alzheimer's disease was undoubtedly the discovery of BACE1, the amyloid-beta precursor protein-cleaving enzyme that initiates the generation of amyloid-beta, the peptide strongly suspected to be responsible for neuronal malfunction and death. Several research groups started a race to identify the best inhibitor of BACE1 activity. On the other hand, basic researchers are evaluating the changes in BACE1 expression and activity with the aim to better understand the pathogenetic process of the disease. Along this second line of research, in the last few years many important results have been reported in various experimental models, as well as in Alzheimer's disease patients. As a consequence, new pathogenetic paradigms have been developed. We have reviewed these reports trying to highlight contrasting viewpoints, data awaiting final confirmation, and promising perspectives.
阿尔茨海默病研究的一个转折点无疑是β-分泌酶1(BACE1)的发现,它是一种切割淀粉样前体蛋白的酶,可启动β淀粉样蛋白的生成,而这种肽被强烈怀疑是导致神经元功能障碍和死亡的原因。几个研究小组展开了竞赛,以确定BACE1活性的最佳抑制剂。另一方面,基础研究人员正在评估BACE1表达和活性的变化,旨在更好地理解该疾病的发病机制。沿着这第二条研究路线,在过去几年中,各种实验模型以及阿尔茨海默病患者都报告了许多重要结果。因此,已经形成了新的发病机制范式。我们回顾了这些报告,试图突出不同的观点、有待最终确认的数据以及有前景的研究方向。