Yan Riqiang
Department of Neurosciences, Lerner Research Institute, Cleveland Clinic Foundation, ClevelandOH, USA.
Front Mol Neurosci. 2017 Apr 19;10:97. doi: 10.3389/fnmol.2017.00097. eCollection 2017.
BACE1 was discovered as the β-secretase for initiating the cleavage of amyloid precursor protein (APP) at the β-secretase site, while its close homology BACE2 cleaves APP within the β-amyloid (Aβ) domain region and shows distinct cleavage preferences . Inhibition of BACE1 proteolytic activity has been confirmed to decrease Aβ generation and amyloid deposition, and thus specific inhibition of BACE1 by small molecules is a current focus for Alzheimer's disease therapy. While BACE1 inhibitors are being tested in advanced clinical trials, knowledge regarding the properties and physiological functions of BACE is highly important and this review summarizes advancements in BACE1 research over the past several years. We and others have shown that BACE1 is not only a critical enzyme for testing the "Amyloid Hypothesis" associated with Alzheimer's pathogenesis, but also important for various functions such as axon growth and pathfinding, astrogenesis, neurogenesis, hyperexcitation, and synaptic plasticity. BACE2 appears to play different roles such as glucose homeostasis and pigmentation. This knowledge regarding BACE1 functions is critical for monitoring the safe use of BACE1 inhibitors in humans.
β-分泌酶1(BACE1)被发现是在β-分泌酶位点启动淀粉样前体蛋白(APP)切割的β-分泌酶,而其同源性相近的BACE2在β-淀粉样蛋白(Aβ)结构域区域内切割APP,并表现出不同的切割偏好。已证实抑制BACE1的蛋白水解活性可减少Aβ生成和淀粉样蛋白沉积,因此小分子对BACE1的特异性抑制是目前阿尔茨海默病治疗的重点。虽然BACE1抑制剂正在进行晚期临床试验,但了解BACE的特性和生理功能非常重要,本综述总结了过去几年BACE1研究的进展。我们和其他人已经表明,BACE1不仅是检验与阿尔茨海默病发病机制相关的“淀粉样蛋白假说”的关键酶,而且对轴突生长和路径寻找、星形胶质细胞生成、神经发生、过度兴奋和突触可塑性等各种功能也很重要。BACE2似乎发挥着不同的作用,如葡萄糖稳态和色素沉着。关于BACE1功能的这些知识对于监测BACE1抑制剂在人体中的安全使用至关重要。