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BACE2 除了 APP 的 β 加工之外,还在脑血管内皮中发挥神经保护作用。

BACE2 beyond β-processing of APP, its neuroprotective role in cerebrovascular endothelium.

机构信息

Instituto de Neurociencias de Alicante, Universidad Miguel Hernández-CSIC, San Juan de Alicante, Alicante, Spain.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

出版信息

J Neurochem. 2023 Sep;166(6):887-890. doi: 10.1111/jnc.15940. Epub 2023 Aug 16.

Abstract

Several proteases are involved in the proteolytic processing of the amyloid precursor protein (APP) generating the amyloidogenic Aβ peptide, which can act as the triggering pathological effector of Alzheimer's disease (AD). Among these proteases, the β-site amyloid precursor protein cleaving enzyme 2 (BACE2) is of particular interest because it was first proposed as an alternative β-secretase to its homolog BACE1; however, accumulating evidence suggests that BACE2 acts as a non-amyloidogenic α-secretase and exerts neuroprotective effects. In this issue of J Neurochem, Katusic et al. present an interesting article reporting that BACE2 plays a role in preservation of cerebral vascular endothelial nitric oxide synthase (eNOS) function, thus exerting protective functions. Their data support that the process is mediated by the large soluble non-amyloidogenic APP fragment sAPPα through the γ-aminobutyric acid type B receptor 1, which enhances the expression of a major transcription factor for eNOS gene expression in endothelial cells, the Krüppel-like factor 2. These protective functions of BACE2 contrast with the pathogenic role of BACE1 as a key player in the AD amyloidogenic pathway. Indeed, many efforts have been invested in BACE1 inhibitors as potential disease modifiers for AD. Unfortunately, the results in clinical trials have been disappointing. In this scenario, a better understanding of the functions of BACE2, as well as the selectivity of BACE1 inhibitors with respect to other β-secretases (mainly BACE2), is crucial for the development of new therapeutic agents. Furthermore, specific cellular targeting should also be considered to improve such therapies due to the diverse balance of secretases targeting APP and the complex cross-talk between them and the generated APP fragments.

摘要

几种蛋白酶参与淀粉样前体蛋白(APP)的蛋白水解加工,生成淀粉样β肽(Aβ肽),后者可作为阿尔茨海默病(AD)的触发病理效应物。在这些蛋白酶中,β-位点 APP 裂解酶 2(BACE2)特别引人注目,因为它最初被提议作为其同源物 BACE1 的替代β-分泌酶;然而,越来越多的证据表明,BACE2 作为一种非淀粉样β-分泌酶发挥作用,并具有神经保护作用。在本期《神经化学杂志》中,Katusic 等人发表了一篇有趣的文章,报道 BACE2 在外周血内皮型一氧化氮合酶(eNOS)功能的保护中发挥作用,从而发挥保护作用。他们的数据支持该过程是通过大的可溶性非淀粉样β-分泌酶 APP 片段 sAPPα 介导的,通过γ-氨基丁酸 B 型受体 1,增强内皮细胞中 eNOS 基因表达的主要转录因子 Krüppel 样因子 2 的表达。BACE2 的这些保护作用与 BACE1 在 AD 淀粉样形成途径中的致病作用形成对比。事实上,人们投入了大量精力研究 BACE1 抑制剂作为 AD 的潜在疾病修饰剂。不幸的是,临床试验的结果令人失望。在这种情况下,更好地了解 BACE2 的功能,以及 BACE1 抑制剂相对于其他β-分泌酶(主要是 BACE2)的选择性,对于开发新的治疗剂至关重要。此外,还应考虑特定的细胞靶向,以改善这些疗法,因为靶向 APP 的分泌酶的多样性平衡以及它们之间的复杂相互作用以及生成的 APP 片段。

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