Institute of Biosciences and BioResources, National Research Council (CNR-IBBR), Napoli, Italy.
Institute of Biostructure and Bioimaging, National Research Council (CNR-IBB), Napoli, Italy.
J Alzheimers Dis. 2017;60(3):1097-1106. doi: 10.3233/JAD-170389.
Alzheimer's disease (AD) is a progressive, multifactorial neurodegenerative disorder that is the main cause of dementia. To date, there are no definitive diagnostic tests that can predict or assess onset and progression of the disease. Blood biomarkers for AD are being sought for many years but their identification remains a challenging task. In this study, we investigated the potential relationship between AD and levels of acyl-peptide hydrolase (APEH) and proteasome in erythrocyte samples of 52 participants (26 AD and 26 cognitively healthy controls). A statistically significant decrease in proteasome and exopeptidase/endopeptidase APEH activities was found in AD samples compared to those of healthy controls. Moreover, in contrast to what was observed for proteasome transcripts, APEH activities reduction in AD patients was unrelated to its gene expression levels, suggesting the occurrence of posttranslational modifications or the expression of endogenous inhibitors that might impair enzyme activity. These preliminary data further support a relationship between the APEH-proteasome system and AD molecular players, providing the first evidence of its potential use as a novel blood-based indicator for the routine detection of AD.
阿尔茨海默病(AD)是一种进行性、多因素的神经退行性疾病,是痴呆的主要病因。迄今为止,尚无明确的诊断测试可以预测或评估疾病的发病和进展。多年来一直在寻找用于 AD 的血液生物标志物,但它们的鉴定仍然是一项具有挑战性的任务。在这项研究中,我们研究了 AD 与红细胞样本中酰肽水解酶(APEH)和蛋白酶体水平之间的潜在关系,参与者共有 52 人(26 名 AD 患者和 26 名认知健康对照者)。与健康对照组相比,AD 样本中的蛋白酶体和外肽酶/内肽酶 APEH 活性明显降低。此外,与蛋白酶体转录本观察到的情况相反,AD 患者 APEH 活性的降低与其基因表达水平无关,这表明发生了翻译后修饰或表达内源性抑制剂,可能会损害酶活性。这些初步数据进一步支持 APEH-蛋白酶体系统与 AD 分子标志物之间的关系,为其作为一种新型基于血液的 AD 常规检测指标的潜在用途提供了首个证据。