García Beatriz, Martín Carla, García-Suárez Olivia, Muñiz-Alonso Bárbara, Ordiales Helena, Fernández-Menéndez Santiago, Santos-Juanes Jorge, Lorente-Gea Laura, Castañón Sonia, Vicente-Etxenausia Ikerne, Piña Batista Kelvin Manuel, Ruiz-Díaz Irune, Caballero-Martínez María Cristina, Merayo-Lloves Jesús, Guerra-Merino Isabel, Quirós Luis M, Fernández-Vega Iván
Department of Functional Biology, University of Oviedo, Spain.
Instituto Universitario Fernández-Vega, Oviedo, Spain.
J Alzheimers Dis. 2017;58(1):185-192. doi: 10.3233/JAD-161298.
Heparan sulfate proteoglycans (HSPGs) promote amyloid-β peptide and tau fibrillization in Alzheimer's disease (AD) and provide resistance against proteolytic breakdown. Heparanase (HPSE) is the only enzyme that cleaves heparan sulfate (HS). Heparanase 2 (HPSE2) lacks HS-degrading activity, although it is able to interact with HS with high affinity.
To analyze HPSE and HPSE2 expressions at different stages of AD.
RT-PCR was used to analyze transcription levels of both heparanases at different stages of AD, and immunohistochemistry was performed to localize each one in different parts of the brain.
Both proteins appeared overexpressed at different stages of AD. Immunohistochemistry indicated that the presence of the heparanases was related to AD pathology, with intracellular deposits found in degenerated neurons. At the extracellular level, HPSE was observed only in neuritic plaques with a fragmented core, while HPSE2 appeared in those with compact cores as well.
Given the involvement of HSPGs in AD pathology, there would seem to be a relationship between the regulation of heparanase expression, the features of the disease, and a possible therapeutic alternative.
硫酸乙酰肝素蛋白聚糖(HSPGs)在阿尔茨海默病(AD)中促进淀粉样β肽和tau蛋白纤维化,并提供抗蛋白水解降解的能力。乙酰肝素酶(HPSE)是唯一能切割硫酸乙酰肝素(HS)的酶。乙酰肝素酶2(HPSE2)虽然能够与HS高亲和力相互作用,但缺乏HS降解活性。
分析AD不同阶段HPSE和HPSE2的表达情况。
采用逆转录聚合酶链反应(RT-PCR)分析AD不同阶段两种乙酰肝素酶的转录水平,并进行免疫组织化学以在脑的不同部位定位每种酶。
两种蛋白在AD的不同阶段均出现过表达。免疫组织化学表明,乙酰肝素酶的存在与AD病理学相关,在退化的神经元中发现细胞内沉积物。在细胞外水平,仅在核心破碎的神经炎性斑块中观察到HPSE,而HPSE2也出现在核心致密的斑块中。
鉴于HSPGs参与AD病理学,乙酰肝素酶表达的调节、疾病特征和可能的治疗选择之间似乎存在关联。