Upregulated Expression of Heparanase and Heparanase 2 in the Brains of Alzheimer’s Disease

• Published in: Journal of Alzheimer's disease 2017-01, Vol.58 (1), p.185-192
• Main Authors: 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
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - pathology; Alzheimer Disease - physiopathology; Alzheimer's disease; Brain; Brain - enzymology; Cores; Disease resistance; Female; Fibrillogenesis; Glucuronidase - genetics; Glucuronidase - metabolism; Heparan sulfate; Heparan sulfate proteoglycans; Humans; Immunohistochemistry; Male; Middle Aged; Neurodegenerative diseases; Pathology; Polymerase chain reaction; Proteins; Proteoglycans; Proteolysis; RNA, Messenger - metabolism; Senile plaques; Sulfates; Tau protein; Transcription; Up-Regulation - physiology; β-Amyloid
• ISSN: 1387-2877; 1875-8908
• DOI: 10.3233/JAD-161298

Background: 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. Objective: To analyze HPSE and HPSE2 expressions at different stages of AD. Methods: 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. Results: 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. Conclusion: 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.