4.7 Article

Altered Balance of Reelin Proteolytic Fragments in the Cerebrospinal Fluid of Alzheimer's Disease Patients

Journal

Publisher

MDPI
DOI: 10.3390/ijms23147522

Keywords

reelin; proteolytic fragment; aggregate; cerebrospinal fluid; biomarker; Alzheimer's disease

Funding

  1. Fondo de Investigaciones Sanitarias [PI15/00665, PI19-01359]
  2. Fondo Europeo de Desarrollo Regional, FEDER Investing in your future
  3. CIBERNED (Instituto de Salud Carlos III, Spain)
  4. Direccio General de Ciencia I Investigacio, Generalitat Valenciana [AICO/2021/308]
  5. Spanish Ministerio de Economia y Competitividad [SEV-2017-0723]
  6. BEFPI fellowship from the Generalitat Valenciana
  7. Swedish Research Council [2018-02532, 2017-00915]
  8. European Research Council [681712]
  9. Swedish State Support for Clinical Research [ALFGBG-720931]
  10. Alzheimer Drug Discovery Foundation (ADDF), USA [201809-2016862, RDAPB-201809-2016615]
  11. AD Strategic Fund
  12. Alzheimer's Association [ADSF-21-831376-C, ADSF-21-831381-C, ADSF-21-831377-C]
  13. Olav Thon Foundation
  14. Erling-Persson Family Foundation
  15. Hjarnfonden, Sweden [FO2019-0228, FO2017-0243]
  16. European Union [860,197]
  17. UK Dementia Research Institute at UCL
  18. Swedish Alzheimer Foundation [AF-742881]
  19. Swedish government [ALFGBG-715986]
  20. European Union Joint Program for Neurodegenerative Disorders [JPND2019-466-236]
  21. National Institute of Health (NIH), USA [1R01AG068398-01]
  22. Alzheimer's Association 2021 Zenith Award [ZEN-21-848495]
  23. Stiftelsen for Gamla Tjanarinnor

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This study examines the differential effects of reelin proteolytic fragments in the cerebrospinal fluid (CSF) of Alzheimer's disease (AD) patients. The study finds that AD patients have decreased levels of full-length reelin and altered expression levels of different reelin fragments. Additionally, the presence of abnormal reelin species with a molecular mass of around 500 kDa is observed in AD samples.
Reelin binds to the apolipoprotein E receptor apoER2 to activate an intracellular signaling cascade. The proteolytic cleavage of reelin follows receptor binding but can also occur independently of its binding to receptors. This study assesses whether reelin proteolytic fragments are differentially affected in the cerebrospinal fluid (CSF) of Alzheimer's disease (AD) subjects. CSF reelin species were analyzed by Western blotting, employing antibodies against the N- and C-terminal domains. In AD patients, we found a decrease in the 420 kDa full-length reelin compared with controls. In these patients, we also found an increase in the N-terminal 310 kDa fragment resulting from the cleavage at the so-called C-t site, whereas the 180 kDa fragment originated from the N-t site remained unchanged. Regarding the C-terminal proteolytic fragments, the 100 kDa fragment resulting from the cleavage at the C-t site also displayed increased levels, whilst the one resulting from the N-t site, the 250 kDa fragment, decreased. We also detected the presence of an aberrant reelin species with a molecular mass of around 500 kDa present in AD samples (34 of 43 cases), while it was absent in the 14 control cases analyzed. These 500 kDa species were only immunoreactive to N-terminal antibodies. We validated the occurrence of these aberrant reelin species in an A beta 42-treated reelin-overexpressing cell model. When we compared the AD samples from APOE genotype subgroups, we only found minor differences in the levels of reelin fragments associated to the APOE genotype, but interestingly, the levels of fragments of apoER2 were lower in APOE epsilon 4 carriers with regards to APOE epsilon 3/epsilon 3. The altered proportion of reelin/apoER2 fragments and the occurrence of reelin aberrant species suggest a complex regulation of the reelin signaling pathway, which results impaired in AD subjects.

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