Affiliations: [a]
Douglas Hospital Research Centre, Montréal, QC, Canada
| [b]
Centre for the Studies on the Prevention of Alzheimer’s Disease, Montréal, QC, Canada
| [c]
McGill University, Montréal, QC, Canada
Correspondence:
[*]
Correspondence to: Dr. Judes Poirier, PhD, CQ, Director, Centre for the Studies on the Prevention of Alzheimer’s Disease, Douglas Mental Health University Institute, 6875 Lasalle, Montréal, Québec H4H 1R3, Canada. Tel.: +1 514 761 6131; Ext. 6153; Fax: +1 514 888 4094; E-mail: judes.poirier@mcgill.ca.
Abstract: Background:In mouse models of amyloidosis, macrophage receptor 1 (MSR1) and neprilysin (NEP) have been shown to interact to reduce amyloid burden in the brain. Objective:The purpose of this study is to analyze these two gene products in combination with apolipoproteins and Aβ1-42 in the cerebrospinal fluid (CSF) and plasma of individuals at different stages of Alzheimer’s disease (AD), as well as in autopsied brain samples from ROSMAP (Religious Orders Study and Memory and Aging Project). Methods:CSF/plasma levels of MSR1 and NEP were measured using the sensitive primer extension assay technology. CSF Aβ1-42 was assessed with ELISA, while CSF ApoE and ApoJ were measured with the Luminex’s multiplex technology. Brain MSR1, APOE, and CLU (APOJ) mRNA levels were measured with RNA-Seq and contrasted to amyloid plaques pathology using CERAD staging. Results:While plasma and CSF MSR1 levels are significantly correlated, this correlation was not observed for NEP. In addition to be highly correlated to one another, CSF levels of both MSR1 and NEP are strongly correlated with AD status and CSF Aβ1-42, ApoE, and ApoJ levels. In the cortical tissues of subjects from ROSMAP, MSR1 mRNA levels are correlated with CLU mRNA levels and the CERAD scores but not with APOE mRNA levels. Conclusion:The discrepancies observed between CSF/plasma levels of MSR1 and NEP with CSF Aβ1-42 and ApoE concentrations can be explained by many factors, such as the disease stage or the involvement of the blood-brain barrier breakdown that leads to the infiltration of peripheral monocytes or macrophages.
