LRP1 expression in cerebral cortex, choroid plexus and meningeal blood vessels: Relationship to cerebral amyloid angiopathy and APOE status

• Published in: Neuroscience letters 2012-09, Vol.525 (2), p.123-128
• Main Authors: Ruzali, Wan Adriyani W., Kehoe, Patrick G., Love, Seth
• Format: Article
• Language: English
• Subjects: Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Alzheimer's disease; Apolipoprotein E; Apolipoproteins E - metabolism; Case-Control Studies; Cerebral amyloid angiopathy; Cerebral Amyloid Angiopathy - metabolism; Cerebral Amyloid Angiopathy - pathology; Cerebral Cortex - metabolism; Choroid Plexus - metabolism; Humans; Low Density Lipoprotein Receptor-Related Protein-1 - genetics; Low Density Lipoprotein Receptor-Related Protein-1 - metabolism; Low-density lipoprotein receptor-related protein-1; Meninges - blood supply; RNA, Messenger - metabolism
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2012.07.065

► LRP1 mRNA is elevated in meningeal vessels in association with APOE ɛ4. ► LRP1 mRNA is elevated in choroid plexus and meningeal vessels with AD. ► APOE ɛ2 is associated with decreased LRP1 protein in meningeal vessels with CAA. ► APOE ɛ3 is associated with increased LRP1 protein in choroid plexus with CAA. ► Association of APOE and CAA may be partly mediated through LRP1 in the vasculature and choroid plexus. APOE genotype is a risk factor for Alzheimer's disease (AD) and cerebral amyloid angiopathy (CAA). The risk and severity of CAA increase with possession of APOE ɛ4, whereas APOE ɛ2 increases the risk of vessel rupture. Uptake of Aβ by cerebrovascular smooth muscle cells (CVSMCs) is mediated by low-density lipoprotein receptor-related protein-1 (LRP1). To determine whether APOE influences CAA by altering LRP1 expression, particularly by CVSMCs, we analysed APOE genotype, CAA severity, and LRP1 levels in post-mortem cerebral cortex, choroid plexus and meningeal vessels. LRP1 mRNA and protein were not related to CAA severity and presence. LRP1 mRNA was increased in meningeal vessels, but not cortex or choroid plexus, in AD and in association with APOE ɛ4, and was decreased in association with APOE ɛ3. In brains with CAA, APOE ɛ2 was associated with decreased LRP1 protein in meningeal vessels, and ɛ3 with increased LRP1 in choroid plexus. These findings suggest that APOE may influence the severity of CAA through altered expression of LRP1.