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MFG-E8 (LACTADHERIN): a novel marker associated with cerebral amyloid angiopathy.

Authors :
Marazuela, Paula
Solé, Montse
Bonaterra-Pastra, Anna
Pizarro, Jesús
Camacho, Jessica
Martínez-Sáez, Elena
Kuiperij, H. Bea
Verbeek, Marcel M.
de Kort, Anna M.
Schreuder, Floris H. B. M.
Klijn, Catharina J. M.
Castillo-Ribelles, Laura
Pancorbo, Olalla
Rodríguez-Luna, David
Pujadas, Francesc
Delgado, Pilar
Hernández-Guillamon, Mar
Source :
Acta Neuropathologica Communications; 9/16/2021, Vol. 9 Issue 1, p1-17, 17p
Publication Year :
2021

Abstract

Brain accumulation of amyloid-beta (Aβ) is a crucial feature in Alzheimer´s disease (AD) and cerebral amyloid angiopathy (CAA), although the pathophysiological relationship between these diseases remains unclear. Numerous proteins are associated with Aβ deposited in parenchymal plaques and/or cerebral vessels. We hypothesized that the study of these proteins would increase our understanding of the overlap and biological differences between these two pathologies and may yield new diagnostic tools and specific therapeutic targets. We used a laser capture microdissection approach combined with mass spectrometry in the APP23 transgenic mouse model of cerebral-β-amyloidosis to specifically identify vascular Aβ-associated proteins. We focused on one of the main proteins detected in the Aβ-affected cerebrovasculature: MFG-E8 (milk fat globule-EGF factor 8), also known as lactadherin. We first validated the presence of MFG-E8 in mouse and human brains. Immunofluorescence and immunoblotting studies revealed that MFG-E8 brain levels were higher in APP23 mice than in WT mice. Furthermore, MFG-E8 was strongly detected in Aβ-positive vessels in human postmortem CAA brains, whereas MFG-E8 was not present in parenchymal Aβ deposits. Levels of MFG-E8 were additionally analysed in serum and cerebrospinal fluid (CSF) from patients diagnosed with CAA, patients with AD and control subjects. Whereas no differences were found in MFG-E8 serum levels between groups, MFG-E8 concentration was significantly lower in the CSF of CAA patients compared to controls and AD patients. Finally, in human vascular smooth muscle cells MFG-E8 was protective against the toxic effects of the treatment with the Aβ40 peptide containing the Dutch mutation. In summary, our study shows that MFG-E8 is highly associated with CAA pathology and highlights MFG-E8 as a new CSF biomarker that could potentially be used to differentiate cerebrovascular Aβ pathology from parenchymal Aβ deposition. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20515960
Volume :
9
Issue :
1
Database :
Complementary Index
Journal :
Acta Neuropathologica Communications
Publication Type :
Academic Journal
Accession number :
152503481
Full Text :
https://doi.org/10.1186/s40478-021-01257-9