Virtual histology of Alzheimer’s Disease: why are amyloid-β plaques visible with X-ray phase-contrast imaging? - Synchrotron Soleil Accéder directement au contenu
Article Dans Une Revue Acta Biomaterialia Année : 2022

Virtual histology of Alzheimer’s Disease: why are amyloid-β plaques visible with X-ray phase-contrast imaging?

Histologie virtuelle de la maladie d'Alzheimer: pourquoi les plaques β-amyloïdes sont-elles visibles en imagerie X par contraste de phase?

Christophe Sandt
Timm Weitkamp
Tanja Dučić
Thierry Baron

Résumé

Abstract Amyloid-β (Aβ) plaques from Alzheimer’s Disease (AD) can be visualized ex vivo in label-free brain samples using synchrotron X-ray phase-contrast to-mography (XPCT). However, for XPCT to be useful as a screening method for amyloid pathology, it is mandatory to understand which factors drive the detection of Aβ plaques. The current study was designed to test the hypothesis that the Aβ–related contrast in XPCT could be caused by the Aβ fibrils and/or by metal entrapment within the Aβ plaques. This study probed the fibrillar and elemental compositions of Aβ plaques in brain samples from different types of AD patients and different AD animal models to establish a relationship between XPCT contrast and Aβ plaque characteristics. XPCT, micro-Fourier-Transform Infrared (µFTIR) spectroscopy and micro-X-Ray Fluorescence (µXRF) spectroscopy were conducted under synchrotron radiation on human samples (genetic and sporadic cases) and on four transgenic rodent strains (mouse: APPPS1, ArcAβ, J20; rat: TgF344). Aβ plaques from the genetic AD patient were visible using XPCT, and had higher β–sheet content and higher metal levels than those from the sporadic AD patient, which remained undetected by XPCT. Aβ plaques in J20 mice and TgF344 rats appeared hyperintense on XPCT images, while they were hypointense in the case of APPPS1 and ArcAβ mice. In all four transgenic strains, β-sheet content was similar, while metal levels were highly variable: J20 mice (zinc and iron), and TgF344 (copper) showed greater metal accumulation than APPPS1 and ArcAβ mice. In humans, the greater and more diffuse metal accumulation led to a positive contrast in the genetic case of AD. Hence, contrast formation of Aβ plaques in XPCT images depended mostly on biometal entrapment. Graphical Abstract Highlights Amyloid-β plaques in the different forms of Alzheimer’s Disease have various contrasts in X-ray phase-contrast tomography In transgenic rodents, a core-restricted, positive contrast is driven by the level of metal entrapment within plaques In humans, greater and more diffuse metal accumulation lead to a positive contrast in a genetic case of AD
Fichier principal
Vignette du fichier
Chourrout et al. - 2022 - Virtual histology of Alzheimer’s Disease why are .pdf (31.85 Mo) Télécharger le fichier
Origine : Fichiers produits par l'(les) auteur(s)
licence : CC BY NC ND - Paternité - Pas d'utilisation commerciale - Pas de modification

Dates et versions

hal-04046962 , version 1 (27-03-2023)
hal-04046962 , version 2 (19-10-2023)

Licence

Paternité - Pas d'utilisation commerciale - Pas de modification

Identifiants

Citer

Matthieu Chourrout, Christophe Sandt, Timm Weitkamp, Tanja Dučić, David Meyronet, et al.. Virtual histology of Alzheimer’s Disease: why are amyloid-β plaques visible with X-ray phase-contrast imaging?. Acta Biomaterialia, 2022, 170, pp.260-272. ⟨10.1016/j.actbio.2023.07.046⟩. ⟨hal-04046962v1⟩
121 Consultations
6 Téléchargements

Altmetric

Partager

Gmail Facebook X LinkedIn More