Brain virtual histology with X-ray phase-contrast tomography Part II: 3D morphologies of amyloid-β plaques in Alzheimer’s disease models

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Chourrout, Matthieu | Roux, Margaux | Boisvert, Carlie | Gislard, Coralie | Legland, David | Arganda-Carreras, Ignacio | Olivier, Cécile | Peyrin, Françoise | Boutin, Hervé | Rama, Nicolas | Baron, Thierry | Meyronet, David | Brun, Emmanuel | Rositi, Hugo | Wiart, Marlène | Chauveau, Fabien

Edité par CCSD ; Optical Society of America - OSA Publishing -

International audience. While numerous transgenic mouse strains have been produced to model the formation of amyloid-β (Aβ) plaques in the brain, effi cient methods for whole-brain 3D analysis of Aβ deposits have to be validated and standardized. Moreover, routine immunohistochemistry performed on brain slices precludes any shape analysis of A β plaques, or require complex procedures for serial acquisition and reconstruction. The present study shows how in-line (propagation-based) X-ray phase-contrast tomography (XPCT) combined with ethanol-induced brain sample dehydration enables hippocampus-wide detection and morphometric analysis of Aβ plaques. Performed in three distinct Alzheimer mouse strains, the proposed workflow identified differences in signal intensity and 3D shape parameters: 3xTg displayed a different type of Aβ plaques, with a larger volume and area, greater elongation, flatness and mean breadth, and more intense average signal than J20 and APP/PS1. As a label-free non-destructive technique, XPCT can be combined with standard immunohistochemistry. XPCT virtual histology could thus become instrumental in quantifying the 3D spreading and the morphological impact of seeding when studying prion-like properties of A β aggregates in animal models of Alzheimer’s disease. This is Part II of a series of two articles reporting the value of in-line XPCT for virtual histology of the brain; Part I shows how in-line XPCT enables 3D myelin mapping in the whole rodent brain and in human autopsy brain tissue.

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