| Literature DB >> 33566014 |
Ginevra Begani Provinciali1, Nicola Pieroni1, Inna Bukreeva1, Michela Fratini1, Lorenzo Massimi2, Laura Maugeri3, Francesca Palermo1, Fabrizio Bardelli1, Alberto Mittone4, Alberto Bravin4, Giuseppe Gigli5, Francesco Gentile6, Andrea Fossaghi6, Nilo Riva6, Angelo Quattrini6, Alessia Cedola1.
Abstract
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder affecting motor neurons. Pre-clinical studies drive the development of animal models that well mimic ALS disorder and enable both the dissection of disease processes and an early assessment of therapy efficacy. A comprehensive knowledge of neuronal and vascular lesions in the brain and spinal cord is an essential factor to understand the development of the disease. Spatial resolution and bidimensional imaging are important drawbacks limiting current neuroimaging tools, while neuropathology relies on protocols that may alter tissue chemistry and structure. In contrast, recent ex vivo studies in mice demonstrated that X-ray phase-contrast tomography enables study of the 3D distribution of both vasculature and neuronal networks, without sample sectioning or use of staining. Here we present our findings on ex vivo SOD1G93A ALS mice spinal cord at a micrometric scale. An unprecedented direct quantification of neuro-vascular alterations at different stages of the disease is shown. open access.Entities:
Keywords: ALS; X-ray phase contrast tomography; spinal cord
Year: 2020 PMID: 33566014 DOI: 10.1107/S1600577520006785
Source DB: PubMed Journal: J Synchrotron Radiat ISSN: 0909-0495 Impact factor: 2.616