4.7 Article

Exploring Alzheimer's disease mouse brain through X-ray phase contrast tomography: From the cell to the organ

期刊

NEUROIMAGE
卷 184, 期 -, 页码 490-495

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2018.09.044

关键词

Alzheimer disease neuropathology; Beta-amyloid plaques; Animal model; X-ray phase contrast tomography; Synchrotron radiation

资金

  1. European project VOXEL Volumetric Medical X-Ray Imaging at extremely low dose (HORIZON 2020-Fet Open) [665207]
  2. Paul Allen Foundation [12069]
  3. Italian Ministry of Health [GR-2013-02358177]

向作者/读者索取更多资源

Alzheimer's disease (AD), the most common form of dementia, is a progressive neurodegenerative disorder associated with aberrant production of beta-amyloid (A beta) peptide depositing in brain as amyloid plaques. While animal models allow investigation of disease progression and therapeutic efficacy, technology to fully dissect the pathological mechanisms of this complex disease at cellular and vascular levels is lacking. X-ray phase contrast tomography (XPCT) is an advanced non-destructive 3D multi-scale direct imaging from the cell through to the whole brain, with exceptional spatial and contrast resolution. We exploit XPCT to simultaneously analyse disease-relevant vascular and neuronal networks in AD mouse brain, without sectioning and staining. The findings clearly show the different typologies and internal structures of A beta plaques, together with their interaction with patho/physiological cellular and neuro-vascular microenvironment. XPCT enables for the first time a detailed visualization of amyloid-angiopathy at capillary level, which is impossible to achieve with other approaches. XPCT emerges as added-value technology to explore AD mouse brain as a whole, preserving tissue chemistry and structure, enabling the comparison of physiological vs. pathological states at the level of crucial disease targets. In-vivo translation will permit to monitor emerging therapeutic approaches and possibly shed new light on pathological mechanisms of neurodegenerative diseases.

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