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Amyloid-ß Plaques in Clinical Alzheimer's Disease Brain Incorporate Stable Isotope Tracer In Vivo and Exhibit Nanoscale Heterogeneity.
Wildburger, Norelle C; Gyngard, Frank; Guillermier, Christelle; Patterson, Bruce W; Elbert, Donald; Mawuenyega, Kwasi G; Schneider, Theresa; Green, Karen; Roth, Robyn; Schmidt, Robert E; Cairns, Nigel J; Benzinger, Tammie L S; Steinhauser, Matthew L; Bateman, Randall J.
Afiliação
  • Wildburger NC; Department of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
  • Gyngard F; Department of Physics, Washington University in St. Louis, St. Louis, MO, United States.
  • Guillermier C; NanoImaging Center, Division of Genetics, Brigham and Women's Hospital, Cambridge, MA, United States.
  • Patterson BW; Brigham and Women's Hospital, Boston, MA, United States.
  • Elbert D; Harvard Medical School, Boston, MA, United States.
  • Mawuenyega KG; Department of Medicine, Washington University School of Medicine, St. Louis, MO, United States.
  • Schneider T; Department of Neurology, The University of Texas at Austin Dell Medical School, Austin, TX, United States.
  • Green K; Department of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
  • Roth R; Department of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
  • Schmidt RE; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Cairns NJ; Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, United States.
  • Benzinger TLS; Washington University Center for Cellular Imaging, Washington University School of Medicine, St. Louis, MO, United States.
  • Steinhauser ML; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, United States.
  • Bateman RJ; Department of Neurology, Washington University School of Medicine, St. Louis, MO, United States.
Front Neurol ; 9: 169, 2018.
Article em En | MEDLINE | ID: mdl-29623063
ABSTRACT
Alzheimer's disease (AD) is a neurodegenerative disorder with clinical manifestations of progressive memory decline and loss of executive function and language. AD affects an estimated 5.3 million Americans alone and is the most common form of age-related dementia with a rapidly growing prevalence among the aging population-those 65 years of age or older. AD is characterized by accumulation of aggregated amyloid-beta (Aß) in the brain, which leads to one of the pathological hallmarks of AD-Aß plaques. As a result, Aß plaques have been extensively studied after being first described over a century ago. Advances in brain imaging and quantitative measures of Aß in biological fluids have yielded insight into the time course of plaque development decades before and after AD symptom onset. However, despite the fundamental role of Aß plaques in AD, in vivo measures of individual plaque growth, growth distribution, and dynamics are still lacking. To address this question, we combined stable isotope labeling kinetics (SILK) and nanoscale secondary ion mass spectrometry (NanoSIMS) imaging in an approach termed SILK-SIMS to resolve plaque dynamics in three human AD brains. In human AD brain, plaques exhibit incorporation of a stable isotope tracer. Tracer enrichment was highly variable between plaques and the spatial distribution asymmetric with both quiescent and active nanometer sub-regions of tracer incorporation. These data reveal that Aß plaques are dynamic structures with deposition rates over days indicating a highly active process. Here, we report the first, direct quantitative measures of in vivo deposition into plaques in human AD brain. Our SILK-SIMS studies will provide invaluable information on plaque dynamics in the normal and diseased brain and offer many new avenues for investigation into pathological mechanisms of the disease, with implications for therapeutic development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Neurol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Front Neurol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos