Amyloid fibril polymorphism: a challenge for molecular imaging and therapy

M. Fändrich, S. Nyström, K. P.R. Nilsson, A. Böckmann, H. LeVine, P. Hammarström

Research output: Contribution to journalArticlepeer-review

101 Scopus citations

Abstract

The accumulation of misfolded proteins (MPs), both unique and common, for different diseases is central for many chronic degenerative diseases. In certain patients, MP accumulation is systemic (e.g. TTR amyloid), and in others, this is localized to a specific cell type (e.g. Alzheimer's disease). In neurodegenerative diseases, NDs, it is noticeable that the accumulation of MP progressively spreads throughout the nervous system. Our main hypothesis of this article is that MPs are not only markers but also active carriers of pathogenicity. Here, we discuss studies from comprehensive molecular approaches aimed at understanding MP conformational variations (polymorphism) and their bearing on spreading of MPs, MP toxicity, as well as MP targeting in imaging and therapy. Neurodegenerative disease (ND) represents a major and growing societal challenge, with millions of people worldwide suffering from Alzheimer's or Parkinson's diseases alone. For all NDs, current treatment is palliative without addressing the primary cause and is not curative. Over recent years, particularly the shape-shifting properties of misfolded proteins and their spreading pathways have been intensively researched. The difficulty in addressing ND has prompted most major pharma companies to severely downsize their nervous system disorder research. Increased academic research is pivotal for filling this void and to translate basic research into tools for medical professionals. Recent discoveries of targeting drug design against MPs and improved model systems to study structure, pathology spreading and toxicity strongly encourage future studies along these lines to provide an opportunity for selective imaging, prognostic diagnosis and therapy.

Original languageEnglish
Pages (from-to)218-237
Number of pages20
JournalJournal of Internal Medicine
Volume283
Issue number3
DOIs
StatePublished - Mar 2018

Bibliographical note

Publisher Copyright:
© 2018 The Association for the Publication of the Journal of Internal Medicine

Funding

Dr. Hammarstro€m reports grants from The Swedish Research Council, grants from The Go€ran Gustafsson Foundation, grants from The Swedish Alzheimer Foundation. Dr. Nystro€m reports a grant from the Swedish Alzheimer Foundation, Dr. Nilsson reports a grant from the Swedish Research Council, Dr. LeVine reports grants from NIH/NINDS, grants from BrightFocus Foundation, Dr. Bo€ckmann reports a grant from the French ANR, Dr. Fa€ndrich reports a grant from the Deutsche Forschungsgemeinschaft, during the conduct of the study; Dr. Hammarstro€m, Dr. Nystro€m and Dr. Nilsson are shareholders of Furcifer AB, a company that founded Ebba Biotech AB, who makes some of the amyloid ligands described in the paper available to researchers globally. In addition, Dr. Nilsson has a patent issued. Our work was funded by the Swedish Research Council (2015-04521, 2015-05868), the Göran Gustafsson Foundation, the Swedish Alzheimer Foundation, Linköping University, NIH/NINDS (R21 NS080576), BrightFocus Foundation (A2014044S), the French ANR (ANR-14-CE09-0024B) and the Deutsche Forschungsgemeinschaft (FA 456/15-1). Our work was funded by the Swedish Research Council (2015-04521, 2015-05868), the Go€ran Gustafsson Foundation, the Swedish Alzheimer Foundation, Linko€ping University, NIH/NINDS (R21 NS080576), BrightFocus Foundation (A2014044S), the French ANR (ANR-14-CE09-0024B) and the Deutsche Forschungsgemein-schaft (FA 456/15-1).

FundersFunder number
Ebba Biotech AB
Furcifer AB
National Institutes of Health (NIH)
National Institute of Neurological Disorders and StrokeR21NS080576
BrightFocus FoundationA2014044S, ANR-14-CE09-0024B
Göran Gustafssons Stiftelser
Deutsche ForschungsgemeinschaftFA 456/15-1
Agence Nationale de la Recherche
Göran Gustafssons Stiftelse för Naturvetenskaplig och Medicinsk Forskning
Linköpings Universitet
Vetenskapsrådet2015-04521, 2015-05868
Alzheimerfonden

    Keywords

    • Alzheimer's disease
    • amyloidosis
    • biochemistry
    • chronic diseases
    • pathology

    ASJC Scopus subject areas

    • Internal Medicine

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