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mHTT seeding activity: a marker of disease progression and neurotoxicity in models of Huntington's disease

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Item Type:Article
Title:mHTT seeding activity: a marker of disease progression and neurotoxicity in models of Huntington's disease
Creators Name:Ast, A., Buntru, A., Schindler, F., Hasenkopf, R., Schulz, A., Brusendorf, L., Klockmeier, K., Grelle, G., McMahon, B., Niederlechner, H., Jansen, I., Diez, L., Edel, J., Boeddrich, A., Franklin, S.A., Baldo, B., Schnoegl, S., Kunz, S., Purfürst, B., Gaertner, A., Kampinga, H.H., Morton, A.J., Petersén, Å., Kirstein, J., Bates, G.P. and Wanker, E.E.
Abstract:Self-propagating, amyloidogenic mutant huntingtin (mHTT) aggregates may drive progression of Huntington's disease (HD). Here, we report the development of a FRET-based mHTT aggregate seeding (FRASE) assay that enables the quantification of mHTT seeding activity (HSA) in complex biosamples from HD patients and disease models. Application of the FRASE assay revealed HSA in brain homogenates of presymptomatic HD transgenic and knockin mice and its progressive increase with phenotypic changes, suggesting that HSA quantitatively tracks disease progression. Biochemical investigations of mouse brain homogenates demonstrated that small, rather than large, mHTT structures are responsible for the HSA measured in FRASE assays. Finally, we assessed the neurotoxicity of mHTT seeds in an inducible Drosophila model transgenic for HTTex1. We found a strong correlation between the HSA measured in adult neurons and the increased mortality of transgenic HD flies, indicating that FRASE assays detect disease-relevant, neurotoxic, mHTT structures with severe phenotypic consequences in vivo.
Keywords:Huntington's Disease, FRASE Assay, Mutant HTT Seeding, Huntingtin, Proteotoxicity, Seeding Activity, Disease Marker, Self-Propagation, HSA, Animals, Caenorhabditis elegans, Drosophila, Mice
Source:Molecular Cell
ISSN:1097-2765
Publisher:Elsevier / Cell Press
Volume:71
Number:5
Page Range:675-688
Date:6 September 2018
Additional Information:Copyright © 2018. This manuscript version is made available under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Official Publication:https://doi.org/10.1016/j.molcel.2018.07.032
PubMed:View item in PubMed

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