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Effects of humanized exon 10 splicing in murine tau on pathological phenotypes in tg-ArcSwe mice
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Public Health and Caring Sciences. (Molecular Geriatrics)
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Public Health and Caring Sciences. (Molecular Geriatrics)
Department of Pharmacology, Oslo University and Oslo University Hospital, Norway.
(English)Manuscript (preprint) (Other academic)
Keyword [en]
Alzheimer's disease, Alternative splicing, amyloid deposition, bitransgenic mice, Microtubule, Tau
National Category
Neurosciences Cell and Molecular Biology
URN: urn:nbn:se:uu:diva-222767OAI: oai:DiVA.org:uu-222767DiVA: diva2:712755
Available from: 2014-04-16 Created: 2014-04-14 Last updated: 2014-06-30
In thesis
1. Therapeutic and functional studies in animal models of Alzheimer's disease
Open this publication in new window or tab >>Therapeutic and functional studies in animal models of Alzheimer's disease
2014 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Senile plaques (Aβ) and neurofibrillary tangles (tau) are pathological hallmarks of Alzheimer’s disease (AD). If and how the formation of these deposits are mechanistically linked remains mainly unknown. In recent years, the focus has shifted from insoluble protein deposits to soluble aggregates of Aβ and tau. Protofibrils are large soluble Aβ oligomers which were linked to AD by the discovery of the Arctic AβPP mutation.

Treatment of young tg-ArcSwe mice with an Aβ protofibril-selective antibody, mAb158, cleared protofibrils, prevented amyloid plaque deposition and protected cultured cells from protofibril-mediated toxicity. This suggests that Aβ protofibrils are necessary for the formation of Aβ deposits. Functional assessment of tg-ArcSwe mice in IntelliCage demonstrated hippocampal-dependent behavioral deficits such as memory/learning impairments, hyperactivity and perseverance behavior. Learning impairments did not correlate to Aβ-measures but to calbindin, which might be a good marker for Aβ-mediated neuronal dysfunction.

Splicing of exon 10 in the tau gene differs between human and mouse brain. Exon 10 is part of the microtubule-binding domains which helps to maintain microtubule stability and axonal transport, functions vital to neuronal viability. Axonal transport dysfunction has been proposed as a common pathway of Aβ and tau pathogenesis in AD. Generation of a novel tau mouse model with absence of exon 10 led to age-dependent sensorimotor impairments which may relate to dysfunctions in cerebellum. No tau pathology was evident suggesting that a trigger of tau fibrillization e.g. a human Aβ or tau aggregate is needed. Generation of AβPPxE10 bitransgenic mice with no exon 10 showed lower Aβ plaque burden. Possibly changes in microtubule function lead to altered intracellular AβPP transport and Aβ production. Initiation of tau pathology in AβPPxE10 mice might require a certain type of Aβ-aggregates which is not produced or exist at too low concentration in transgenic mouse brain.

In summary, the Aβ protofibril-selective antibody was found to be a promising treatment for AD. The IntelliCage system was proven to be useful for functional evaluation of AβPP mice. Exon 10 in tau was shown to affect sensorimotor functions and Aβ pathology in bitransgenic mice by mechanisms that deserve further investigation.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2014. 73 p.
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 1003
Alzheimer's disease, Amyloid-beta, Immunotherapy, IntelliCage, Microtubule, Tau, Alternative splicing
National Category
Neurosciences Microbiology in the medical area
Research subject
Neuroscience; Medical Cell Biology; Medical Biochemistry
urn:nbn:se:uu:diva-223135 (URN)978-91-554-8961-8 (ISBN)
Public defence
2014-06-12, Rudbecksalen, Rudbecklaboratoriet, Dag Hammarskjölds väg 20, Uppsala, 09:15 (English)
Available from: 2014-05-22 Created: 2014-04-16 Last updated: 2014-09-18Bibliographically approved

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