Misfolded protein aggregates represent a continuum with overlapping features in neurodegenerative diseases, but differences in protein components and affected brain regions. The molecular hallmark of synucleinopathies such as Parkinson's disease, dementia with Lewy bodies and multiple system atrophy are megadalton α-synuclein-rich deposits suggestive of one molecular event causing distinct disease phenotypes. Glial α-synuclein (α-SYN) filamentous deposits are prominent in multiple system atrophy and neuronal α-SYN inclusions are found in Parkinson's disease and dementia with Lewy bodies. The discovery of α-SYN assemblies with different structural characteristics or 'strains' has led to the hypothesis that strains could account for the different clinico-pathological traits within synucleinopathies. In this study we show that α-SYN strain conformation and seeding propensity lead to distinct histopathological and behavioural phenotypes. We assess the properties of structurally well-defined α-SYN assemblies (oligomers, ribbons and fibrils) after injection in rat brain. We prove that α-SYN strains amplify in vivo. Fibrils seem to be the major toxic strain, resulting in progressive motor impairment and cell death, whereas ribbons cause a distinct histopathological phenotype displaying Parkinson's disease and multiple system atrophy traits. Additionally, we show that α-SYN assemblies cross the blood-brain barrier and distribute to the central nervous system after intravenous injection. Our results demonstrate that distinct α-SYN strains display differential seeding capacities, inducing strain-specific pathology and neurotoxic phenotypes.

(2) and London mutation(s) (3) alter APP processing, causing increased production of the A␤ peptide of 42 amino acids (4), hypothesized to be pivotal in AD pathology (1, 5). Early onset familial AD caused by mutations in the presenilin genes supports this hypothesis, because they increase production of A␤ (42) peptide (6, 7) due to the gain of an unknown function (8). The extensive cell biological definition of the metabolic effects of the different mutations in APP in vitro requires matching analysis of their physiological impact in vivo. Transgenic mice with wild type and different mutant forms of APP have been generated and the original, most wanted end point, i.e. AD-like amyloid plaques in mouse brain, was obtained (9, 10), accompanied by cognitive deficits (11) and by hyperphosphorylation of protein tau (12). In other transgenic mouse strains overexpression of APP caused behavioral, synaptotrophic, and neurodegenerative effects, accelerated senescence, and premature death, in the absence of amyloid deposits (13-16). Intracellular expression of the A␤ peptide yielded mice with extensive neuronal loss but no amyloidosis (17). Overexpression of the C-terminal domain of APP caused neuronal degeneration (18), whereas in another model, pre-amyloid deposits, hippocampal cell loss, and cognitive deficits were documented (19).We have generated additional transgenic mouse strains, expressing human APP, either wild type or the London or Swedish clinical mutations, from the neuron-specific mouse thy-1 gene promoter. Their phenotype was analyzed by biochemical, histochemical, behavioral, electrophysiological, and pharmacological methods. Measurements of different APP metabolites in brain demonstrated that increased A␤(42) levels correlated with the formation of amyloid plaques in the brain of old APP/London transgenic mice. The plaques were extensively characterized immunohistochemically and displayed many aspects typically observed in the brain of AD patients. As opposed to plaques that developed only after at least 12 months of age, other deficits were observed from 3 months onwards and included cognitive impairment, decreased long term potentiation, differential glutamatergic responses, aggression, and neophobia, among others. These signs were largely independent of the actual isoform or mutant of APP that was expressed, were not correlated with a single APP metabolite, and are dissociated in time from plaque formation. These mice will be good models to study both early and late, neuropathological, and clinical aspects related to Alzheimer's disease. EXPERIMENTAL PROCEDURESGeneration of Transgenic Mice-cDNA coding for human wild type APP (695 isoform), the Swedish (K670N,M671L) mutant (770 isoform), and the London (V642I) mutant (695 isoform) were cloned in the pTSC vector in the mouse thy-1 gene (16). The purified, linearized minigenes were microinjected into prenuclear embryos from superovulated FVB/N females.Antibodies-Rabbit antisera B11/4 and B12/4, generated against a *

Mutations in the human tau gene cause frontotemporal dementia and parkinsonism linked to chromosome 17. Some mutations, including mutations in intron 10, induce increased levels of the functionally normal four-repeat tau protein isoform, leading to neurodegeneration. We generated transgenic mice that overexpress the four-repeat human tau protein isoform specifically in neurons. The transgenic mice developed axonal degeneration in brain and spinal cord. In the model, axonal dilations with accumulation of neurofilaments, mitochondria, and vesicles were documented. The axonopathy and the accompanying dysfunctional sensorimotor capacities were transgene-dosage related. These findings proved that merely increasing the concentration of the four-repeat tau protein isoform is sufficient to injure neurons in the central nervous system, without formation of intraneuronal neurofibrillary tangles. Evidence for astrogliosis and ubiquitination of accumulated proteins in the dilated part of the axon supported this conclusion. This transgenic model, overexpressing the longest isoform of human tau protein, recapitulates features of known neurodegenerative diseases, including Alzheimer's disease and other tauopathies. The model makes it possible to study the interaction with additional factors, to be incorporated genetically, or with other biological triggers that are implicated in neurodegeneration.

Protein tau filaments in brain of patients suffering from Alzheimer's disease, frontotemporal dementia, and other tauopathies consist of protein tau that is hyperphosphorylated. The responsible kinases operating in vivo in neurons still need to be identified. Here we demonstrate that glycogen synthase kinase-3␤ (GSK-3␤) is an effective kinase for protein tau in cerebral neurons in vivo in adult GSK-3␤ and GSK-3␤ ؋ human tau40 transgenic mice. Phosphorylated protein tau migrates slower during electrophoretic separation and is revealed by phosphorylation-dependent anti-tau antibodies in Western blot analysis. In addition, its capacity to bind to re-assembled paclitaxel (Taxol ® )-stabilized microtubules is reduced, compared with protein tau isolated from mice not overexpressing GSK-3␤. Co-expression of GSK-3␤ reduces the number of axonal dilations and alleviates the motoric impairment that was typical for single htau40 transgenic animals (Spittaels, K., Van den Haute, C., Van Dorpe, J., Bruynseels, K., Vandezande, K., Laenen, I., Geerts, H., Mercken, M., Sciot, R., Van Lommel, A., Loos, R., and Van Leuven, F. (1999) Am. J. Pathol. 155, 2153-2165). Although more hyperphosphorylated protein tau is available, neither an increase in insoluble protein tau aggregates nor the presence of paired helical filaments or tangles was observed. These findings could have therapeutic implications in the field of neurodegeneration, as discussed.