Alzheimer's disease animal model
AssigneesInserm (Institut National De La Sante Et De La Recherche Medicale), Universite de Paris-sud, Commissariat A L'energie Atomique Et Aux Energies Alternatives, Centre National de la Recherche Scientifique (CNRS), Universite Paris Descartes
InventorsNathalie Cartier-Lacave, Jerome Braudeau, Nicole Deglon, Philippe Hantraye, Mickael Audrain
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Abstract
The present invention relates to a vector comprising a nucleic acid sequence that encodes the APP protein and/or the PS1 protein or variants thereof. The invention also relates to a method for inducing the Alzheimer's disease in an animal using the vector of the invention and to animal model having the Alzheimer's disease obtained by said method.
Claims18
A method for inducing aspects of Alzheimer's disease in a non-human mammal, said method consisting of co-administering to the brain of the non-human mammal, a nucleic acid sequence encoding Amyloid Precursor Protein (APP) or a variant thereof and a nucleic acid sequence encoding Presenilin 1 (PS1) protein or a variant thereof,
- wherein the nucleic acid sequence encoding the APP protein or a variant thereof and the nucleic acid sequence encoding PS1 protein or a variant thereof are present in at least one vector, and wherein only the APP protein or the variant thereof and the PS1 protein or the variant thereof are co-expressible from the at least one vector;
- and
- wherein co-expression of said APP or the variant thereof and said PS1 or the variant thereof in the brain of the non-human mammal results in the non-human mammal exhibiting behavior suggestive of anxiety and lack of long-term memory;
- and
- wherein co-expression of said APP or the variant thereof and said PS1 or the variant thereof in the brain of the non-human mammal leads to production of βAPP and neurotoxic catabolites of βAPP from one month after administration and up until at least 12 months after administration without the appearance of classical AD late symptoms.
A non-human mammal having symptoms of Alzheimer's disease
- wherein the symptoms of Alzheimer's disease are induced by a method consisting of
- administering to the non-human mammal at least one vector containing a nucleic acid sequence that encodes an APP protein or a variant thereof and a nucleic acid sequence that encodes a PS1 protein or a variant thereof, and wherein only the APP protein or the variant thereof and the PS1 protein or the variant thereof are co-expressible from the at least one vector,
- wherein co-expression of said APP or the variant thereof and said PS1 or the variant thereof in the brain of the non-human mammal results in the non-human mammal exhibiting behavior suggestive of anxiety and lack of long-term memory;
- and
- wherein co-expression of said APP or the variant thereof and said PS1 or the variant thereof in the brain of the non-human mammal leads to production of βAPP and neurotoxic catabolites of βAPP from one month after administration and up until at least 12 months after administration without the appearance of classical AD late symptoms.
Dependencies are inferred from the claim text.