Claims for Patent: 6,717,031

Summary for Patent: 6,717,031

Title:	Method for selecting a transgenic mouse model of alzheimer\'s disease
Abstract:	The construction of transgenic animal models of human Alzheimer\'s disease, and methods of using the models to screen potential Alzheimer\'s disease therapeutics, are described. The models are characterized by pathologies similar to pathologies observed in Alzheimer\'s disease, based on expression of all three forms of the .beta.-amyloid precursor protein (APP), APP695, APP751, and APP770, as well as various point mutations based on naturally occurring mutations, such as the London and Indiana familial Alzheimer\'s disease (FAD) mutations at amino acid 717, predicted mutations in the APP gene, and truncated forms of APP that contain the A.beta. region. Animal cells can be isolated from the transgenic animals or prepared using the same constructs with standard techniques such as lipofection or electroporation. The transgenic animals, or animal cells, are used to screen for compounds altering the pathological course of Alzheimer\'s disease as measured by their effect on the amount of APP, .beta.-amyloid peptide, and numerous other Alzheimer\'s disease markers in the animals, the neuropathology of the animals, as well as by behavioral alterations in the animals.
Inventor(s):	Games; Kate Dora (San Francisco, CA), Schenk; Dale Bernard (Pacifica, CA), McConlogue; Lisa Claire (San Francisco, CA), Seubert; Peter Andrew (S. San Francisco, CA), Rydel; Russell E. (Belmont, CA)
Assignee:
Application Number:	09/149,718
Patent Claims:	1. A method of selecting a transgenic mouse as a model of Alzheimer's disease, comprising providing a plurality of transgenic mice, each comprising a nucleic acid construct stably incorporated into the genome, wherein the construct comprises a promoter for expression of the construct in a mammalian cell and a region encoding an Au-containing protein, wherein the promoter is operatively linked to the region, wherein the region comprises DNA encoding the A.beta.-containing protein, wherein the A.beta.-containing protein consists of all or a contiguous portion of a protein selected from the group consisting of APP770 bearing a mutation in one or more of the amino acids selected from the a group consisting of amino acid 669, 670, 671, 690, 692, and 717, APP751 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, and APP695 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717; a protein consisting of amino acids 672 to 770 of APP; and a protein consisting of amino acids 672 to 714 of APP; determining expression levels of APP, APP.beta., APP.alpha. and/or A.beta. in each of the transgenic mice; identifying a transgenic mouse wherein A.beta.tot is expressed at a level of at least 30 nanograms per gram of brain tissue of the mouse when it is two to four months old, A.beta.1-42 is expressed at a level of at least 8.5 nanograms per gram of brain tissue of the mouse when it is two to four months old, APP and APP.alpha. combined are expressed at a level of a least 150 picomoles per gram of brain tissue of the mouse when it is two to four months old, APP.beta. is expressed at a level of at least 40 picomoles per gram of brain tissue of the mouse when it is two to four months old, and/or mRNA encoding the A.beta.-containing protein is expressed to a level at least twice that of mRNA encoding the cndogenous APP of the transgenic mouse in brain tissue of the mouse when it is two to four months old; using an offspring of the identified transgenic mouse as a model of Alzheimer's disease. 2. The method of claim 1, further comprising administering a compound to be tested to the offspring or cells drived therefrom, and detecting or measuring the Alzheimer's disease marker such that any difference between the marker in the transgenic mouse, or by cells derived from the transgenic mouse rodent, and the marker in a transgenic mouse to which the compound has not been administered, or by cells derived from the transgenic mouse to which the compound has not been administered, is observed, wherein an observed difference in the marker indicates that the compound has an effect on the marker. 3. The method of claim 2 wherein the Alzheimer's disease marker is a protein and the observed difference is an increase or decrease in the amount of the protein present in the transgemc mouse to which the compound has been administered, or by cells derived from the transgenic mouse to which the compound has been administered. 4. The method of claim 3 wherein the protein is selected from the group consisting of Cat D,B, Neuronal Thread Protein, nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, synaptophysin, p65, glutamine synthetase, glucose transporter, PPI kinase, GAP43, cytochrome oxidase, heme oxygenase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1.alpha., IL-1.beta., TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, tau, ubiquitin, MAP-2, apolipoprotein E, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), advanced glycosylation end products, receptor for advanced glycosylation end products, COX-2, CD18, C3, fibroblast growth factor, CD44, ICAM-1, lactotransferrin, C1q, C3d, C4d, C5b-9, gamma RI, Fc gamma RII, CD8, CD59, vitronectin, vitronectin receptor, beta-3 integrin, Apo J, clusterin, type 2 plasminogen activator inhibitor, midkine, macrophage colony stimulating factor receptor, MRP14, 27E10, interferon-alpha, S100.beta., cPLA.sub.2, c-jun, c-fos, HSP27, HSP70, MAP5, membrane lipid peroxidase, protein carbonyl formation, junB, jund, fosB, fra1, cyclin D1, p53, NGFI-A, NGFI-B, I.kappa.B, NF.kappa.B, IL-8, MCP-1, MIP-1.alpha., matrix metaloproteinases, 4-hydroxynonenal-protein conjugates, amyloid P component, laminin, and collagen type IV. 5. The method of claim 3 wherein the Alzheimer's disease marker is selected from the group consisting of A.beta..sub.tot, A.beta..sub.1-42, A.beta..sub.1-40, A.beta..sub.N3 (pE), A.beta..sub.X-42, A.beta..sub.X-40, A.beta..sub.Insoluble, A.beta..sub.Soluble, full length APP, APP.alpha., APP.beta., FLAPP+ APP.alpha., the last 100 amino acids of APP, and the last 57 to 60 amino acids of APP. 6. The method of claim 2 wherein the Aizheimer's disease marker is a protein and the observed difference is a reduction or absence of the protein in plaques or neuritic tissue present in the transgenic mouse to which the compound has been administered. 7. The method of claim 6 wherein the protein is selected from the group consisting of Cat D,B, protein kinase C, NADPH, C3d, C1q, C5, C4bp, C5a-C9, tau, ubiquitin, MAP-2, neurofilaments, heparin sulfate, chrondroitin sulphate, apolipoprotein E, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glycosylation end products, amyloid P component, laminin, and collagen type IV. 8. The method of claim 2 wherein the Alzheimer's disease marker is a protein and the observed difference is an increase or decrease in the enzymatic or biochemical activity of the protein in the transgenic mouse to which the compound has been administered, or by cells derived from the transgenic mouse to which the compound has been administered. 9. The method of claim 8 wherein the protein is selected from the group consisting of nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, glutamine synthetase, glucose transporter, PPI kinase, cytochrome oxidase, heme oxygenase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1, TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, ubiquitin, and apolipoprotein E. 10. The method of claim 2 wherein the Alzheimer's disease marker is a nucleic acid encoding a protein and the observed difference is an increase or decrease in the amount of the nucleic acid present in the transgenic mouse to which the compound has been administered, or by cells derived from the transgenic mouse to which the compound has been administered. 11. The method of claim 10 wherein the encoded protein is selected from the group consisting of growth inhibitory factor, Cat D,B, Neuronal Thread Protein, nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, synaptophysin, p65, glutamine synthetase, glucose transporter, PPI kinase, GAP43, cytochrome oxidase, heme oxygenase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1, TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, tau, ubiquitin, MAP-2, apolipoprotein E, nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), advanced glycosylation end products, receptor for advanced glycosylation end products, COX-2, CD18, C3, fibroblast growth factor, CD44, ICAM-1, lactotransferrin, C1q, C3d, C4d, C5b-9, gamma RI, Fc gamma RII, CD8, CD59, vitronectin, vitronectin receptor, beta-3 integrin, Apo J, clusterin, type 2 plasminogen activator inhibitor, midkine, macrophage colony stimulating factor receptor, MRP14, 27E10, interferon-alpha, S100.beta., cPLA.sub.2, c-jun, c-fos, HSP27, HSP70, MAP5, membrane lipid peroxidase, protein carbonyl formation, junB, junD, fosB, fra1, cyclin D1, p53, NGFI-A, NGFI-B, I.kappa.B, NF.kappa.B, IL-8, MCP-1, MIP-1.alpha., matrix metaloproteinases, 4-hydroxynonenal-protein conjugates, amyloid P component, laminin, and collagen type IV. 12. The method of claim 2 wherein the Alzheimer's disease marker is a behavior and the observed difference is a change in the behavior observed in the transgenic mouse to which the compound has been administered. 13. The method of claim 12 wherein the behavior is selected from the group consisting of behavior using working memory, behavior using reference memory, locomotor activity, emotional reactivity to a novel environment or to novel objects, and object recognition. 14. The method of claim 2 wherein the Alzheimer's disease marker is a histopathology and the observed difference is a decrease in the extent or severity of the histopathology present in the transgenic mouse to which the compound has been administered. 15. The method of claim 14 wherein the histopathology marker is selected from the group consisting of compacted plaques, neuritic dystrophy, gliosis, A.beta. deposits, decreased synaptic density, and neuropil abnormalities. 16. The method of claim 14 wherein the Alzheimer's disease marker is selected from the group consisting of APP695, APP751, and APP770, and wherein the change in histopathology is a reduction in the amount of Alzheimer's disease marker localized in plaques and neuritic tissue. 17. The method of claim 16 wherein the intron is an APP gene intron. 18. The method of claim 2 wherein the Alzheimer's disease marker is cognition and the observed difference is a change in the cognition of the transgenic mouse to which the compound has been administered. 19. The method of claim 2 wherein the marker is detected or measured using RT-PCR, RNase protection, Northern analysis, R-dot analysis, ELISA, antibody staining, laser scarming confocal imaging, and immunoelectron micrography. 20. The method of claim 2 wherein the codon encoding amino acid 717 is mutated to encode an amino acid selected from the group consisting of Ile, Phe, Gly, Tyr, Leu, Ala, Pro, Trp, Met, Ser, Thr, Mn, and Gln. 21. The method of claim 20 wherein the codon encoding amino acid 717 is mutated to encode Phe. 22. The method of claim 2 wherein the codon encoding amino acid 670 is mutated to encode an amino acid selected from the group consisting of Asn and Glu, or the codon encoding amino acid 670 is deleted, and/or wherein the codon encoding amino acid 671 is mutated to encode an amino acid selected from the group consisting of Ile, Leu, Tyr, Lys, Glu, Val, and Ala, or the codon encoding amino acid 671 is deleted. 23. The method of claim 22 wherein the codon encoding amino acid 670 is mutated to encode Asn, and/or the codon encoding amino acid 671 is mutated to encode Leu or Tyr. 24. The method of claim 2 wherein the promoter mediates expression of the construct such that A.beta..sub.tot is expressed at a level of at least 30 nanograms per gram of hippocampal or cortical brain tissue of the mouse when it is two to four months old, A.beta.1-42 is expressed at a level of at least 8.5 nanograms per gram of hippocampal or cortical brain tissue of the mouse when it is two to four months old, APP and APP.alpha. combined are expressed at a level of at least 150 picomoles per gram of hippocampal or cortical brain tissue of the mouse when it is two to four months old, APP.beta. is expressed at a level of at least 40 picomoles per gram of hippocampal or cortical brain tissue of the mouse when it is two to four months old, and/or mRNA encoding the A.beta.-containing protein is expressed to a level at least twice that of mRNA encoding the endogenous APP of the transgenic mouse in hippocampal or cortical brain tissue of the mouse when it is two to four months old. 25. The method of claim 1, wherein the A.beta.-containing protein consists of all or a contiguous portion of a protein selected from the group consisting of APP770 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, APP751 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, and APP695 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717. 26. The method of claim 25 wherein the region of the construct encoding a human amnyloid precursor protein is selected from the group consisting of APP770 cDNA bearing a mutation in the codon encoding amino acid 669, 670, 671, 690, 692, 717, or a combination of these mutations; APP751 cDNA bearing a mutation in the codon encoding amino acid 669, 670, 671, 690, 692, 717, or a combination of these mutations; the APP695 cDNA bearing a mutation in the codon encoding amino acid 669, 670, 671, 690, 692, 717, or a combination of these mutations; APP695, APP751, or APP770 cDNA truncated at amino acid 671 or 685; APP cDNA truncated to encode amino acids 646 to 770 of APP; a combination cDNA/genomic APP gene construct bearing a mutation in the codon encoding amino acid 669, 670, 671, 690, 692, 717, or a combination of these mutations; and a combination cDNA/genomic APP gene construct truncated at amino acid 671 or 685. 27. The method of claim 1 wherein the DNA encoding the A.beta.-containing protein is cDNA or a cDNA/genomjc DNA hybrid, wherein the cDNA/genomic DNA hybrid includes at least one APP intron sequence wherein the intron sequence is sufficient for splicing. 28. The method of claim 1 wherein the promoter is the human platelet derived growth factor .beta. chain gene promoter. 29. The method of claim 1 wherein the region further comprises DNA encoding a second protein, wherein the DNA encoding the A.beta.-containing protein and the DNA encoding the second protein are operative linked such that the region encodes an A.beta.-containing fusion protein comprising a fusion of the A.beta.-containing protein and the second protein. 30. The method of claim 29 wherein the second protein is a signal peptide. 31. The method of claim 1 wherein the construct further comprises an effective amount of at least one intron, wherein the effective amount of at least one intron is located in the region of the construct encoding the A.beta.-containing protein. 32. The method of claim 1 wherein the A.beta.-containing protein consists of all or a contiguous portion of a protein selected from the group consisting APP770 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, APP751 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, and APP695 bearing a mutation in one or more of the ammo acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717. 33. A method of selecting a transgenic mouse ha a model of Aizheimer's disease, comprising providing a plurality of transgenic mice, each comprising a nucleic acid construct stably incorporated into the genome, wherein the construct comprises a promoter for expression of the construct in a mammalian cell and a region encoding an A.beta.-containing protein, wherein the promoter is operatively linked to the region, wherein the region comprises DNA encoding the A.beta.-containing protein, wherein the A.beta.-containing protein consists of all or a contiguous portion of a protein selected from the group consisting of APP770 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, APP751 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 717, and APP695 bearing a mutation in one or more of the amino acids selected from the group consisting of amino acid 669, 670, 671, 690, 692, and 711, a protein consisting of amino acids 672 to 770 of APP; and a protein consisting of amino acids 672 to 714 of APP; determining expression levels of A.beta. and Congo red staining in the brains of each of the transgenic mice; identifying a transgenic mouse; wherein A.beta. is expressed at a level of at least 50 ng/g brain tissue in the identified transgenic mouse when the transgenic mouse is three months of age; and using an offspring of the identical transgenic mouse as a model of Alzheimer's Disease. 34. The method of claim 33, further comprising administering a compound to be tested to the offspring or cells derived therefrom, and detecting or measuring the Alzheimer's disease marker such that any difference between the marker in the transgenic mouse, or by cells derived from the transgenic mouse rodent, and the marker in a transgenic mouse to which the compound has not been administered, or by cells derived from the transgenic mouse to which the compound has not been administered, is observed, wherein an observed difference in the marker indicates that the compound has an effect on the marker. 35. The method of claim 33 wherein the Alzheimer's disease marker is a protein and the observed difference is an increase or decrease in the amount of the protein present in the transgenic mouse to which the compound has been administered, or in cells derived from the transgenic mouse to which the compound has been administered. 36. The method of claim 35 wherein the protein is selected from the group consisting of Cat D,B, Neuronal Thread Protein (CSF), nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, synaptophysin, p65, glutarnine synthetase, glucose transporter, PPI kinase, GAP43, cytochrome oxidase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antichymotrypsin, .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1, TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, tau, ubiquitin, MAP-2, apolipoprotein E, glycosylation end products, amyloid P component, laminen, and collagen type IV. 37. The method of claim 33 wherein the Alzheimer's disease marker is a protein and the observed difference is a reduction or absence of the protein in plaques or neuritic tissue present in the transgenic mouse to which the compound has been administered. 38. The method of claim 37 wherein the protein is selected from the group consisting of Cat D,B, protein kinase C, NADPH, C3d, C1q, CS, C4bp, C5a-C9, tau, ubiquitin, MAP-2, neurofilaments, heparin sulfate, chrondroitin sulphate, apolipoprotein E, glycosylation end products, amyloid P component, laminen, and collagen type IV. 39. The method of claim 33 wherein the Alzheimer's disease marker is a protein and the observed difference is an increase or decrease in the enzymatic or biochemical activity of the protein in the fransgenic mouse to which the compound has been administered, or in cells derived from the transgenic mouse to which the compound has been administered. 40. The method of claim 39 wherein the protein is selected from the group consisting of nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, glutamine synthetase, glucose transporter, PPI kinase, cytochrome oxidase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antichymotrypsin, .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1, TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, ubiquitin, and apolipoprotein E. 41. The method of claim 33 wherein the Alzheimer's disease marker is a nucleic acid encoding a protein and the observed difference is an increase or decrease in the amount of the nucleic acid present in the transgenic mouse to which the compound has been administered, or in cells derived from the transgenic mouse to which the compound has been administered. 42. The method of claim 41 wherein the protein is selected from the group consisting of growth inhibitory factor, Cat D,B, Neuronal Thread Protein (CSF), nicotine receptors, 5-HT.sub.2 receptor, NMDA receptor, .alpha.2-adrenergic receptor, synaptophysin, p65, glutamine synthetase, glucose transporter, PPI kinase, GAP43, cytochrome oxidase, calbindin, adenosine A1 receptors, choline acetyltransferase, acetylcholinesterase, glial fibrillary acidic protein (GFAP), .alpha.1-antichymotrypsin, .alpha.1-antitrypsin, C-reactive protein, .alpha.2-macroglobulin, IL-1, TNF.alpha., IL-6, HLA-DR, HLA-A, D,C, CR3 receptor, MHC I, MHC II, CD 31, CR4, CD45, CD64, CD4, spectrin, tall, ubiquitin, MAP-2, apolipoprotein E, glycosylation end products, amyloid P component, laminen, and collagen type IV. 43. The method of claim 33 wherein the Alzheimer's disease marker is a behavior and the observed difference is a change in the behavior observed in the transgenic mouse to which the compound has been administered. 44. The method of claim 43 wherein the behavior is selected from the group consisting of behavior using working memory, behavior using reference memory, locomotor activity, emotional reactivity to a novel environment or to novel objects, and object recognition. 45. The method of claim 33 wherein the Alzheimer's disease marker is a histopatbology and the observed difference is a decrease in the extent or severity of the histopathology present in the transgenic mouse to which the compound has been administered. 46. The method of claim 45 wherein the histopathology is selected from the group consisting of compacted plaques, neuritic dystrophy, gliosis, A,.beta. deposits, decreased synaptic and neuropil abnormalities. 47. The method of of claim 45 wherein the Alzheimer's disease marker is selected from the group consisting of APP695, APP751, and APP770, and wherein the change in histopathology is a reduction in the amount of the marker localized in plaques and neuritic tissue. 48. The method of claim 33 wherein the Alzheimer's disease marker is cognition and the observed difference is a change in the cognition of the transgenic mouse to which the compound has been administered. 49. The method of claim 33 wherein the marker is detected or measured using RT-PCR, ELISA, antibody staining, laser scanning confocal imaging, and immunoelectron micrography. 50. The method of claim 33 wherein the codon encoding amino acid 717 is mutated to encode an amino acid selected from the group consisting of Ile, Phe, Gly, Tyr, Leu, Ala, Pro, Tip, Met, Ser, Thr, Asn, and Gin. 51. The method of claim 50 wherein the codon encoding amino acid 717 is mutated to encode Phe. 52. The method of claim 33 wherein the codon encoding amino acid 670 is mutated to encode an amino acid selected from the group consisting of Asn and Glu, or the codon encoding amino acid 670 is deleted, and wherein the codon encoding amino acid 671 is mutated to encode an amino acid selected from the group consisting of Ile, Lys, Glu, Val, and Ala, or the codon encoding amino acid 671 is deleted. 53. The method of claim 52 wherein the codon encoding amino acid 670 is mutated to encode Asn, and the codon encoding amino acid 671 is mutated to encode Leu. 54. The method of claim 33 wherein the Alzheimer's disease marker is selected from the group consisting of A.beta..sub.tot, A.beta..sub.1-42, A.beta..sub.N3 (pE), A.beta..sub.x-42, and A.beta..sub.Insoluble. 55. The method of claim 33 wherein the construct further comprises an effective amount of at least one intron, wherein the effective amount of at least one intron is located in the region of the construct encoding a human amyloid precursor protein. 56. The method of claim 55 wherein the intron is an APP gene intron.

Details for Patent 6,717,031

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2015-06-07
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2015-06-07
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2015-06-07