Transmission of human prion diseases to rodents

Seminars in Virology

Volumn 7, Issue 3, 1996, Pages 175-180

  Tateishi, Jun ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

Creutzfeldt Jakob disease; Gerstmann Straussler Scheinker syndrome; Prions; Rodent; Transmission

Indexed keywords

ADULT; AGED; ALZHEIMER DISEASE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; CLINICAL ARTICLE; CODON; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DISEASE COURSE; DISEASE TRANSMISSION; DNA POLYMORPHISM; FEMALE; GENOTYPE; HUMAN; HUMAN TISSUE; MALE; MOUSE; NONHUMAN; PHENOTYPE; PRION DISEASE; RAT; REVIEW; SYNAPSE;

ANIMALIA; RODENTIA;

EID: 0030007616     PISSN: 10445773     EISSN: None     Source Type: Journal    
DOI: 10.1006/smvy.1996.0022     Document Type: Review

References (43)

1. Gajdusek DC, Gibbs CJ Jr, Alpers M (1967) Transmission and passage of experimental 'kuru' to chimpanzees. Science 155:212-214
2. Gibbs CJ Jr, Gajdusek DC, Asher DM, Alpers MP, Beck E, Daniel PM, Matthews WB (1968) Cruetzfeldt-Jakob disease (spongi-form encephalopathy); Transmission to the chimpanzee. Science 161:388-389
3. Manuelidis EE, Manuelidis L (1979) Clinical and morphological aspects of transmissible Creutzfeldt-Jakob disease, in Progress in Neuropathology (Zimmerman HM, ed.) Vol 4, pp 1-26. Raven Press, New York
4. Tateishi J, Sato Y, Ohta M (1983) Creutzfeldt-Jakob disease in humans and laboratory animals, in Progress in Neuropathology (Zimmerman HM, ed.) Vol 5, pp 195-221. Raven Press, New York
5. Tateishi J, Hikita K, Kitamoto T, Nagara H (1987) Experimental Creutzfeldt-Jakob disease: induction of amyloid plaques in rodents, in Prions. Novel infectious pathogens causing scrapie and Creutzfeldt-Jakob disease (Prusiner SB, MaKinley MP, eds) pp 415-426. Academic Press, San Diego
6. Prusiner SB (1991) Molecular biology of prion disease. Science 252:1515-1522
7. Tateishi J (1985) Transmission of Creutzfeldt-Jakob disease from human blood and urine into mice. Lancet 2:1074 (Letter)
8. Muramoto T, Kitamoto T, Hoque MZ, Tateishi J, Goto I (1993) Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease. J Virol 67:6808-6810
9. Hsiao K, Baker HF, Crow TJ, Poulter M, Owen F, Terwilliger JD, Westaway D, Otto JP, Prusiner SB (1989) Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome. Nature 338:342-345
10. Doh-ura K, Tateishi J, Sasaki H, Kitamoto T, Sakaki Y (1989) Pro→Leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. Biochem Biophys Res Commun 163:974-979
11. Kitamoto T, Shin R-W, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J (1992) Abnormal isoform of prion protein accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 140:1285-1294
12. Gerstmann J, Sträussler E, Scheinker J (1936) Über eine eigenartige hereditär-familiäre Erkrankung des Zentralnervensystems. Z Neurol 154:736-762
13. Gasset M, Baldwin MA, Lloyd G, Gabriel J-M, Holtzmann DM, Cohen F, Fletterick R, Prusiner SB (1992) Predicted α-helical regions of the prion protein when synthesized as peptides form amyloid. Proc Natl Acad Sci USA 89:10940-10944
14. DeArmond SJ, Prusiner SB (1995) Etiology and pathogenesis of prion diseases. Am J Pathol 146:785-811
15. Tateishi J, Kitamoto T (1995) Inherited prion diseases and transmission to rodents. Brain Pathol 5:53-59
16. Doh-ura K, Kitamoto T, Sakaki Y, Tateishi J (1991) CJD discrepancy. Nature 353:801-802
17. Yamada S, Aiba T, Endo Y, Hara M, Kitamoto T, Tateishi J (1994) Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft. Neurosurgery 34:740-744
18. Uchiyama S, Ishida C, Yago S, Kurumaya H, Kitamoto T (1994) An autopsy case of Creutzfeldt-Jakob disease associated with corneal transplantation. Dementia 8:466-473 (in Japanese)
19. Kretzschmar HA, Honold G, Seitelberger F, Feucht M, Wessely P, Mehraein P, Budka H (1991) Prion protein mutation in family first reported by Gerstmann, Sträussler and Scheinker. Lancet 337:1160
20. Hainfellner JA, Brantner-Inthaler S, Cervenáková L, Brown P, Kitamoto T, Tateishi J, Diringer H, Liberski PP, Regele H, Feucht M, Mayr N, Wessely P, Summer K, Seitelberger F, Budka H (1995) The original Gerstmann-Sträussler-Scheinker family of Austria: Divergent clinicopathological phenotypes but constant PrP genotype. Brain Pathol 5:201-211
21. Tateishi J, Ohta M, Koga M, Sato Y, Kuroiwa Y (1979) Transmission of chronic spongiform encephalopathy with kuru plaques from human to small rodents. Ann Neurol 5:581-584
22. Tateishi J, Kitamoto T, Hashiguchi H, Shii H (1988) Gerstmann-Sträussler-Scheinker disease: Immunohistological and experimental studies. Ann Neurol 24:35-40
23. Kitamoto T, Tateishi J (1994) Human prion diseases with variant prion protein. Phil Trans R Soc Lond [Biol] 4:971-979
24. Tateishi J, Brown P, Kitamoto T, Hoque ZM, Roos R, Wollman R, Cervenáková L, Gajdusek DC (1995) First experimental transmission of fatal familial insomnia. Nature 376:434-435
25. Reder AT, Mednick AS, Brown P, Spire JP, Cauter EV, Wollmann RL, Cervenáková L, Goldfarb LG, Garay A, Ovsiew F, Gajdusek DC, Roos RP (1995) Clinical and genetic studies of fatal familial insomnia. Neurology 45:1068-1075
26. Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, Haltia M, Wills PR, Hauw JJ, McKeever PE, Monari L, Schrank B, Swergold GD, Autilio-Gambetti L, Gajdusek DC, Lugaresi E, Gambetti P (1992) Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Disease phenotype determined by a DNA polymorphism. Science 258:806-808
27. Vnencak-Jones CL, Phillips JA III (1992) Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH). Am J Hum Genet 50:871-872
28. Diedrich JF, Knopman DS, List JF, Olson K, Frey WH II, Emory CR, Sung JH, Haase AT (1992) Deletion in the prion protein gene in a demented patient. Human Mol Genet 1:443-444
29. Mizusawa H, Ohkoshi N, Sasaki H, Kanazawa I, Nakanishi T (1988) Degeneration of the thalamus and inferior olives associated with spongiform encephalopathy of the cerebral cortex. Clin Neuropathol 7:81-86
30. Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J (1994) Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein. Neurology 44:299-301
31. Brown P, Gibbs CJ Jr, Rodgers-Johnson P, Asher DM, Sulima MP, Bacote A, Goldfarb LG, Gajdusek DC (1994) Human spongi-form encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease. Ann Neurol 35:513-529
32. Tateishi J, Kitamoto T, Hoque MZ, Furukawa H (1996) Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents. Neurology 46: 532-537
33. Isozaki E, Miyamoto K, Kagamihara Y, Nagashima T, Hirose K, Tanabe H, Uchihara T, Oda M (1994) Creutzfeldt-Jakob disease presenting as frontal lobe dementia associated with a 96 base pair insertion in the prion protein gene. Dementia 8:363-371 (in Japanese)
34. Oda T, Kitamoto T, Tateishi J, Mitsuhashi T, Iwabuchi K, Haga C, Oguni E, Kato Y, Tominaga I, Yanai K, Kashima H, Kogure T, Hori K, Ogino K (1995) Prion disease with 144 base pair insertion in a Japanese family line. Acta Neuropathol 90:80-86
35. Mizushima S, Ishii K, Nishimaru T (1994) A case of presenile dementia with a 168 base pair insertion in prion protein gene. Dementia 8:830-390 (in Japanese)
36. Kitamoto T, Amano N, Terao Y, Nakazato Y, Issiki T, Mizutani T, Tateishi J (1993) A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis. Ann Neurol 34:808-813
37. Tranchant C, Doh-ura K, Warter JM, Steinmetz G, Chevalier Y, Hanauer A, Kitamoto T, Tateishi J (1992) Gerstmann-Sträussler-Scheinker disease in an Alsatian family: Clinical and genetic studies. J Neurol Neurosurg Psychiat 55:185-187
38. Kitamoto T, Iizuka R, Tateishi J (1993) An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques. Biochem Biophys Res Commun 192:525-531
39. Dlouhy SR, Hsiao K, Farlow MR, Foround T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B (1992) Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. Nature Genet 1:64-67
40. Iwabuchi K, Endoh S, Hagimoto H, Okamoto K, Miyakawa T, Yamaguchi T, Kajiwara A, Inoue K, Yamada Y, Amano N, Yagishita S (1994) Three patients from two families with familial Creutzfeldt-Jakob disease having a point mutation in the prion protein gene at codon 200 (Glu→Lys). Noshinkei 46:349-354 (in Japanese)
41. Pocchiari M, Salvatore M, Cutruzzolá F, Genuardi M, Alocatelli CT, Masullo C, Macchi G, Alemá G, Galgani S, Xi YG, Petraroli R, Silverstrini MC, Brunori M (1993) A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease. Ann Neurol 34:802-807
42. Hsiao K, Dlouhy SR, Farlow MR, Cass C, Costa MD, Conneally PM, Hodes ME, Ghetti B, Prusiner SB (1992) Mutant prion proteins in Gerstmann-Stráussler-Scheinker disease with neurofibrillary tangles. Nature Genet 1:68-71
43. Muramoto T, Kitamoto T, Koga H, Tateishi J (1992) The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration. Acta Neuropathol 84:686-689