Les agents transmissibles non conventionnels ou prions

Virologie

Volumn 1, Issue 1, 1997, Pages 11-22

  Dormont, D ^a  

^a INSTITUT DE RADIOPROTECTION ET DE SÛRETÉ NUCLÉAIRE   (France)

Author keywords

Prion; Transmissible spongiform encephalopathies

Indexed keywords

EID: 0344877098     PISSN: 12678694     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (64)

1. Laplanche JL, Chatelain J, Westaway D, Thomas S, Dussaucy M, Brugère-Picoux J, Launay JM. PrP polymorphisms associated with natural scrapie discovered by denaturing gradient gel electrophoresis. Genomics 1993 ; 15 : 30-7.
2. Brown P, Preece MA, Will RG. Friendly fire in medicine - hormones, homografts, and Creutzfeldt-Jakob disease. Lancet 1992 ; 340 : 24-7
3. Billette de Villemeur T, Beauvais P, Gourmelen M, Richardet JM. Creutzfeldt-Jakob disease in children treated with growth hormone. Lancet 1991 ; 337 : 864-5.
4. Billette de Villemeur T, Gelot A, Deslys JP, Dormont D, Duyckaens C, Jardin L, Denni J, Robin O, Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients ; a neuropathological study. Neuropathol Appl Neurobiol 1994 ; 20 : 111-7.
5. Gajdusek DC. Spongiform virus encephalopathies. J Clin Pathol (Suppl) 1972 ; 25 : 78- 83.
6. Kimberlin RH. Transmissible encephalopathies in animals. Can J Vet Res 1990 ; 54 : 30- 7.
7. Prusiner SB Biology of prion diseases. J Acq Immun Defic Syndrome 1993 ; 6 : 663-5.
8. Lee KH, Harrington MG, Premortem diagnosis of Creutzfeldt-Jakob disease by cerebrospinal fluid analysis. Lancet 1996 ; 348 : 887
9. Hisch G, Kennedy K, Gibbs CJ, Lee KH, Harrington MG. The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathies. N Engl J Med 1996 ; 335 : 924- 30.
10. Prusiner SB, Bolton DC, Groth DF, Bowman KA, Cochran SP, McKinley MP. Further purification and characterization of scrapie pnons. Biochemistry 1982 ; 21 : 6942-50.
11. Oesch B, Westaway D, Walchli M, et al. A cellular gene encodes scrapie PrP 27-30 protein. Cell 1985 ; 40 : 735- 46.
12. Bolton DC, Mckinley MR, Prusiner SB. Molecular characteristics of the major scrapie prion protein. Biochemistry 1984 ; 23 : 5898-906.
13. Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science 1982 ; 216 : 136-44.
14. Prusiner SB. Chemistry and biology of prions. Biochemistry 1992 ; 31 : 12277-88.
15. Race R. The scrapie agent in vitro. In : Transmissible spongiform encephalopathies. BW Chesebro. Springer-Verlag, 1991 : 181-93.
16. Markovits P, Dautheville C, Dormont D, Dianoux L, Latarjet R. In vitro propagation of the scrapie agent. Transformation of mouse glia and neuroblastoma cells after infection with the mouse-adapted scrapie strain c-506. Acta Neuropathologica 1983 ; 60 : 75- 80.
17. Lasmézas C, Deslys J, Dormont D. Recombinant human growth hormone and insuline-like growth factor I induce PrP gene expression in PC12 cells. Biochem Biophys Res Commun 1993 ; 196 : 1163-9.
18. Wion D, Bert ML, Brachet P. mRNAs of β-amyloïd precursor protein and PrP are regulated by nerve growth factor in PC-12 cells. Int J Dev Neurosc 1988 ; 64 : 387- 93.
19. Latarjet R. Inactivation of the agents of scrapie. Creutzfeldt-Jakob disease, and kuru by radiations. In : Slow transmissible diseases of the nervous system. Prusiner SB, Hadlow WJ, eds. Academic Press, 1979 ; 2 : 387-408.
20. Dickinson AG, Taylor DM. Resistance of scrapie to decontamination. N Engl J Med 1978 ; 299 : 1413-4.
21. Report on a WHO consultation on public health issues related to animal and human spongiform encephalopathies. Nov 12-14 (1991) ; WHO/CDS/VHP/92. 104.
22. Tateishi J, Tashima T, Kitamoto T. Practical methods for chemical inactivation of Creutzfeldt-Jakob disease pathogen. Microbiol Immunol 1991 ; 35 : 163- 6.
23. Brown P, Rohwer RG, Gajdusek DC. Newer data on the inactivation of scrapie virus or Creutzfeldt-Jakob disease virus in brain tissue. J Inf Dis 1986 ; 153 : 1145-8.
24. Prusiner SB, DeArmond SJ Prion diseases and neurodegeneration. Annu Rev Neurosci 1994 ; 17 : 311- 39
25. Prusiner SB, McKinley MP, Groth DF, Bowman KA, Mock NI, Cochran SP, Masiarz FR. Scrapie agent contains a hydrophobic protein Proc Natl Acad Sci USA 1981 ; 78 : 6675-9.
26. Merz PA, Somerville RA, Wisniewski HM, Iqbal K. Abnormal fibrils from scrapie-infected brain. Acta Neuropathologica 1981 ; 54 : 63- 74.
27. Prusiner SB. Molecular structure, biology, and genetics of prions. Adv Virus Res 1988 ; 35 : 83- 136.
28. Kretzschmar HA, Stowring LE, Westaway D, Stubblebine WH, Prusiner SB, DeArmond SJ. Molecular cloning of a human prion protein cDNA. DNA 1986 ; 5 : 315- 24
29. Laplanche JL, Beaudry P, Ripoll L, Launay JM. Protéine prion : structure, fonctions, et polymorphismes associés aux encéphalopathies spongiformes humaines Pathol Biol 1995 ; 43 : 104-13.
30. Bueler H, Fischer M, Lang Y, et al. Normal development and behaviour of mice lacking the neuronal cell surface PrP protein. Nature 1992, 356 : 577- 82.
31. Tobler I, Gaus SE, Deboer T, et al. Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature 1996 ; 380 : 639- 42.
32. Collinge J, Whittington MA, Sidle KCL, Smith CJ, Palmer MS, Clarke AR, Jefferys JGR. Prion protein is necessary for normal synaptic function Nature 1994 ; 370 : 295-7.
33. Sakagushi S, Katamine S, Nishida N, et al. Loss of cerebellar Purkinje cells in aged mice homozygous for a disupted PrP gene. Nature 1996 ; 380 : 526- 31.
34. Prusiner SB. Transgenetic Investigations of prion diseases of humans and animals. Philos Trans R Soc Lond [Biol] 1993 ; 339 : 239- 54.
35. Prusiner SB. Molecular biology and genetics of prion diseases. Philos Trans R Soc Land [Biol] 1994 ; 343 : 447- 63.
36. Hsiao KH, Groth D. Scott M, et al. Serial transmission in rodents of neurodegeneration from transgenic mice expressiong mutant prion. Proc Natl Acad Sci USA 1994 ; 91 : 9126-30.
37. Lehmann S, Harris DA. Mutant and infectious prion proteins dysplay common biochemical properties in cultured cells. J Biol Chem 1996 ; 271 : 1633-7.
38. Büeler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M, Weissmann C. Mice devoid of PrP are resistant to scrapie. Cell 1993 ; 73 : 1339-47.
39. Brandner S, Isemann S, Raeber, et al. Normal host prion protein necessary for scrapie-induced neurotoxicity. Nature 1996 ; 379 : 339- 43.
40. Kocisko DA, Come JH, Priola SA, Chesebro B, Raymond GJ, Lansbury PT, Caughey B. Cell-free formation of protease-resistant prion protein. Nature 1994 ; 370 : 471- 4.
41. Kocisko DA, Priola SA, Raymond GJ, Chesebro B, Lanshury PT, Caughey B. Species specificity in the cell-free conversion of prion protien to protease-resistant forms : a model for the scrapie species barrier. Proc Natl Acad Sci USA 1995 ; 92 : 3923-7.
42. Riek R, Hornemann S, Wider G, Billeter M, Glockshuber R, Wüthrich K. NMR structure of the mouse prion protein domain PrP (121-231). Nature 1996 ; 382 : 180- 2.
43. Dickinson AG, Outram GW. Genetic aspects of unconventional virus infections : the basis of the virino hypothesis. In : Ciba Foundation Symposium. Novel infectious agents and the central nervous system. John Wiley & Sons 1988 ; 135 : 63-83.
44. Collinge J, Palmer MS, Dryden AJ. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease. Lancet 1991 : 1441-2.
45. Deslys JP, Marcé D, Dormont D. Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob disease. J Gen Virol 1994 ; 75 : 23- 7.
46. Palmer MS, Dryden AJ, Hughes JT, Collinge J. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease. Nature 1991 ; 352 : 340- 2.
47. Will RG, Ironside JW, Zeidler M, et al. A new variant of Creutzfeldt-Jakob disease in the UK. Lancet 1996 ; 347 : 921- 5.
48. Diringer H. Sustained viremia in experimental hamster scrapie. Arch Viral 1984 ; 82 : 105- 9.
49. Lasmézas C, Cesbron JY, Deslys JP, et al. Immune system-dependent and -independent replication of the scrapie agent. J Virol 1996 ; 70 : 1292-5.
50. Prusiner SB Transgenetics and cell biology of prion diseases -investigations of PrPSc synthesis and diversity. Br Med Bull 1993 ; 49 : 873-912.
51. Forloni G, Angeretti N, Chiesa R, Monzani E, Salmona M, Bugiani O, Tagliavini F. Neurotoxicity of a prion protein fragment. Nature 1993 ; 362 : 543- 6.
52. Brown DR, Schmidt B, Kretzschmar HA. Role of microglia and host prion protein in neurotoxicity of a prion protein fragment. Nature 1996, 380 : 345- 7.
53. Manuelidis L. Essential molecular component of the CJD agent. IIIrd International symposium on subacute transmissible spongiform encephalopathies. Paris, march 18-22, 1996.
54. Dickinson AG, Outram GW. The scrapie replication-site hypothesis and its implication for pathogenesis. In : Slow transmissible diseases of the nervous system. SB Prusiner and WJ Hadlow. Academic Press, New York, 1979 ; 2 : 13-31.
55. Bolton DC, Bendheim PE. A modified host protein model of scrapie. In : Ciba Foundation Symposium. Novel infectious agents and the central nervous system. John Wiley & Sons. 1988 ; 135 : 164-77.
56. Telling GC, Scott M, Hsiao KK, et al Transmission of Creutzfeldr-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proc Natl Acad Sci USA 1994 ; 91 : 9936-40.
57. Liautard JP. Are prions misfolded molecular chaperones? FEBS Lett 1992 ; 294 : 155-7.
58. Lacroute F. Non mendelian mutation allowing ureidosuccinate acid uptake in yeast. J Bact 1971 ; 106 : 519- 22.
59. Wickner RB. [ure3] as an altered ure2 protein - Evidence for a prion analog in saccharomyces cerevisiae. Science 1994 ; 264 : 566- 9.
60. Parchi P, Castellani R, Capellari S, et al. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 1996 ; 39 : 767- 78.
61. Collinge J, Sidle KCL, Meads J, Ironside J, Hill AF. Molecular analysis of prion strain variation and the aetiology of «new variant« CJD. Nature 1996 ; 383 : 685- 90.
62. Weissmann C. A «unified theory» of prion propagation. Nature 1991 ; 352 : 679- 83.
63. Chazot G, Broussole E, Blattier T, Aguzzi A, Kopp N. New variant of Creutzfeldt-Jakob disease in a 26-year old french man. Lancet 1996 ; 347 : 1181.
64. Lasmézas CI, Desys JP, Robain O, et al. BSE transmission to macaques. Nature 1996 ; 1996 : 743-4.