Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients

Acta Neuropathologica

Volumn 116, Issue 5, 2008, Pages 561-566

  Kobayashi, Atsushi ^a   Arima, Kunimasa ^b   Ogawa, Masafumi ^b   Murata, Miho ^b   Fukuda, Takahiro ^c   Kitamoto, Tetsuyuki ^a  

^a TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b National Center of Neurology and Psychiatry   (Japan)

^c JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Amyloid plaque; Creutzfeldt Jakob disease; Prion protein; White matter

Indexed keywords

AMYLOID PRECURSOR PROTEIN; PRION PROTEIN;

ADULT; AGED; AKINETIC MUTISM; AMNESIA; ARTICLE; CASE REPORT; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DISEASE CLASSIFICATION; DISEASE DURATION; DISORIENTATION; ELECTROENCEPHALOGRAM; FATIGUE; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MYOCLONUS; NEUROPATHOLOGY; PRIORITY JOURNAL; SENILE PLAQUE; WHITE MATTER;

AGED; BLOTTING, WESTERN; BRAIN; CREUTZFELDT-JAKOB SYNDROME; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MALE; MIDDLE AGED; NEURONS; PRIONS; SENILE PLAQUES;

EID: 54149085116     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-008-0425-8     Document Type: Article

References (21)

1. Asano M, Mohri S, Ironside JW, Ito M, Tamaoki N, Kitamoto T (2006) vCJD prion acquires altered virulence through trans-species infection. Biochem Biophys Res Commun 342:293-299. doi: 10.1016/j.bbrc.2006.01.149
2. Cali I, Castellani R, Yuan J et al (2006) Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain 129:2266-2277. doi: 10.1093/ brain/awl224
3. Grathwohl KUD, Horiuchi M, Ishiguro N, Shinagawa M (1996) Improvement of PrP Sc -detection in mouse spleen early at the preclinical stage of scrapie with collagenase-completed tissue homogenization and Sarkosyl-NaCl extraction of PrP Sc. Arch Virol 141:1863-1874. doi: 10.1007/BF01718200
4. Ishida C, Kakishima A, Okino S et al (2003) Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques. Neurology 60:514-517
5. Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G (2006) Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type. Acta Neuropathol 112:561-571. doi: 10.1007/ s00401-006-0111-7
6. Kitamoto T, Shin RW, Doh-ura K et al (1992) Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 140:1285-1294
7. Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J (1993) Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. Biochem Biophys Res Commun 191:709-714. doi: 10.1006/bbrc.1993.1275
8. Kobayashi A, Asano M, Mohri S, Kitamoto T (2007) Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain. J Biol Chem 282:30022-30028. doi: 10.1074/jbc.M704597200
9. Koo EH, Sisodia SS, Archer DR et al (1990) Precursor of amyloid protein in Alzheimer disease undergoes fast anterograde axonal transport. Proc Natl Acad Sci USA 87:1561-1565. doi: 10.1073/pnas.87.4.1561
10. Muramoto T, Tanaka T, Kitamoto N et al (2000) Analyasis of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu. Neurosci Lett 288:179-182. doi: 10.1016/S0304-3940(00)01232-5
11. Murayama H, Shin RW, Higuchi J, Shibuya S, Muramoto T, Kitamoto T (1999) Interaction of aluminum with PHFτ in Alzheimer;s disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method. Am J Pathol 155:877-885
12. Ohgami T, Kitamoto T, Shin RW, Kaneko Y, Ogomori K, Tateishi J (1991) Increased senile plaques without microglia in Alzheimer's disease. Acta Neuropathol 81:242-247. doi: 10.1007/BF00305864
13. Ohgami T, Kitamoto T, Tateishi J (1992) Alzheimer's amyloid precursor protein accumulates within axonal swellings in human brain lesions. Neurosci Lett 136:75-78. doi: 10.1016/0304-3940(92)90651-M
14. Parchi P, Castellani R, Capellari S et al (1996) Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Ann Neurol 39:767-778. doi: 10.1002/ana.410390613
15. Parchi P, Capellari S, Chen SG et al (1997) Typing prion isoforms. Nature 386:232-233. doi: 10.1038/386232a0
16. Parchi P, Giese A, Capellari S et al (1999) Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 46:224-233. doi: 10.1002/ 1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
17. Parchi P, Zou W, Wang W et al (2000) Genetic influence on the structural variations of the abnormal prion protein. Proc Natl Acad Sci USA 97:10168-10172. doi: 10.1073/pnas.97.18.10168
18. Pocchiari M, Puopolo M, Croes EA et al (2004) Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain 127:2348-2359. doi: 10.1093/brain/ awh249
19. Satoh K, Muramoto T, Tanaka T et al (2003) Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases. J Gen Virol 84:2885-2893. doi: 10.1099/vir.0.19236-0
20. Shin RW, Iwaki T, Kitamoto T, Tateishi J (1991) Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues. Lab Invest 64:693-702
21. Tomita S, Ozaki T, Taru H et al (1999) Interaction of a neuron-specific protein containing PDZ domains with Alzheimer's amyloid precursor protein. J Biol Chem 274:2243-2254. doi: 10.1074/jbc.274.4.2243