J Gen Virol Tips for Better Browsing
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 85 (2004), 1785-1790; DOI 10.1099/vir.0.19754-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ishikawa, K.
Right arrow Articles by Iwaki, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ishikawa, K.
Right arrow Articles by Iwaki, T.
Agricola
Right arrow Articles by Ishikawa, K.
Right arrow Articles by Iwaki, T.
© 2004 Society for General Microbiology

Amyloid imaging probes are useful for detection of prion plaques and treatment of transmissible spongiform encephalopathies

Kensuke Ishikawa1, Katsumi Doh-ura1,{dagger}, Yukitsuka Kudo2, Noriyuki Nishida3, Ikuko Murakami-Kubo1, Yukio Ando4, Tohru Sawada2 and Toru Iwaki1

1 Department of Neuropathology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan
2 BF Research Institute Inc., Osaka 565-0873, Japan
3 Department of Bacteriology, Nagasaki University School of Medicine, Nagasaki, 852-8501, Japan
4 Department of Laboratory Medicine, Kumamoto University, Kumamoto 860-0081, Japan

Correspondence
Kensuke Ishikawa
kensuke{at}np.med.kyushu-u.ac.jp
Katsumi Doh-ura
doh-ura{at}mail.tains.tohoku.ac.jp

Diagnostic imaging probes have been developed to monitor cerebral amyloid lesions in patients with neurodegenerative disorders. A thioflavin derivative, 2-[4'-(methylamino)phenyl] benzothiazole (BTA-1) and a Congo red derivative, (trans, trans),-1-bromo-2,5-bis-(3-hydroxycarbonyl-4-hydroxy)styrylbenzene (BSB) are representative chemicals of these probes. In this report, the two chemicals were studied in transmissible spongiform encephalopathies (TSE). Both BTA-1 and BSB selectively bound to compact plaques of prion protein (PrP), not only in the brain specimens of certain types of human TSE, but also in the brains of TSE-infected mice when the probes were injected intravenously. The chemicals bound to plaques in the brains were stable and could be detected for more than 42 h post-injection. In addition, the chemicals inhibited abnormal PrP formation in a cellular model of TSE with IC50 values of 4 nM for BTA-1 and 1·4 µM for BSB. In an experimental mouse model, the intravenous injection of 1 mg BSB prolonged the incubation period by 14 %. This efficacy was only observed against the RML strain and not the other strains examined. These observations suggest that these chemicals bind directly to PrP aggregates and inhibit new formation of abnormal PrP in a strain-dependent manner. Both BTA-1 and BSB can be expected to be lead chemicals not only for imaging probes but also for therapeutic drugs for TSEs caused by certain strains.

{dagger}Present address: Department of Prion Research, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.




This article has been cited by other articles:


Home page
J. Virol.Home page
P. B. McIntosh, S. R. Martin, D. J. Jackson, J. Khan, E. R. Isaacson, L. Calder, K. Raj, H. M. Griffin, Q. Wang, P. Laskey, et al.
Structural Analysis Reveals an Amyloid Form of the Human Papillomavirus Type 16 E1{wedge}E4 Protein and Provides a Molecular Basis for Its Accumulation
J. Virol., August 15, 2008; 82(16): 8196 - 8203.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
Y. Kawasaki, K. Kawagoe, C.-j. Chen, K. Teruya, Y. Sakasegawa, and K. Doh-ura
Orally Administered Amyloidophilic Compound Is Effective in Prolonging the Incubation Periods of Animals Cerebrally Infected with Prion Diseases in a Prion Strain-Dependent Manner
J. Virol., December 1, 2007; 81(23): 12889 - 12898.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
I. P. Lipscomb, R. Herve, K. Harris, H. Pinchin, R. Collin, and C. W. Keevil
Amyloid-specific fluorophores for the rapid, sensitive in situ detection of prion contamination on surgical instruments
J. Gen. Virol., September 1, 2007; 88(9): 2619 - 2626.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
G. J. Raymond, E. A. Olsen, K. S. Lee, L. D. Raymond, P. K. Bryant III, G. S. Baron, W. S. Caughey, D. A. Kocisko, L. E. McHolland, C. Favara, et al.
Inhibition of Protease-Resistant Prion Protein Formation in a Transformed Deer Cell Line Infected with Chronic Wasting Disease
J. Virol., January 15, 2006; 80(2): 596 - 604.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 by the Society for General Microbiology.