Literature DB >> 2468821

Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques.

T Kitamoto1, J Tateishi, H Sawa, K Doh-Ura.   

Abstract

Kuru plaque is a pathognomonic feature in the brain of patients with Creutzfeldt-Jakob disease (CJD) and in the brain of CJD-infected mice. Kuru plaques from CJD-infected mice were immunolabeled with rabbit anti-murine prion protein (PrP) absorbed with human PrP, but not so with mouse anti-human PrP. Therefore, the murine kuru plaque is composed of the host (mouse) PrP and can be distinguished antigenically from human PrP. Immunostaining using the anti-murine PrP and formic acid enhancement on tissue sections revealed not only birefringent kuru plaques but also nonbirefringent diffuse and small PrP accumulations. This immunohistochemical detection of kuru plaques provides more positive evidence than heretofore employed histochemical approaches. There were kuru plaques in brains of the first passage mice inoculated with tissues from 30 (91%) of 33 patients with CJD, the 3 negative patients belonging to a type of Gerstmann-Sträussler syndrome. Tissues from 6 other demented patients did not produce kuru plaques. In the evaluation of spongiform changes, mice inoculated with tissues from 23 (70%) of 33 patients were considered cases of successful transmission. In some mice, kuru plaques were present in the absence of spongiform changes. Further inoculations from 9 mice with kuru plaques but no spongiform changes were successful in almost all mice. Therefore, mice with murine kuru plaques in the absence of spongiform changes are also infectious. Thus, the presence of murine-specific kuru plaques can serve as another hallmark of a successful transmission.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2468821

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  10 in total

1.  Human and experimental spongiform encephalopathies: recent progress in pathogenesis.

Authors:  M C Dal Canto
Journal:  Ital J Neurol Sci       Date:  1991-04

2.  Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study.

Authors:  T Muramoto; T Kitamoto; J Tateishi; I Goto
Journal:  Am J Pathol       Date:  1993-11       Impact factor: 4.307

3.  Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments.

Authors:  J Tateishi; T Kitamoto; K Doh-ura; J W Boellaard; J Peiffer
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

4.  Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease.

Authors:  T Muramoto; T Kitamoto; M Z Hoque; J Tateishi; I Goto
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

5.  The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.

Authors:  T Muramoto; T Kitamoto; J Tateishi; I Goto
Journal:  Am J Pathol       Date:  1992-06       Impact factor: 4.307

6.  Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.

Authors:  G C Telling; M Scott; K K Hsiao; D Foster; S L Yang; M Torchia; K C Sidle; J Collinge; S J DeArmond; S B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  1994-10-11       Impact factor: 11.205

7.  Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome.

Authors:  M Miyazono; T Kitamoto; T Iwaki; J Tateishi
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

8.  Spontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.

Authors:  Joel C Watts; Kurt Giles; Jan Stöhr; Abby Oehler; Sumita Bhardwaj; Sunny K Grillo; Smita Patel; Stephen J DeArmond; Stanley B Prusiner
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-13       Impact factor: 11.205

Review 9.  Prion disease: experimental models and reality.

Authors:  Sebastian Brandner; Zane Jaunmuktane
Journal:  Acta Neuropathol       Date:  2017-01-13       Impact factor: 17.088

Review 10.  Invited Review: The role of prion-like mechanisms in neurodegenerative diseases.

Authors:  Z Jaunmuktane; S Brandner
Journal:  Neuropathol Appl Neurobiol       Date:  2020-02-11       Impact factor: 8.090

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.