Literature DB >> 24860095

Mouse models for studying the formation and propagation of prions.

Joel C Watts1, Stanley B Prusiner2.   

Abstract

Prions are self-propagating protein conformers that cause a variety of neurodegenerative disorders in humans and animals. Mouse models have played key roles in deciphering the biology of prions and in assessing candidate therapeutics. The development of transgenic mice that form prions spontaneously in the brain has advanced our understanding of sporadic and genetic prion diseases. Furthermore, the realization that many proteins can become prions has necessitated the development of mouse models for assessing the potential transmissibility of common neurodegenerative diseases. As the universe of prion diseases continues to expand, mouse models will remain crucial for interrogating these devastating illnesses.
© 2014 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  Animal Model; Neurodegenerative Disease; Pathology; Prion; Protein Aggregation

Mesh:

Substances:

Year:  2014        PMID: 24860095      PMCID: PMC4106304          DOI: 10.1074/jbc.R114.550707

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  99 in total

1.  Predicting susceptibility and incubation time of human-to-human transmission of vCJD.

Authors:  M T Bishop; P Hart; L Aitchison; H N Baybutt; C Plinston; V Thomson; N L Tuzi; M W Head; J W Ironside; R G Will; J C Manson
Journal:  Lancet Neurol       Date:  2006-05       Impact factor: 44.182

2.  Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice.

Authors:  Karah E Nazor; Franziska Kuhn; Tanya Seward; Mike Green; Daniel Zwald; Mario Pürro; Jaqueline Schmid; Karin Biffiger; Aisling M Power; Bruno Oesch; Alex J Raeber; Glenn C Telling
Journal:  EMBO J       Date:  2005-06-16       Impact factor: 11.598

Review 3.  A general model of prion strains and their pathogenicity.

Authors:  John Collinge; Anthony R Clarke
Journal:  Science       Date:  2007-11-09       Impact factor: 47.728

4.  Orally administered amyloidophilic compound is effective in prolonging the incubation periods of animals cerebrally infected with prion diseases in a prion strain-dependent manner.

Authors:  Yuri Kawasaki; Keiichi Kawagoe; Chun-jen Chen; Kenta Teruya; Yuji Sakasegawa; Katsumi Doh-ura
Journal:  J Virol       Date:  2007-09-19       Impact factor: 5.103

5.  Prion clearance in bigenic mice.

Authors:  Jiri G Safar; Stephen J DeArmond; Katarzyna Kociuba; Camille Deering; Svetlana Didorenko; Essia Bouzamondo-Bernstein; Stanley B Prusiner; Patrick Tremblay
Journal:  J Gen Virol       Date:  2005-10       Impact factor: 3.891

6.  Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models.

Authors:  Qingzhong Kong; Shenghai Huang; Wenquan Zou; Difernando Vanegas; Meiling Wang; Di Wu; Jue Yuan; Mengjie Zheng; Hua Bai; Huayun Deng; Ken Chen; Allen L Jenny; Katherine O'Rourke; Ermias D Belay; Lawrence B Schonberger; Robert B Petersen; Man-Sun Sy; Shu G Chen; Pierluigi Gambetti
Journal:  J Neurosci       Date:  2005-08-31       Impact factor: 6.167

7.  Resistance to chronic wasting disease in transgenic mice expressing a naturally occurring allelic variant of deer prion protein.

Authors:  Kimberly Meade-White; Brent Race; Matthew Trifilo; Alex Bossers; Cynthia Favara; Rachel Lacasse; Michael Miller; Elizabeth Williams; Michael Oldstone; Richard Race; Bruce Chesebro
Journal:  J Virol       Date:  2007-02-21       Impact factor: 5.103

8.  Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice.

Authors:  Giovanna R Mallucci; Melanie D White; Michael Farmer; Andrew Dickinson; Husna Khatun; Andrew D Powell; Sebastian Brandner; John G R Jefferys; John Collinge
Journal:  Neuron       Date:  2007-02-01       Impact factor: 17.173

9.  Efficient transmission and characterization of Creutzfeldt-Jakob disease strains in bank voles.

Authors:  Romolo Nonno; Michele A Di Bari; Franco Cardone; Gabriele Vaccari; Paola Fazzi; Giacomo Dell'Omo; Claudia Cartoni; Loredana Ingrosso; Aileen Boyle; Roberta Galeno; Marco Sbriccoli; Hans-Peter Lipp; Moira Bruce; Maurizio Pocchiari; Umberto Agrimi
Journal:  PLoS Pathog       Date:  2006-02-24       Impact factor: 6.823

10.  Prominent and persistent extraneural infection in human PrP transgenic mice infected with variant CJD.

Authors:  Vincent Béringue; Annick Le Dur; Philippe Tixador; Fabienne Reine; Laurence Lepourry; Armand Perret-Liaudet; Stéphane Haïk; Jean-Luc Vilotte; Michel Fontés; Hubert Laude
Journal:  PLoS One       Date:  2008-01-09       Impact factor: 3.240

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  46 in total

1.  Towards authentic transgenic mouse models of heritable PrP prion diseases.

Authors:  Joel C Watts; Kurt Giles; Matthew E C Bourkas; Smita Patel; Abby Oehler; Marta Gavidia; Sumita Bhardwaj; Joanne Lee; Stanley B Prusiner
Journal:  Acta Neuropathol       Date:  2016-06-28       Impact factor: 17.088

Review 2.  Neurodegenerative Disease Transmission and Transgenesis in Mice.

Authors:  Brittany N Dugger; Daniel P Perl; George A Carlson
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-11-01       Impact factor: 10.005

Review 3.  Bioassays and Inactivation of Prions.

Authors:  Kurt Giles; Amanda L Woerman; David B Berry; Stanley B Prusiner
Journal:  Cold Spring Harb Perspect Biol       Date:  2017-08-01       Impact factor: 10.005

4.  Alterations in neuronal metabolism contribute to the pathogenesis of prion disease.

Authors:  Julie-Myrtille Bourgognon; Jereme G Spiers; Hannah Scheiblich; Alexey Antonov; Sophie J Bradley; Andrew B Tobin; Joern R Steinert
Journal:  Cell Death Differ       Date:  2018-06-18       Impact factor: 15.828

Review 5.  Analysis of RNA from Alzheimer's Disease Post-mortem Brain Tissues.

Authors:  Christian Clement; James M Hill; Prerna Dua; Frank Culicchia; Walter J Lukiw
Journal:  Mol Neurobiol       Date:  2015-01-29       Impact factor: 5.590

6.  Region-specific glial homeostatic signature in prion diseases is replaced by a uniform neuroinflammation signature, common for brain regions and prion strains with different cell tropism.

Authors:  Natallia Makarava; Jennifer Chen-Yu Chang; Kara Molesworth; Ilia V Baskakov
Journal:  Neurobiol Dis       Date:  2020-01-27       Impact factor: 5.996

Review 7.  Prions and prion-like proteins.

Authors:  Paul E Fraser
Journal:  J Biol Chem       Date:  2014-05-23       Impact factor: 5.157

8.  Engineering a murine cell line for the stable propagation of hamster prions.

Authors:  Matthew E C Bourkas; Hamza Arshad; Zaid A M Al-Azzawi; Ondrej Halgas; Ronald A Shikiya; Mohadeseh Mehrabian; Gerold Schmitt-Ulms; Jason C Bartz; Joel C Watts
Journal:  J Biol Chem       Date:  2019-01-31       Impact factor: 5.157

9.  Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.

Authors:  Joel C Watts; Kurt Giles; Daniel J Saltzberg; Brittany N Dugger; Smita Patel; Abby Oehler; Sumita Bhardwaj; Andrej Sali; Stanley B Prusiner
Journal:  J Virol       Date:  2016-10-14       Impact factor: 5.103

10.  Two superoxide dismutase prion strains transmit amyotrophic lateral sclerosis-like disease.

Authors:  Elaheh Ekhtiari Bidhendi; Johan Bergh; Per Zetterström; Peter M Andersen; Stefan L Marklund; Thomas Brännström
Journal:  J Clin Invest       Date:  2016-05-03       Impact factor: 14.808

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