Literature DB >> 18590830

Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture.

Victoria A Lawson1, Laura J Vella, James D Stewart, Robyn A Sharples, Helen Klemm, Dorothy M Machalek, Colin L Masters, Roberto Cappai, Steven J Collins, Andrew F Hill.   

Abstract

Cell based models used for the study of prion diseases have traditionally employed mouse-adapted strains of sheep scrapie prions. To date, attempts to generate human prion propagation in cell culture have been unsuccessful. Rabbit kidney epithelial cells (RK13) are permissive to infection with prions from a variety of species upon expression of cognate PrP transgenes. We explored RK13 cells expressing human PrP for their utility as a cell line capable of sustaining infection with human prions. RK13 cells processed exogenously expressed human PrP similarly to exogenously expressed mouse PrP but were not permissive to infection when exposed to sporadic Creutzfeldt-Jakob disease prions. Transmission of the same sporadic Creutzfeldt Jakob disease prions to wild-type mice generated a strain of mouse-adapted human prions, which efficiently propagated in RK13 cells expressing mouse PrP, demonstrating these cells are permissive to infection by mouse-adapted human prions. Our observations underscore the likelihood that, in contrast to prions derived from non-human mammals, additional unidentified cofactors or subcellular environment are critical for the generation of human prions.

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Year:  2008        PMID: 18590830     DOI: 10.1016/j.biocel.2008.05.024

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  32 in total

1.  Near-infrared fluorescence imaging of apoptotic neuronal cell death in a live animal model of prion disease.

Authors:  Victoria A Lawson; Cathryn L Haigh; Blaine Roberts; Vijaya B Kenche; Helen M J Klemm; Colin L Masters; Steven J Collins; Kevin J Barnham; Simon C Drew
Journal:  ACS Chem Neurosci       Date:  2010-09-30       Impact factor: 4.418

2.  The yeast Sup35NM domain propagates as a prion in mammalian cells.

Authors:  Carmen Krammer; Dmitry Kryndushkin; Michael H Suhre; Elisabeth Kremmer; Andreas Hofmann; Alexander Pfeifer; Thomas Scheibel; Reed B Wickner; Hermann M Schätzl; Ina Vorberg
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-29       Impact factor: 11.205

3.  The prion protein preference of sporadic Creutzfeldt-Jakob disease subtypes.

Authors:  Helen M J Klemm; Jeremy M Welton; Colin L Masters; Genevieve M Klug; Alison Boyd; Andrew F Hill; Steven J Collins; Victoria A Lawson
Journal:  J Biol Chem       Date:  2012-08-28       Impact factor: 5.157

4.  A transfectant RK13 cell line permissive to classical caprine scrapie prion propagation.

Authors:  Rohana P Dassanayake; Dongyue Zhuang; Thomas C Truscott; Sally A Madsen-Bouterse; Katherine I O'Rourke; David A Schneider
Journal:  Prion       Date:  2016-03-03       Impact factor: 3.931

5.  Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.

Authors:  Bradley M Coleman; Christopher F Harrison; Belinda Guo; Colin L Masters; Kevin J Barnham; Victoria A Lawson; Andrew F Hill
Journal:  J Virol       Date:  2013-12-18       Impact factor: 5.103

6.  Conservation of a glycine-rich region in the prion protein is required for uptake of prion infectivity.

Authors:  Christopher F Harrison; Victoria A Lawson; Bradley M Coleman; Yong-Sun Kim; Colin L Masters; Roberto Cappai; Kevin J Barnham; Andrew F Hill
Journal:  J Biol Chem       Date:  2010-03-31       Impact factor: 5.157

7.  Residues surrounding the glycosylphosphatidylinositol anchor attachment site of PrP modulate prion infection: insight from the resistance of rabbits to prion disease.

Authors:  Rebecca M Nisbet; Christopher F Harrison; Victoria A Lawson; Colin L Masters; Roberto Cappai; Andrew F Hill
Journal:  J Virol       Date:  2010-04-28       Impact factor: 5.103

8.  Prion disease is accelerated in mice lacking stress-induced heat shock protein 70 (HSP70).

Authors:  Charles E Mays; Enrique Armijo; Rodrigo Morales; Carlos Kramm; Andrea Flores; Anjana Tiwari; Jifeng Bian; Glenn C Telling; Tej K Pandita; Clayton R Hunt; Claudio Soto
Journal:  J Biol Chem       Date:  2019-07-18       Impact factor: 5.157

9.  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

10.  Glycosaminoglycan sulphation affects the seeded misfolding of a mutant prion protein.

Authors:  Victoria A Lawson; Brooke Lumicisi; Jeremy Welton; Dorothy Machalek; Katrina Gouramanis; Helen M Klemm; James D Stewart; Colin L Masters; David E Hoke; Steven J Collins; Andrew F Hill
Journal:  PLoS One       Date:  2010-08-23       Impact factor: 3.240

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