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Resistance of cell lines to prion toxicity aided by phospho-ERK expression


Reference:

Uppington, K. M. and Brown, D. R., 2008. Resistance of cell lines to prion toxicity aided by phospho-ERK expression. Journal of Neurochemistry, 105 (3), pp. 842-852.

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Official URL:

http://dx.doi.org/10.1111/j.1471-4159.2007.05192.x

Abstract

Prion diseases are fatal neurodegenerative disorders. They are characterised by neuronal loss and the accumulation of an abnormal protein in the CNS. Cell lines exist that express the toxic form of the prion protein (PrP) with little evidence of cell death. Other cell based models studying the mechanism by which cell death occurs employ exogenous application of peptides or fragments of PrP. In this study, we demonstrated that full-length recombinant PrP binding manganese was toxic to PrP-expressing cell lines and primary neuronal cultures but not to PrP-knockout neurones. This toxic form of PrP was also toxic to cell lines equivalently regardless of whether they were infected with scrapie or not. Both scrapie-infected cells and cells resistant to the toxicity of PrP showed increased levels of phosphorylated ERK protein. Scrapie-infected cells also showed elevated levels of caspase 12. Inhibition of phospho-ERK resulted in increased cell death suggesting the increased levels of phospho-ERK served a protective effect. These results suggest that scrapie-infected cell lines resist the toxicity of the prions they generate because they produce only low levels of abnormal protein and have increased resistance to apoptotic signs because of heightened activity of the MAP kinase pathway.

Details

Item Type Articles
CreatorsUppington, K. M.and Brown, D. R.
DOI10.1111/j.1471-4159.2007.05192.x
DepartmentsFaculty of Science > Biology & Biochemistry
RefereedYes
StatusPublished
ID Code3409
Additional InformationID number: ISI:000255139200024

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