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United States Department of Agriculture

Agricultural Research Service

Title: Manganese Upregulates Cellular Prion Proteins and Inhibits the Rate of Proteinase-K Dependent Limited Proteolysis in Neuronal Cells

Authors
item Choi, Christopher - IOWA STATE UNIVERSITY
item Anantharam, Vellareddy - IOWA STATE UNIVERSITY
item Nicholson, Eric
item Richt, Juergen
item Kanthasamy, Arthi - IOWA STATE UNIVERSITY
item Kanthasamy, Anumantha - IOWA STATE UNIVERSITY

Submitted to: Society for Neuroscience Abstracts and Proceedings
Publication Type: Abstract Only
Publication Acceptance Date: August 15, 2006
Publication Date: October 14, 2006
Repository URL: http://www.sfn.org/am2006/?CFID=9935905&CFTOKEN=27189967
Citation: Choi, C.J., Anantharam, V., Nicholson, E., Richt, J., Kanthasamy, A., Kanthasamy, A.G. 2006. Manganese upregulates cellular prion proteins and inhibits the rate of proteinase-K dependent limited proteolysis in neuronal cells [abstract]. Society for Neuroscience. Paper No. 74.23.

Technical Abstract: The key event in the pathogenesis of prion diseases is the conversion of normal cellular prion proteins (PrP**c) to the proteinase K (PK) resistant, abnormal form (PrP**sc); however, the cellular mechanisms underlying the conversion remain enigmatic. Binding of divalent cations such as copper to the octapeptide repeat regions of PrP has been shown to be important for the stability of the protein. Nevertheless, the roles of other divalent cations in the normal processing of cellular PrP**c are not well understood. In the present study, we examined the effect of manganese (Mn) on PrP**c expression and degradation in neuronal cells expressing mouse prion proteins with a genetically altered novel epitope (mAb 3F4). Exposure of Mn (100µM) over the course of 24 hr increased PrP levels in both cytosolic and membrane-rich fractions in a time-dependent manner. Interestingly, Mn treatment neither increased PrP mRNA transcripts as measured by qRT-PCR nor altered the mRNA stability as determined in Actinomycin D treated cells, indicating that the effect of Mn may be at the level of post-translation and/or degradation levels of PrP. In order to determine whether the accumulation of PrP is due to impairment of the proteasomal degradation pathway by Mn, proteasomal activity and ubiquitination were measured. The results showed no significant alteration of the proteasomal degradation pathway. Notably, pulse-chase analysis showed that the PrP**c turnover rate is significantly decreased with manganese treatment. Furthermore, limited digestion with PK also revealed that manganese treatment decreased the digestion rate of the PrP. These data together clearly suggest that the divalent metal manganese can alter the normal processing of PrP, resulting in the accumulation of PrP with altered susceptibility to PK.

Last Modified: 4/24/2014
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