Involvement of PrPC in kainate-induced excitotoxicity in several mouse strains
The cellular prion protein (PrP C) has been associated with a plethora of cellular functions ranging from cell cycle to neuroprotection. Mice lacking PrP C show an increased susceptibility to epileptic seizures; the protein, then, is neuroprotective. However, lack of experimental reproducibility has led to considering the possibility that other factors besides PrP C deletion, such as the genetic background of mice or the presence of so-called â Prnp flanking genesâ € might contribute to the reported susceptibility. Here, we performed a comparative analysis of seizure-susceptibility using characterized Prnp +/+ and Prnp 0/0 mice of B6129, B6.129, 129/Ola or FVB/N genetic backgrounds. Our study indicates that PrP C plays a role in neuroprotection in KA-treated cells and mice. For this function, PrP C should contain the aa32-93 region and needs to be linked to the membrane. In addition, some unidentified â Prnp-flanking genesâ €play a role parallel to PrP C in the KA-mediated responses in B6129 and B6.129 Prnp 0/0 mice.
Main Authors: | , , , , , , , , , |
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Format: | journal article biblioteca |
Language: | eng |
Published: |
2015
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Online Access: | http://hdl.handle.net/20.500.12792/4969 |
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