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. 2011 Jun;178(6):2823–2831. doi: 10.1016/j.ajpath.2011.02.046

Figure 1.

Figure 1

PrPC is up-regulated during EAE. A: PrPC expression was analyzed in WT C57Bl/6 mice in various tissue compartments throughout EAE. In all compartments analyzed (brain, spinal cord, retina, and optic nerves), PrPC expression was increased from the first day of symptoms of EAE and remained elevated until 21 days after onset of EAE, the last day of the experiment. B: PrPC levels were compared between brains from the prion-overexpressing Tg35 mouse line, the Prnp−/− knockout line, and their respective WT counterparts (WT-Tg35 mice, 129B6; and WT-Prnp, C57Bl/6). As expected, PrPC expression was greatly enhanced in the Tg35 line compared with the level in WT mice (Tg35 4.12-fold higher than WT), and was completely abolished in the Prnp−/− line. Two glycosylated forms (solid arrow) and one nonglycosylated form (open arrow) were visible. C: Quantification of PrPC expression in transgenic mice compared with their WT counterparts. D: Quantification of PrPC expression in various tissue compartments throughout EAE. *P < 0.05.