Peripheral circulation of the prion infectious agent in transgenic mice expressing the ovine prion protein gene in neurons only.

BACKGROUND For prion diseases, even if a large body of evidence indicates that both the lymphoreticular system (LRS) and peripheral nerves are involved in scrapie neuroinvasion, the processes by which prions invade the central nervous system are only partially understood. METHODS Transgenic Tg(OvPrP4) mice, which express the ovine prion protein (PrP) gene under the rat neuron-specific enolase promoter on a knockout background, were used to study prion extracerebral circulation after scrapie prions were inoculated via the intracerebral (ic) and the intraperitoneal (ip) route. RESULTS Surprisingly, PrP(Sc) was detected in the spleens of mice inoculated ic with prions. Moreover, the absence of the ovine PrP(C) in nonneural tissue at the periphery did not stop neuroinvasion after ip challenge. Additionally, pilot studies performed in Tg(OvPrP4) mice that had undergone splenectomy before ic prion inoculation showed that the time course of the disease is delayed. CONCLUSIONS Given that these mice express the ovine PrP gene in neuronal cells but not in nonnervous tissue, our results suggest that PrP(C) expressed by cells of the LRS are not necessary for neuroinvasion or for their ability to accumulate PrP(Sc) and emphasize the importance of extracerebral circulation of PrP(C) or PrP(Sc) for the development of the disease.