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2 Uppsatser om Prion - Sida 1 av 1
Prion infection of ovine cell culture with a natural Swedish scrapie isolate from 1986
Scrapie is an infectious neurologic disease in sheep caused by Prions, corresponding to transmissible spongiform encephalopathies (TSEs) in other species. The Prion is presumably constituted of PrPSc, the misfolded form of the normal endogenous Prion protein, PrPC, which is found in practically all cells in the body. PrPSc can induce a conformational change in PrPC and misfold it as an imprint of itself; this is how Prions amplify and spread. The process of conformational change is poorly understood and there might exist intermediate forms between PrPC and PrPSc. Bioassay using mice has traditionally been the golden standard in Prion studies but is limited by cost and time.
Exosomes as a potential mechanism of intercellular spread of prion protein
Structural rationalizations and regionalization of the agricultural sector in Sweden has lead to unevenness in thedistribution of plant nutrients. Nutrients are lost from crop producing farms as harvest products are sold, whilefarms with animal production often have manure in excess of their needs. In addition to this the retention ofwater and nutrients in naturally occurring wetlands has decreased due to a reduction of wetlands in number andsize in the agricultural landscape. This increases nutrient levels in agricultural run-off and causes eutrophicationas well as nutrient losses from arable soils. One potential solution to both problems would be to store nutrientrichsurface water from agricultural areas and use it for irrigation of agricultural crops.