MRC Prion Unit and Department of Neurodegenerative Disease, Institute of Neurology, University College London, National Hospital for Neurology and Neurosurgery, London, UK.
Neuropathol Appl Neurobiol. 2010 Dec;36(7):576-97. doi: 10.1111/j.1365-2990.2010.01129.x.
Transgenic mice expressing human prion protein in the absence of endogenous mouse prion protein faithfully replicate human prions. These models reproduce all of the key features of human disease, including long clinically silent incubation periods prior to fatal neurodegeneration with neuropathological phenotypes that mirror human prion strain diversity. Critical contributions to our understanding of human prion disease pathogenesis and aetiology have only been possible through the use of transgenic mice. These models have provided the basis for the conformational selection model of prion transmission barriers and have causally linked bovine spongiform encephalopathy with variant Creutzfeldt-Jakob disease. In the future these models will be essential for evaluating newly identified potentially zoonotic prion strains, for validating effective methods of prion decontamination and for developing effective therapeutic treatments for human prion disease.
表达人朊病毒蛋白而缺乏内源性鼠朊病毒蛋白的转基因小鼠能准确地复制人朊病毒。这些模型复制了人类疾病的所有关键特征,包括在致命神经退行性病变之前具有临床上无症状的潜伏期,其神经病理学表型与人类朊病毒株多样性相似。通过使用转基因小鼠,才有可能对人类朊病毒病的发病机制和病因学有了关键性的认识。这些模型为朊病毒传播障碍的构象选择模型提供了基础,并将牛海绵状脑病与变异克雅氏病联系起来。在未来,这些模型对于评估新发现的潜在人畜共患病朊病毒株、验证有效的朊病毒清除方法以及开发人类朊病毒病的有效治疗方法至关重要。