Béranger F, Mangé A, Solassol J, Lehmann S
Institut de Génétique Humaine, CNRS UPR 1142, 141, rue de la Cardonille, 34396 Montpellier Cedex 5, France.
Biochem Biophys Res Commun. 2001 Nov 30;289(2):311-6. doi: 10.1006/bbrc.2001.5941.
In this review, we describe the generation and use of cell culture models of transmissible spongiform encephalopathies, also known as prion diseases. These models include chronically prion-infected cell lines, as well as cultures expressing variable amounts of wild-type, mutated, or chimeric prion proteins. These cell lines have been widely used to investigate the biology of both the normal and the pathological isoform of the prion protein. They have also contributed to the comprehension of the pathogenic processes occurring in transmissible spongiform encephalopathies and in the development of new therapeutic approaches of these diseases.
在本综述中,我们描述了传染性海绵状脑病(也称为朊病毒病)细胞培养模型的建立和应用。这些模型包括长期感染朊病毒的细胞系,以及表达不同数量野生型、突变型或嵌合型朊病毒蛋白的培养物。这些细胞系已被广泛用于研究朊病毒蛋白正常异构体和病理异构体的生物学特性。它们还有助于理解传染性海绵状脑病中发生的致病过程以及这些疾病新治疗方法的开发。