Spontaneous prion disease in homozygous and heterozygous transgenic mouse models of T188K genetic Creutzfeldt-Jakob disease

• Published in: Neurobiology of aging 2023-11, Vol.131, p.156-169
• Main Authors: Wu, Yue-Zhang, Gao, Li-Ping, Chen, Dong-Dong, Liang, Dong-Lin, Chen, Jia, Xiao, Kang, Hu, Chao, Chen, Cao, Shi, Qi, Dong, Xiao-Ping
• Format: Article
• Language: English
• Subjects: Creutzfeldt-Jakob disease; Genetic; Prion; T188K mutation; Transgenic mouse
• ISSN: 0197-4580; 1558-1497
• DOI: 10.1016/j.neurobiolaging.2023.07.024

Genetic Creutzfeldt-Jakob disease with T188K mutation (T188K gCJD) is the most frequent genetic prion disease in China. To explore the penetration of T188K mutation and the pathogenesis of T188K gCJD, we constructed 2 lines of transgenic mouse models: homozygous Tg188K+/+ mice containing T188K mutation in 2 alleles of human PRNP background and heterozygous Tg188K+/- mice containing 1 allele of T188K human PRNP and 1 allele of the wild-type mouse PRNP. Spontaneous neurological illnesses were identified in all Tg188K mice at their old ages (750–800 days old). About half of the Tg188K mice died prior to the final observation (930 days old). Extensive spongiosis, PrPSc deposit, and reactive gliosis of astrocytes and microglia are neuropathologically identified, showing time-dependent exacerbation. Proteinase K-resistant PrP was detected in the brain, muscle, and intestine tissues, and positive real-time quaking-induced conversion reactions were elicited by the brain and muscle tissues of Tg188K mice. Those data verify that the constructed Tg188K mice highly mimic the clinicopathology of human T188K gCJD, strongly indicating the pathogenicity of T188K mutated PrP.