Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients.

Prion-Seeding Activity Is widely Distributed in Tissues of Sporadic Creutzfeldt-Jakob Disease Patients.
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DOI:
10.1016/j.ebiom.2016.08.033
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发表时间:
2016-10
期刊:
影响因子:
11.1
通讯作者:
Satoh, Katsuya
Satoh, Katsuya
中科院分区:
医学1区
文献类型:
--
作者:
Takatsuki, Hanae;Fuse, Takayuki;Nakagaki, Takehiro;Mori, Tsuyoshi;Mihara, Ban;Takao, Masaki;Iwasaki, Yasushi;Yoshida, Mari;Murayama, Shigeo;Atarashi, Ryuichiro;Nishida, Noriyuki;Satoh, Katsuya

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Human prion diseases are neurodegenerative disorders caused by abnormally folded prion proteins in the central nervous system. These proteins can be detected using the quaking-induced conversion assay. Compared with other bioassays, this assay is extremely sensitive and was used in the present study to determine prion distribution in sporadic Creutzfeldt-Jakob disease patients at autopsy. Although infectivity of the sporadic form is thought to be restricted within the central nervous system, results showed that prion-seeding activities reach 106/g from a 50% seeding dose in non-neuronal tissues, suggesting that prion-seeding activity exists in non-neural organs, and we suggested that non-neural tissues of 106/g SD50 did not exist the infectivity. Prion-seeding activities reach 106/g from a 50% seeding dose in non-neuronal tissues. Results suggest that prion-seeding activity exists in neural and non-neural organs. A major problem for the diagnosis and management of human prion diseases is the lack of rapid and high-sensitive assays to measure low prion levels. Recent studies have tried to measure prion concentrations in non-neuronal tissues, but prion levels were not sufficient. Therefore, we developed the RT-QuIC method to measure prion-seeding activity in the non-neuronal, human tissues. The SD50 levels in the spleen, kidney, lung, and liver were 5.0–6.5, with different SD50 levels in the individual cases.
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