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本文引用的文献

1
Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C).不同人类朊病毒中的 PrPSc 小蛋白酶敏感寡聚物决定 PrP(C)的转化速率。
PLoS Pathog. 2012;8(8):e1002835. doi: 10.1371/journal.ppat.1002835. Epub 2012 Aug 2.
2
Initial fate of prions upon peripheral infection: half-life, distribution, clearance, and tissue uptake.外周感染时朊病毒的初始命运:半衰期、分布、清除和组织摄取。
FASEB J. 2011 Aug;25(8):2792-803. doi: 10.1096/fj.11-180729. Epub 2011 May 9.
3
Generation of a new form of human PrP(Sc) in vitro by interspecies transmission from cervid prions.通过种间传播从鹿朊病毒生成新型人类 PrP(Sc)。
J Biol Chem. 2011 Mar 4;286(9):7490-5. doi: 10.1074/jbc.M110.198465. Epub 2011 Jan 5.
4
Estimating prion concentration in fluids and tissues by quantitative PMCA.通过定量 PMCA 估计液体和组织中的朊病毒浓度。
Nat Methods. 2010 Jul;7(7):519-20. doi: 10.1038/nmeth.1465. Epub 2010 May 30.
5
Generating a prion with bacterially expressed recombinant prion protein.用细菌表达的重组朊病毒蛋白生成朊病毒。
Science. 2010 Feb 26;327(5969):1132-5. doi: 10.1126/science.1183748. Epub 2010 Jan 28.
6
Transport of prion protein across the blood-brain barrier.朊病毒蛋白通过血脑屏障的转运。
Exp Neurol. 2009 Jul;218(1):162-7. doi: 10.1016/j.expneurol.2009.04.025. Epub 2009 May 5.
7
Characteristics of 263K scrapie agent in multiple hamster species.263K 羊瘙痒病病原体在多种仓鼠物种中的特性
Emerg Infect Dis. 2009 Feb;15(2):207-15. doi: 10.3201/eid1502.081173.
8
PrP(Sc) of scrapie 263K propagates efficiently in spleen and muscle tissues with protein misfolding cyclic amplification.羊瘙痒病263K毒株的朊病毒蛋白(Sc型)通过蛋白质错误折叠循环扩增在脾脏和肌肉组织中高效增殖。
Virus Res. 2009 Apr;141(1):26-33. doi: 10.1016/j.virusres.2008.12.010. Epub 2009 Jan 20.
9
Reduction of prion infectivity in packed red blood cells.降低浓缩红细胞中的朊病毒传染性。
Biochem Biophys Res Commun. 2008 Dec 12;377(2):373-378. doi: 10.1016/j.bbrc.2008.09.141. Epub 2008 Oct 11.
10
Detection of infectious prions in urine.尿液中传染性朊病毒的检测。
FEBS Lett. 2008 Sep 22;582(21-22):3161-6. doi: 10.1016/j.febslet.2008.08.003. Epub 2008 Aug 13.

实验性仓鼠中,外周给药的朊病毒以亚感染量到达大脑。

Peripherally administrated prions reach the brain at sub-infectious quantities in experimental hamsters.

机构信息

Protein Misfolding Disorders Laboratory, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Medical School at Houston, Houston, TX 77030, USA; Department of Laboratory Animal Science, School of Basic Medical Science, Capital Medical University, Beijing 100069, China.

Protein Misfolding Disorders Laboratory, Mitchell Center for Alzheimer's Disease and Related Brain Disorders, University of Texas Medical School at Houston, Houston, TX 77030, USA.

出版信息

FEBS Lett. 2014 Mar 3;588(5):795-800. doi: 10.1016/j.febslet.2014.01.038. Epub 2014 Feb 1.

DOI:10.1016/j.febslet.2014.01.038
PMID:24492001
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3980850/
Abstract

The mechanisms implicated in prion infection and tissue distribution are not completely understood. In this study we investigated the levels of 263K prions in brain and spleen of Syrian hamsters few days after intra-peritoneal challenge. For this purpose we utilized the PMCA technology which permits to detect as little as few PrP(Sc) molecules. Our results show that peripherally administered prions directly reach the brain, although at levels below the minimum necessary to produce disease. PrP(Sc) remains in the brain several days after administration suggesting inefficient clearance or early replication. Understanding the fate of the infectious agent after administration and its uptake in different organs and fluids may provide useful information to develop strategies to minimize further spreading of prion diseases.

摘要

朊病毒感染和组织分布的机制尚不完全清楚。在这项研究中,我们研究了腹腔内 challenged 几天后叙利亚仓鼠大脑和脾脏中 263K 朊病毒的水平。为此,我们利用 PMCA 技术,该技术可以检测到很少的 PrP(Sc)分子。我们的结果表明,外周给予的朊病毒直接到达大脑,尽管水平低于产生疾病所需的最低水平。给予后 PrP(Sc)在大脑中持续存在数天,表明清除效率低下或早期复制。了解给药后感染因子的命运及其在不同器官和液体中的摄取,可能为制定策略以最大程度减少朊病毒病的进一步传播提供有用信息。