首页> 美国卫生研究院文献>Acta Neuropathologica Communications >Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature
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Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature

机译:白质中具有PrP淀粉样斑块的非典型Creutzfeldt-Jakob病:分子特征和向田鼠的传播显示M1菌株特征

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摘要

Amyloid plaques formed by abnormal prion protein (PrPSc) aggregates occur with low frequency in Creutzfeldt-Jakob disease, but represent a pathological hallmark of three relatively rare disease histotypes, namely variant CJD, sporadic CJDMV2K (methionine/valine at PRNP codon 129, PrPSc type 2 and kuru-type amyloid plaques) and iatrogenic CJDMMiK (MM at codon 129, PrPSc of intermediate type and kuru plaques). According to recent studies, however, PrP-amyloid plaques involving the subcortical and deep nuclei white matter may also rarely occur in CJDMM1 (MM at codon 129 and PrPSc type 1), the most common CJD histotype.To further characterize the phenotype of atypical CJDMM1 with white matter plaques (p-CJDMM1) and unravel the basis of amyloid plaque formation in such cases, we compared clinical and histopathological features and PrPSc physico-chemical properties between 5 p-CJDMM1 and 8 typical CJDMM1 brains lacking plaques. Furthermore, transmission properties after bioassay in two genetic lines of bank voles were also explored in the two groups.All 5 p-CJDMM1 cases had a disease duration longer than one year. Three cases were classified as sporadic CJDMM1, one as sporadic CJDMM1 + 2C and one as genetic CJDE200K-MM1. Molecular mass, protease sensitivity and thermo-solubilization of PrPSc aggregates did not differ between p-CJDMM1 and classical CJDMM1 cases. Likewise, transmission properties such as incubation time, lesion profile and PrPSc properties in bank voles also matched in the two groups.The present data further define the clinical-pathologic phenotype of p-CJDMM1, definitely establish it as a distinctive CJD histotype and demonstrate that PrP-plaque formation in this histotype is not a strain-specific feature. Since cases lacking amyloid plaques may also manifest a prolonged (i.e. > than one year) disease course, unidentified, host-specific factors likely play a significant role, in addition to disease duration, in generating white matter PrP-amyloid plaques in p-CJDMM1.Electronic supplementary materialThe online version of this article (10.1186/s40478-017-0496-7) contains supplementary material, which is available to authorized users.
机译:异常病毒蛋白(PrP Sc )聚集体形成的淀粉样斑块在Creutzfeldt-Jakob病中的发生频率较低,但代表了三种相对罕见的疾病组织学类型的病理学特征,即变种CJD,散发性CJDMV2K(蛋氨酸/缬氨酸在PRNP密码子129,PrP Sc 2型和kuru型淀粉样斑块和医源性CJDMMiK(MM在密码子129,PrP Sc 中间类型和kuru斑块中)。然而,根据最近的研究,涉及皮层下和深核白质的PrP淀粉样斑块也很少出现在CJDMM1中(MM密码子129和PrP Sc 1型),这是最常见的CJD组织型。为了进一步表征具有白质斑块(p-CJDMM1)的非典型CJDMM1的表型,并阐明这种情况下淀粉样斑块的形成基础,我们比较了两者之间的临床和组织病理学特征以及PrP Sc 的理化性质5个p-CJDMM1和8个典型的CJDMM1大脑缺乏斑块。此外,还在两组中探索了在生物测定后在两个银行田鼠遗传系中的传播特性。所有5个p-CJDMM1病例的病程都超过一年。其中三例为散发性CJDMM1,一类为散发性CJDMM1 ++ 2C,一类为遗传性CJDE200K-MM1。在p-CJDMM1病例和经典CJDMM1病例之间,PrP Sc 聚集体的分子量,蛋白酶敏感性和热增溶作用没有差异。同样,两组的潜伏期,潜伏期,病灶和PrP Sc 等传播特性也相匹配。目前的数据进一步定义了p-CJDMM1的临床病理表型,可以肯定地确定它的存在。作为独特的CJD组织型,并证明此组织型中的PrP斑块形成不是菌株特异性的特征。由于缺乏淀粉样斑块的病例也可能表现出病程延长(即大于一年),因此除疾病持续时间外,未知的宿主特异性因素在p-CJDMM1中产生白质PrP-淀粉样斑块中可能也起着重要作用。电子补充材料本文的在线版本(10.1186 / s40478-017-0496-7)包含补充材料,授权用户可以使用。

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