与129MV基因型相关的散发性克雅氏病的新组织类型。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Laura Cracco, Gianfranco Puoti, Antonio Cornacchia, Katie Glisic, Seong-Ki Lee, Zerui Wang, Mark L Cohen, Brian S Appleby, Ignazio Cali
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引用次数: 0

摘要

散发性克雅氏病(sCJD)的MV1和MV2亚型与朊病毒蛋白(PrP)基因第129密码子处的杂合甲硫氨酸(M)/缬氨酸(V)多态性有关。MV2在表型上是异质性的,而MV1由于其低患病率,是特征最不明确的亚型之一。在本研究中,我们研究了PrPSc的生化特性以及被诊断为sCJD MV1和MV2的病例的表型表达。我们描述了四种MV2组织类型:2C,皮质(C)粗糙病理;2K,具有kuru(K)斑块沉积物;2C-K,具有共存的C和K组织型特征;以及新的组织型2C-PL,其在大脑皮层和小脑中模拟2C,但在皮层下区域(例如,基底核、丘脑和中脑)中表现出斑块状(PL)PrP沉积。2C-K的组织型患病率最高(55%),2C中等(31%),2C-PL和2K最低(7%)。几乎每个MV2病例都表达两种PrPSc类型,其中T2是主要类型(“MV2-1”)。MV1病例通常表现为快速病程(≤ 4个月),并具有1C组织型,表型与sCJDMM1相同。在病程较长的MV1患者中检测到共存的PrPSc类型,T1显著超过T2(“MV1-2”)。我们在MV1-2病例中观察到四种组织类型,包括两种新的组织类型:1V,让人想起sCJDVV1;1C-2C,类似于sCJDMM1-2,具有主要的MM1组织型成分;以及新的组织类型1C-2PL和1C-2K,总体上模仿大脑皮层中的1C,但在皮层下区域(1C-2PL)中含有T2和斑块状PrP沉积,在小脑中含有T2斑块和kuru斑块(1C-2K)。1C、1V和1C-2C的病变情况相似,但与1C-2PL和1C-2K不同,因为后两组显示出明显的海马和黑质变性。我们认为,新的“C-PL”组织型是“C”组和“C-K”组之间的不同实体,而不是中间形式,1C-2PL和1C-2K组织型的特征可能是相同大小的不同T1变体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype.

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype.

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype.

Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype.

The MV1 and MV2 subtypes of sporadic Creutzfeldt-Jakob disease (sCJD) are linked to the heterozygous methionine (M)/valine (V) polymorphism at codon 129 of the prion protein (PrP) gene. MV2 is phenotypically heterogeneous, whereas MV1, due to its low prevalence, is one of the least well characterized subtypes. In this study, we investigated the biochemical properties of PrPSc and phenotypic expression of cases diagnosed as sCJD MV1 and MV2. We describe four MV2 histotypes: 2C, with cortical (C) coarse pathology; 2K, with kuru (K) plaque deposits; 2C-K, with co-existing C and K histotypic features; and the novel histotype 2C-PL that mimics 2C in the cerebral cortex and cerebellum, but exhibits plaque-like (PL) PrP deposits in subcortical regions (e.g., basal nuclei, thalamus and midbrain). Histotype prevalence is highest for 2C-K (55%), intermediate for 2C (31%), and lowest for 2C-PL and 2K (7%). Nearly every MV2 case expressed both PrPSc types, with T2 being the predominant type ("MV2-1"). MV1 cases typically show a rapid disease course (≤ 4 months), and feature the 1C histotype, phenotypically identical to sCJDMM1. Co-existing PrPSc types, with T1 significantly exceeding T2 ("MV1-2"), are detected in patients diagnosed as MV1 with longer disease courses. We observed four histotypes among MV1-2 cases, including two novel histotypes: 1V, reminiscent of sCJDVV1; 1C-2C, resembling sCJDMM1-2 with predominant MM1 histotypic component; and novel histotypes 1C-2PL and 1C-2K, overall mimicking 1C in the cerebral cortex, but harboring T2 and plaque-like PrP deposits in subcortical regions (1C-2PL), and T2 and kuru plaques in the cerebellum (1C-2K). Lesion profiles of 1C, 1V, and 1C-2C are similar, but differ from 1C-2PL and 1C-2K, as the latter two groups show prominent hippocampal and nigral degeneration. We believe that the novel "C-PL" histotypes are distinct entities rather than intermediate forms between "C" and "C-K" groups, and that 1C-2PL and 1C-2K histotypes may be characterized by different T1 variants of the same size.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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