Md Rejaul Hoq, Anllely Fernandez, Frank S. Vago, Grace I. Hallinan, Sakshibeedu R. Bharath, Daoyi Li, Kadir A. Ozcan, Holly J. Garringer, Wen Jiang, Ruben Vidal, Bernardino Ghetti
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引用次数: 0
摘要
棉絮斑(CWPs)被描述为显性遗传性阿尔茨海默病(DIAD)神经病理学表型的特征,该病是由 Presenilin 1(PSEN1)基因的某些错义和缺失突变引起的。CWPs是缺乏淀粉样核心的圆形嗜酸性淀粉样-β(Aβ)斑块,在硫黄素S(ThS)制剂中可被识别,但无荧光。氨基酸末端截短和翻译后修饰的 Aβ 肽是 CWPs 的主要成分。CWPs 中可能存在 Tau 免疫阳性神经元。此外,神经纤维缠结也与 CWPs 共存。在此,我们报告了从因 PSEN1 V261I 和 A431E 突变导致的 DIAD 患者脑组织中分离出的 Aβ 和 tau 纤维的结构,这些患者具有 CWP 神经病理学表型。CWPs主要由I型Aβ丝组成,并以Ic型和Id型两种新的排列方式存在;此外,CWPs还含有I型和Ib型Aβ丝。Tau丝具有AD折叠,这在散发性AD和DIAD中已有报道。Ic 型和 Id 型 Aβ 细丝的形成可能是 CWPs 表型的基础。我们的数据与 PET 成像方法的发展相关,以最好地检测 DIAD 中的 CWPs。
Cryo-EM structures of cotton wool plaques’ amyloid β and of tau filaments in dominantly inherited Alzheimer disease
Cotton wool plaques (CWPs) have been described as features of the neuropathologic phenotype of dominantly inherited Alzheimer disease (DIAD) caused by some missense and deletion mutations in the presenilin 1 (PSEN1) gene. CWPs are round, eosinophilic amyloid-β (Aβ) plaques that lack an amyloid core and are recognizable, but not fluorescent, in Thioflavin S (ThS) preparations. Amino-terminally truncated and post-translationally modified Aβ peptide species are the main component of CWPs. Tau immunopositive neurites may be present in CWPs. In addition, neurofibrillary tangles coexist with CWPs. Herein, we report the structure of Aβ and tau filaments isolated from brain tissue of individuals affected by DIAD caused by the PSEN1 V261I and A431E mutations, with the CWP neuropathologic phenotype. CWPs are predominantly composed of type I Aβ filaments present in two novel arrangements, type Ic and type Id; additionally, CWPs contain type I and type Ib Aβ filaments. Tau filaments have the AD fold, which has been previously reported in sporadic AD and DIAD. The formation of type Ic and type Id Aβ filaments may be the basis for the phenotype of CWPs. Our data are relevant for the development of PET imaging methodologies to best detect CWPs in DIAD.
期刊介绍:
Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.