首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Expanding morphological dimensions in neuropathology, from sequence biology to pathological sequences and clinical consequences.
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Expanding morphological dimensions in neuropathology, from sequence biology to pathological sequences and clinical consequences.

机译:从序列生物学到病理序列和临床后果,神经病理学的形态学范围不断扩大。

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摘要

One of the challenges in neuropathology is to clarify how molecules, functional carriers of uni-dimensional sequence of amino acid or nucleic acid, behave to engender disease-specific pathological processes in complex three-dimensional (3D) structures such as the human brain in an ordered chronological sequence (four-dimensional extension as a whole). Along with expanding molecular explanations for brain diseases, parallel and independent hypotheses based on morphological observations are particularly useful and necessary for reasonable understanding of the brain and its dysfunction. For example, with classical methods such as silver impregnations, it is possible to differentiate underlying molecular pathologies (three-repeat tau/Campbell-Switzer vs. four-repeat tau/Gallyas silver impregnation) for improved histological diagnosis. Innovations with 3D reconstruction not only provide more realistic reproduction of the targets but also allow quantitative measurement on a 3D basis (3D volumetry). Contrary to the prevailing impression that pathological deposits are generally toxic to cells, quantification demonstrated possible countertoxic potentials of ubiquitin-positive intranuclear inclusions in CAG-repeat disorders on a two-dimensional basis and of glial cytoplasmic inclusions of multiple system atrophy on 3D volumetry. Furthermore, 3D extension of neurites around target lesions is now traceable in relation to the relevant clinical consequences. This neurite neuropathology may pave the way for early specific diagnosis of neurodegenerative disorders, as established through (123) I-metaiodobenzylguanidine cardiac scintigraphy for Parkinson disease, aiming at therapeutic intervention before depletion of mother neurons is feasible. For appropriate translation of sequence biology into the frame of human neuropathology, it is necessary to expand further the morphological dimensions so that comprehensive understanding of these disorders leads to specific diagnosis and treatment as early as possible.
机译:神经病理学的挑战之一是弄清氨基酸或核酸一维序列的功能性载体分子如何在复杂的三维(3D)结构(如人脑)中引发特定于疾病的病理过程。有序的时间顺序(整体为四维扩展)。除了扩展对脑疾病的分子解释外,基于形态学观察的平行和独立假设对于合理理解大脑及其功能障碍特别有用,而且是必要的。例如,使用银浸渍等经典方法,可以区分潜在的分子病理学(三重复tau / Campbell-Switzer与四重复tau / Gallyas银浸渍),以改善组织学诊断。 3D重建的创新不仅可以更真实地再现目标,还可以在3D基础上进行定量测量(3D体积测量)。与普遍认为病理性沉积物通常对细胞有毒的印象相反,定量分析显示二维基础上CAG重复性疾病中泛素阳性核内包涵体和3D容积法中多系统萎缩的神经胶质细胞质包涵体可能具有抗毒潜力。此外,与相关的临床后果相关的神经突在目标病灶周围的3D延伸现已可追溯。这种神经突神经病理学可能为神经退行性疾病的早期特异性诊断铺平道路,这是通过针对帕金森病的(123)I-甲氧代苄基胍心脏闪烁显像技术建立的,旨在在可行的母体神经元耗竭之前进行治疗性干预。为了将序列生物学适当翻译成人神经病理学框架,有必要进一步扩大形态学的范围,以便对这些疾病的全面了解可以尽早进行具体的诊断和治疗。

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