Ksiezak-Reding H, Tracz E, Yang L S, Dickson D W, Simon M, Wall J S
Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
Am J Pathol. 1996 Aug;149(2):639-51.
Paired helical filaments (PHFs) accumulate in the brains of subjects affected with Alzheimer's disease (AD) and certain other neurodegenerative disorders, including corticobasal degeneration (CBD). Electron microscope studies have shown that PHFs from CBD differ from those of AD by being wider and having a longer periodicity of the helical twist. Moreover, PHFs from CBD have been shown to be primarily composed of two rather than three highly phosphorylated polypeptides of tau (PHF-tau), with these polypeptides expressing no exons 3 and 10. To further explore the relationship between the heterogeneity of PHF-tau and the appearance of abnormal filaments, the ultrastructure and physical parameters such as mass per unit length and dimensions were compared in filaments from CBD and AD using high resolution scanning transmission electron microscopy (STEM). Filament-enriched fractions were isolated as Sarcosyl-insoluble pellets and for STEM studies, samples were freeze-dried without prior fixation or staining. Ultrastructurally, PHFs from CBD were shown to be a heterogeneous population as double- and single-stranded filaments could be identified based on their width and physical mass per unit length expressed in kilodaltons (kd) per nanometer (nm). Less abundant, double-stranded filaments had a maximal width of 29 nm and a mass per unit length of 133 kd/nm, whereas three times more abundant single-stranded filaments were 15 nm wide and bad a mass per unit length of 62 kd/nm. Double-stranded filaments also displayed a distinct axial region of less dense mass, which appeared to divide the PHFs into two protofilament-like strands. Furthermore, these filaments were frequently observed to physically separate along the long axis into two single strands or to break longitudinally. In contrast, PHFs from AD were ultrastructurally stable and uniform both in their width (22 nm) and physical mass per unit length (104 kd/nm). The ultrastructural features indicate that filaments of CBD and AD differ both in stability and packing of tau and that CBD filaments, composed of two distinct protofilaments, are more labile under STEM conditions. As fixed and stained filaments from CBD have been shown to be stable and uniform in size by conventional transmission electron microscopy, STEM studies may be particularly suitable for detecting instability of unstained and unfixed filaments. The results also suggest that molecular heterogeneity and/or post-translational modifications of tau may strongly influence the morphology and stability of abnormal filaments.
成对螺旋丝(PHFs)在患有阿尔茨海默病(AD)以及某些其他神经退行性疾病(包括皮质基底节变性,CBD)的患者大脑中蓄积。电子显微镜研究表明,CBD的PHFs与AD的PHFs不同,前者更宽,螺旋扭曲的周期更长。此外,已证明CBD的PHFs主要由两种而非三种高度磷酸化的tau多肽(PHF-tau)组成,这些多肽不表达外显子3和10。为了进一步探究PHF-tau的异质性与异常细丝出现之间的关系,使用高分辨率扫描透射电子显微镜(STEM)对CBD和AD细丝的超微结构以及诸如单位长度质量和尺寸等物理参数进行了比较。富含细丝的组分被分离为十二烷基肌氨酸钠不溶性沉淀,用于STEM研究的样品未经预先固定或染色直接进行冷冻干燥。在超微结构上,CBD的PHFs显示为异质群体,根据其宽度和以千道尔顿(kd)每纳米(nm)表示的单位长度物理质量,可以识别出双链和单链细丝。数量较少的双链细丝最大宽度为29 nm,单位长度质量为133 kd/nm,而数量多三倍的单链细丝宽15 nm,单位长度质量为62 kd/nm。双链细丝还显示出一个明显的轴向低密度区域,该区域似乎将PHFs分为两条原丝样链。此外,经常观察到这些细丝沿长轴在物理上分离为两条单链或纵向断裂。相比之下,AD的PHFs在超微结构上稳定且均匀,宽度为22 nm,单位长度物理质量为104 kd/nm。超微结构特征表明,CBD和AD的细丝在tau的稳定性和堆积方面均存在差异,并且由两条不同原丝组成的CBD细丝在STEM条件下更不稳定。由于传统透射电子显微镜已显示CBD的固定和染色细丝在大小上稳定且均匀,STEM研究可能特别适合检测未染色和未固定细丝的不稳定性。结果还表明,tau的分子异质性和/或翻译后修饰可能强烈影响异常细丝的形态和稳定性。