Schlaepfer W W
J Neuropathol Exp Neurol. 1978 May;37(3):244-54. doi: 10.1097/00005072-197805000-00002.
Experimental structural alterations were studied in neurofilaments isolated from rat peripheral nerve. Structural alterations were induced in vitro by prolonged incubations of neurofilament-rich fractions in 0.1 M KCl prior to fixation and examination of neurofilaments by negative staining techniques. Neurofilaments appeared to retain their structural integrity during the first week of incubation. Subsequently, a progressive reduction in the numbers of intact neurofilaments coincided with the increasing appearance of neurofilamentous breakdown products. During the period of neurofilament breakdown, an increasing number of altered neurofilaments were observed. These abnormal neurofilaments were characterized primarily by axial enlargements with diameters frequently occurring in the 150-200 A range but measuring up to 250 A. Enlarged neurofilaments also showed a greater irregularity of their lateral margins and less ridigity in their linear course. A striking feature of enlarged neurofilaments was their tendency to display twisting deformations along their longitudinal axes. Twists occurred most frequently along neurofilaments of greatest diameter. The largest abnormal neurofilaments reveal multiple periodic twists, sometimes occurring at 800-1000 A intervals. These enlarged and twisted neurofilaments resembled the abnormal filaments described in neurofibrillary tangles and plaques. The demonstration of neurofilament plasticity as well as the resemblance of neurofilaments deformed in vitro to the abnormal filamentous structures of neurofibrillary tangles and plaques has led to the suggestion that the latter structures may be derived from alterations of normally-formed neurofilaments. Furthermore, it is proposed that the enlarged and twisted filaments of neurofibrillary pathology may arise from alterations in the turnover of neurofilaments or, more specifically, from deficiencies in the degradative processes by which these organelles are broken down.
对从大鼠外周神经分离出的神经丝中的实验性结构改变进行了研究。在固定并用负染色技术检查神经丝之前,通过将富含神经丝的组分在0.1M KCl中长时间孵育,在体外诱导结构改变。在孵育的第一周,神经丝似乎保持其结构完整性。随后,完整神经丝数量的逐渐减少与神经丝分解产物出现的增加相一致。在神经丝分解期间,观察到越来越多改变的神经丝。这些异常神经丝的主要特征是轴向增粗,直径通常在150 - 200埃范围内,但可达250埃。增粗的神经丝其侧缘也表现出更大的不规则性,并且在线性走行中刚性较小。增粗神经丝的一个显著特征是它们倾向于沿其纵轴显示扭曲变形。扭曲最常出现在直径最大的神经丝上。最大的异常神经丝显示出多个周期性扭曲,有时以800 - 1000埃的间隔出现。这些增粗和扭曲的神经丝类似于在神经原纤维缠结和斑块中描述的异常细丝。神经丝可塑性的证明以及体外变形的神经丝与神经原纤维缠结和斑块的异常丝状结构的相似性表明,后者的结构可能源自正常形成的神经丝的改变。此外,有人提出神经原纤维病变中增粗和扭曲的细丝可能源于神经丝周转的改变,或者更具体地说,源于这些细胞器分解的降解过程中的缺陷。