Miller C C, Brion J P, Calvert R, Chin T K, Eagles P A, Downes M J, Flament-Durand J, Haugh M, Kahn J, Probst A
EMBO J. 1986 Feb;5(2):269-76. doi: 10.1002/j.1460-2075.1986.tb04209.x.
A panel of monoclonal antibodies to neurofilaments have been investigated with regard to the location of their respective epitopes on neurofilament polypeptides and their ability to label the neurofibrillary tangles and paired helical filaments (PHF) which are characteristic of Alzheimer's disease. All of the neurofilament monoclonal antibodies that label tangles and PHF are directed against epitopes in the side arm domains of the two larger neurofilament polypeptides, NF-H and NF-M, and do not recognise the alpha-helical rod domains of these proteins. Immuno-electron microscopy demonstrates that the neurofilament antibodies label the constituent PHF per se and do not simply stain neurofilaments that might be admixed with PHF. These neurofilament epitopes are differentially retained by PHF, following isolation. Thus, antibody labelling of PHF is not simply due to the presence of normal neurofilament polypeptides. We propose that in tangle-bearing neurons, neurofilaments are degraded by proteases and that it is fragments of the side arms which contribute to the composition of PHF.
一组针对神经丝的单克隆抗体已针对其各自的表位在神经丝多肽上的位置以及它们标记神经原纤维缠结和双螺旋丝(PHF)的能力进行了研究,而神经原纤维缠结和双螺旋丝是阿尔茨海默病的特征。所有标记缠结和PHF的神经丝单克隆抗体均针对两种较大的神经丝多肽NF-H和NF-M的侧臂结构域中的表位,并且不识别这些蛋白质的α-螺旋杆状结构域。免疫电子显微镜显示,神经丝抗体标记了PHF本身的组成成分,而不仅仅是对可能与PHF混合的神经丝进行染色。这些神经丝表位在分离后被PHF差异保留。因此,PHF的抗体标记不仅仅是由于正常神经丝多肽的存在。我们提出,在带有缠结的神经元中,神经丝被蛋白酶降解,并且是侧臂的片段构成了PHF的组成成分。