Debus E, Flügge G, Weber K, Osborn M
EMBO J. 1982;1(1):41-5. doi: 10.1002/j.1460-2075.1982.tb01121.x.
A mouse monoclonal antibody, designated NF1, was obtained from a cloned hybridoma isolated from a fusion of mouse myeloma Sp2 cells with spleen cells from a BALB/c mouse immunized with a crude neurofilament preparation from porcine spinal cord. NF1 is an IgG1 and recognizes, in immune blotting procedures, only the 200 K neurofilament triplet component. Its neurofilament-specific nature is further revealed by immunofluorescence microscopy studies on frozen tissue sections and various cultured cells. Immunoelectron microscopy studies on cytoskeletons of cultured neurones emphasize the discontinuous display along each neurofilament previously observed with polyclonal antibodies specific for the 200 K component after appropriate but rather cumbersome cross-absorption steps. Use of NF1 on various neuronal cells strongly supports the previous proposal of the existence of certain subpopulations of neurofilament-free neurones and the observation that certain neuronal arrangements, (e.g., those in dendrites of pyramidal cells of the hippocampus), although rich in neurofilaments, probably lack the normal 200 K triplet component. Since NF1 shows a broad cross-species reactivity and is able to react on formaldehyde-fixed tissue, it should be a useful reagent to study differential neurofilament expression and organization in embryonic, adult and pathological tissues.
一种名为NF1的小鼠单克隆抗体,是从一个克隆的杂交瘤中获得的,该杂交瘤是由小鼠骨髓瘤Sp2细胞与用猪脊髓粗制神经丝制剂免疫的BALB/c小鼠的脾细胞融合而成。NF1是一种IgG1,在免疫印迹实验中,它仅识别200K的神经丝三联体成分。对冷冻组织切片和各种培养细胞进行免疫荧光显微镜研究,进一步揭示了其神经丝特异性。对培养神经元的细胞骨架进行免疫电子显微镜研究,强调了在经过适当但相当繁琐的交叉吸收步骤后,先前用针对200K成分的多克隆抗体观察到的沿每条神经丝的不连续显示。在各种神经元细胞上使用NF1,有力地支持了先前关于存在某些无神经丝神经元亚群的提议,以及关于某些神经元排列(例如海马锥体细胞树突中的排列)尽管富含神经丝,但可能缺乏正常200K三联体成分的观察结果。由于NF1显示出广泛的跨物种反应性,并且能够与甲醛固定的组织发生反应,因此它应该是研究胚胎、成年和病理组织中神经丝差异表达和组织的有用试剂。