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首页> 外文期刊>Cell structure and function >Evidence for Direct Binding of Intracellularly Distributed Ganglioside GM2 to Isolated Vimentin Intermediate Filaments in Normal and Tay-Sachs Disease Human Fibroblasts
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Evidence for Direct Binding of Intracellularly Distributed Ganglioside GM2 to Isolated Vimentin Intermediate Filaments in Normal and Tay-Sachs Disease Human Fibroblasts

机译:正常和Tay-Sachs病人类成纤维细胞中胞内分布神经节苷脂GM2与孤立波形蛋白中间丝的直接结合的证据。

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References(40) Cited-By(9) Although some intracellularly distributed glycosphingolipids are reported to be associated with vimentin intermediate filaments or colchicine sensitive cytoskeleton, no direct evidence for such an association has yet been shown. In this report we demonstrated that the intracellularly distributed ganglioside GM2 directly binds to isolated vimentin intermediate filaments in normal and Tay-Sachs disease human fibroblasts. Indirect immunofluorescence microscopy using a GM2-specific monoclonal antibody demonstrated filamentously distributed GM2 in the cytoplasm. A double staining of Tay-Sachs fibroblasts with anti-GM2 and anti-vimentin monoclonal antibodies strongly suggested that the GM2 positive filaments are vimentin intermediate filaments. We then isolated vimentin, in the presence of a detergent and urea, from the normal human skin fibroblasts and murine mastocytoma cells. In a solid phase enzyme-linked immunosorbent assay, the isolated vimentin dose-dependently reacted with both anti-vimentin and anti-GM2 monoclonal antibodies but not with anti-GM3 or anti-GM1 monoclonal antibody. The molar ratio of GM2 to vimentin was approximately 20 : 1. The lipid fraction extracted from the purified vimentin preparation was immunostained with anti-GM2 on a thin-layer chromatography plate. Furthermore, only one band was detected at the molecular weight of 57 kDa, after electroblotting and simultaneous immunostaining with anti-GM2 and anti-vimentin monoclonal antibodies. These results clearly indicated that ganglioside GM2 directly binds to vimentin.
机译:参考文献(40)被引用的(9)尽管一些细胞内分布的鞘糖脂据报道与波形蛋白中间丝或秋水仙碱敏感的细胞骨架有关,但尚未显示出这种关联的直接证据。在此报告中,我们证明了在正常人和Tay-Sachs病患者的成纤维细胞中,细胞内分布的神经节苷脂GM2直接与分离的波形蛋白中间丝结合。使用GM2特异性单克隆抗体的间接免疫荧光显微镜检查证明GM2呈丝状分布在细胞质中。用抗GM2和抗波形蛋白单克隆抗体对Tay-Sachs成纤维细胞进行双重染色,强烈提示GM2阳性丝是波形蛋白中间丝。然后,在洗涤剂和尿素存在的情况下,我们从正常人的皮肤成纤维细胞和鼠肥大细胞瘤细胞中分离了波形蛋白。在固相酶联免疫吸附试验中,分离的波形蛋白与抗波形蛋白和抗GM2单克隆抗体呈剂量依赖性反应,但不与抗GM3或抗GM1单克隆抗体发生反应。 GM2与波形蛋白的摩尔比为约20∶1。将从纯化的波形蛋白制剂中提取的脂质级分在薄层色谱板上用抗GM2免疫染色。此外,在用抗GM2和抗波形蛋白单克隆抗体进行电印迹和同时免疫染色后,仅以57 kDa的分子量检测到一个条带。这些结果清楚地表明神经节苷脂GM2直接结合波形蛋白。

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