Manuelidis L, Manuelidis E E
J Neurocytol. 1976 Oct;5(8):575-89. doi: 10.1007/BF01175571.
Cholera toxin was coupled to peroxidase to yield a highly specific marker for GM1 gangliosides. Study of embryonic brain cells in culture revealed intense binding of cholera-peroxidase by plasma membranes of both neurons and glial cells. In contrast, long-term monolayer glioblastoma cultures, including one producing C-type virus, revealed virtually no labelling of their plasma membranes. Such cells were shown to be capable of incorporating exogenously applied GM1 into their plasma membranes. Studies with fixed brain and synaptosomal fractions were in accord with results on embryonic brain cells in culture, and autoradiographic findings with 125I cholera supported observations made utilizing cholera-peroxidase. From our studies there is some indication that long-term propagation in vitro alters the plasma membrane GM1.
霍乱毒素与过氧化物酶偶联,产生一种针对GM1神经节苷脂的高度特异性标记物。对培养的胚胎脑细胞的研究表明,神经元和胶质细胞的质膜对霍乱-过氧化物酶有强烈的结合。相比之下,长期单层培养的胶质母细胞瘤细胞,包括一种产生C型病毒的细胞,其质膜几乎没有标记。这些细胞被证明能够将外源施加的GM1整合到它们的质膜中。对固定的脑和突触体组分的研究与培养的胚胎脑细胞的结果一致,并且用125I霍乱进行的放射自显影结果支持了利用霍乱-过氧化物酶所做的观察。从我们的研究中有一些迹象表明,体外长期传代会改变质膜GM1。