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Immunohistochemical and biochemical analyses of GD3, GT1b, and GQ1b gangliosides during neural differentiation of P19 EC cells 1

机译:P19 EC 细胞神经分化过程中 GD3、GT1b 和 GQ1b 神经节苷脂的免疫组织化学和生化分析 1

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In an earlier study, we showed that expressions of GD3, GT1b, and GQ1b gangliosides in P19 embryonic carcinoma (EC) cells were enhanced during their neural differentiation induced by retinoic acid. We now further demonstrated that this increase of the b-series gangliosides is due to an increase in their corresponding synthases (sialyltransferase-II, -IV, and -V) in the Golgi. Of the three gangliosides studied, GQ1b appeared to be the best candidate for monitoring such differentiation process. We also used fluorescence-labeled monoclonal antibodies and confocal fluorescence microscopy to obtain direct visual information about the relationship of gangliosides and neural specific proteins in neuron development. Again, GQ1b is the most interesting as it localizes with synaptophysin and neural cell adhesion molecules (NCAMs) on synaptic boutons or dendritic spines in RA-induced neurons (R/N). This suggests that GQ1b could be used as a marker for synapse formation during construction of the neural network.
机译:在早期的一项研究中,我们发现 P19 胚胎癌 (EC) 细胞中 GD3、GT1b 和 GQ1b 神经节苷脂的表达在视黄酸诱导的神经分化过程中得到增强。我们现在进一步证明,b系列神经节苷脂的这种增加是由于高尔基体中相应的合酶(唾液酸转移酶-II,-IV和-V)的增加。在所研究的三种神经节苷脂中,GQ1b似乎是监测这种分化过程的最佳候选者。我们还使用荧光标记的单克隆抗体和共聚焦荧光显微镜来获得有关神经元发育中神经节苷脂和神经特异性蛋白关系的直接视觉信息。同样,GQ1b 是最有趣的,因为它与突触素和神经细胞粘附分子 (NCAM) 一起定位在 RA 诱导的神经元 (R/N) 的突触布顿或树突棘上。这表明GQ1b可以用作神经网络构建过程中突触形成的标志物。

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