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Cell Surface N-Glycans Influence Electrophysiological Properties and Fate Potential of Neural Stem Cells

机译:细胞表面N-聚糖影响神经干细胞的电生理特性和命运

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Summary Understanding the cellular properties controlling neural stem and progenitor cell (NSPC) fate choice will improve their therapeutic potential. The electrophysiological measure whole-cell membrane capacitance reflects fate bias in the neural lineage but the cellular properties underlying membrane capacitance are poorly understood. We tested the hypothesis that cell surface carbohydrates contribute to NSPC membrane capacitance and fate. We found NSPCs differing in fate potential express distinct patterns of glycosylation enzymes. Screening several glycosylation pathways revealed that the one forming highly branched N-glycans differs between neurogenic and astrogenic populations of cells in?vitro and in?vivo . Enhancing highly branched N-glycans on NSPCs significantly increases membrane capacitance and leads to the generation of more astrocytes at the expense of neurons with no effect on cell size, viability, or proliferation. These data identify the N-glycan branching pathway as a significant regulator of membrane capacitance and fate choice in the neural lineage.
机译:总结了解控制神经干细胞和祖细胞(NSPC)命运选择的细胞特性将提高其治疗潜力。电生理学测量全细胞膜电容反映了神经谱系中的命运偏向,但对膜电容基础的细胞特性了解甚少。我们测试了细胞表面碳水化合物有助于NSPC膜电容和命运的假设。我们发现命运命运不同的NSPCs表达糖基化酶的不同模式。筛选了几种糖基化途径后发现,在体外和体内,神经源性细胞和星形细胞均会形成高度分支的N-聚糖。在NSPC上增强高度分支的N-聚糖可显着增加膜电容,并导致更多星形胶质细胞的生成,但会损害神经元,而对细胞大小,生存力或增殖没有影响。这些数据确定N-聚糖分支途径是神经系统中膜电容和命运选择的重要调节剂。

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