Gennarini G, Durbec P, Boned A, Rougon G, Goridis C
Centre d'Immunologie, INSERM-CNRS de Marseille-Luminy, France.
Neuron. 1991 Apr;6(4):595-606. doi: 10.1016/0896-6273(91)90062-5.
The mouse neuronal F3 glycoprotein and its chicken homolog F11 belong to a subclass of proteins of the immunoglobulin superfamily with preferential localization on axons and neurites. We have transfected F3 cDNA into CHO cells. Biochemical analysis establishes that the cDNA we have cloned codes for a 130 kd phosphatidylinositol-anchored polypeptide. F3-expressing transfectants exhibited enhanced self-adhesive properties, aggregating with faster kinetics and forming larger aggregates than F3-negative control cells. When used as a culture substrate for sensory neurons, F3-transfected cells showed a markedly enhanced ability to promote neurite outgrowth compared with nontransfected cells. The results support the idea that F3/F11 and other closely similar proteins function as cell adhesion molecules that play a role in axonal growth and guidance.
小鼠神经元F3糖蛋白及其鸡同源物F11属于免疫球蛋白超家族的一个蛋白质亚类,优先定位于轴突和神经突上。我们已将F3 cDNA转染到CHO细胞中。生化分析表明,我们克隆的cDNA编码一种130 kd的磷脂酰肌醇锚定多肽。表达F3的转染细胞表现出增强的自黏附特性,与F3阴性对照细胞相比,聚集动力学更快,形成的聚集体更大。当用作感觉神经元的培养底物时,与未转染细胞相比,F3转染细胞促进神经突生长的能力明显增强。这些结果支持了F3/F11和其他密切相似的蛋白质作为细胞黏附分子在轴突生长和导向中起作用的观点。