Clarke G A, White C A, Moss D J
Department of Human Anatomy and Cell Biology, University of Liverpool, United Kingdom.
Eur J Cell Biol. 1993 Jun;61(1):108-15.
GP130/F11 is a neuronal cell adhesion molecule belonging to the Ig superfamily. Preliminary evidence suggests that it may be important for the fasciculation of axons and cell-cell interactions during synaptogenesis. Previous work has shown that when F3 (the mouse homologue) is transfected into Chinese hamster ovary (CHO) cells it will act as a substrate for neuronal growth and adhesion. In this study we have shown that isolated GP130/F11 will also act as a substrate for the growth of chick dorsal root ganglia cell neurons. The concentration of GP130/F11 on the surface of sympathetic neurons, grown for one day in culture was approximately 40 ng cm-2 which was comparable to the levels required to stimulate neurite outgrowth. Deglycosylation of GP130/F11 or partial denaturation by boiling did not abolish the activity. However, after treatment with dithiothreitol, GP130/F11 was no longer capable of stimulating neurite outgrowth. GP130/F11 will also stimulate neurite outgrowth from forebrain neurons from 7 to 9-day-old embryos. These do not express GP130/F11 until around day 10, providing further evidence that GP130/F11 interacts with an as yet unknown cell surface receptor.
GP130/F11是一种属于免疫球蛋白超家族的神经元细胞粘附分子。初步证据表明,它可能在轴突成束和突触形成过程中的细胞间相互作用中起重要作用。先前的研究表明,当将F3(小鼠同源物)转染到中国仓鼠卵巢(CHO)细胞中时,它将作为神经元生长和粘附的底物。在本研究中,我们表明分离的GP130/F11也将作为鸡背根神经节细胞神经元生长的底物。在培养中生长一天的交感神经元表面上GP130/F11的浓度约为40 ng/cm²,这与刺激神经突生长所需的水平相当。GP130/F11的去糖基化或通过煮沸进行的部分变性并没有消除其活性。然而,用二硫苏糖醇处理后,GP130/F11不再能够刺激神经突生长。GP130/F11也将刺激7至9天大胚胎的前脑神经元的神经突生长。这些神经元直到大约第10天才表达GP130/F11,这进一步证明GP130/F11与一种尚未知的细胞表面受体相互作用。