Pesheva P, Gennarini G, Goridis C, Schachner M
Department of Neurobiology, Swiss Federal Institute of Technology, Zürich.
Neuron. 1993 Jan;10(1):69-82. doi: 10.1016/0896-6273(93)90243-k.
The oligodendrocyte-derived extracellular matrix protein J1-160/180 displays repellent substrate properties toward neurons. In a search for neuronal ligands mediating the response to J1-160/180, we have identified the F3/11 cell surface protein, a glyco-phosphatidylinositol-anchored member of the immunoglobulin superfamily. F3/11 mediates the initial recognition between a J1-160/180 substrate and cerebellar neurons or F3-transfected CHO cells. In cerebellar neurons, the F3/11-J1-160/180 interaction induces a repulsion consisting of the loss of substrate adhesion with time in culture and inhibition of neurite outgrowth. Antibody blocking experiments show that the avoidance response of neurites at J1-160/180 substrate borders is also mediated by F3/11. Active cell-cell and cell-substrate repulsion is considered a major mechanism governing the extent and directionality of axonal growth, but the ligand-receptor interactions involved have remained unknown. Our results show that F3/11 mediates the neuronal response to the repellent molecule J1-160/180 and may thus be involved in signal transduction leading to cell repulsion.
少突胶质细胞衍生的细胞外基质蛋白J1-160/180对神经元具有排斥性底物特性。在寻找介导对J1-160/180反应的神经元配体的过程中,我们鉴定出了F3/11细胞表面蛋白,它是免疫球蛋白超家族中糖基磷脂酰肌醇锚定的成员。F3/11介导了J1-160/180底物与小脑神经元或F3转染的CHO细胞之间的初始识别。在小脑神经元中,F3/11-J1-160/180相互作用诱导了一种排斥反应,表现为随着培养时间的推移底物附着力丧失以及神经突生长受到抑制。抗体阻断实验表明,神经突在J1-160/180底物边界处的回避反应也由F3/11介导。活跃的细胞间和细胞与底物间的排斥被认为是控制轴突生长范围和方向性的主要机制,但其中涉及的配体-受体相互作用仍不清楚。我们的结果表明,F3/11介导了神经元对排斥分子J1-160/180的反应,因此可能参与了导致细胞排斥的信号转导。