Biffiger K, Bartsch S, Montag D, Aguzzi A, Schachner M, Bartsch U
Institute for Neurobiology, Federal Institute of Technology, Hönggerberg, CH-8093 Zürich, Switzerland.
J Neurosci. 2000 Oct 1;20(19):7430-7. doi: 10.1523/JNEUROSCI.20-19-07430.2000.
The analysis of mice deficient in the myelin-associated glycoprotein (MAG) or Fyn, a nonreceptor-type tyrosine kinase proposed to act as a signaling molecule downstream of MAG, has revealed that both molecules are involved in the initiation of myelination. To obtain more insights into the role of the MAG-Fyn signaling pathway during initiation of myelination and formation of morphologically intact myelin sheaths, we have analyzed optic nerves of MAG-, Fyn- and MAG/Fyn-deficient mice. We observed a slight hypomyelination in optic nerves of MAG mutants that was significantly increased in Fyn mutants and massive in MAG/Fyn double mutants. The severe morphological phenotype of MAG/Fyn mutants, accompanied by behavioral deficits, substantiates the importance of both molecules for the initiation of myelination. The different severity of the phenotype of different genotypes indicates that the MAG-Fyn signaling pathway is complex and suggests the presence of compensatory mechanisms in the single mutants. However, data are also compatible with the possibility that MAG and Fyn act independently to initiate myelination. Hypomyelination of optic nerves was not related to a loss of oligodendrocytes, indicating that the phenotype results from impaired interactions between oligodendrocyte processes and axons and/or impaired morphological maturation of oligodendrocytes. Finally, we demonstrate that Fyn, unlike MAG, is not involved in the formation of ultrastructurally intact myelin sheaths.
对髓鞘相关糖蛋白(MAG)或Fyn基因缺陷小鼠的分析表明,这两种分子都参与了髓鞘形成的起始过程。Fyn是一种非受体型酪氨酸激酶,被认为是MAG下游的信号分子。为了更深入了解MAG - Fyn信号通路在髓鞘形成起始和形态完整的髓鞘形成过程中的作用,我们分析了MAG、Fyn和MAG/Fyn基因缺陷小鼠的视神经。我们观察到,MAG突变体的视神经有轻微的髓鞘形成不足,在Fyn突变体中显著增加,而在MAG/Fyn双突变体中则大量存在。MAG/Fyn突变体严重的形态学表型,伴有行为缺陷,证实了这两种分子对髓鞘形成起始的重要性。不同基因型表型的不同严重程度表明,MAG - Fyn信号通路是复杂的,并提示单个突变体中存在补偿机制。然而,数据也与MAG和Fyn独立作用启动髓鞘形成的可能性相符。视神经的髓鞘形成不足与少突胶质细胞的丢失无关,这表明该表型是由于少突胶质细胞突起与轴突之间的相互作用受损和/或少突胶质细胞的形态成熟受损所致。最后,我们证明,与MAG不同,Fyn不参与超微结构完整的髓鞘形成。