Drescher U, Kremoser C, Handwerker C, Löschinger J, Noda M, Bonhoeffer F
Max-Planck-Institute for Developmental Biology, Department of Physical Biology, Tübingen, Federal Republic of Germany.
Cell. 1995 Aug 11;82(3):359-70. doi: 10.1016/0092-8674(95)90425-5.
The results of previous in vitro experiments indicate that a glycosylphosphatidylinositol (GPI)-anchored protein may play an important role in the guidance of temporal retinal axons during the formation of the topographically ordered retinotectal projection. We have purified and cloned a GPI-anchored, 25 kDa glycoprotein that is a good candidate for a molecule involved in this process. During the time of innervation by retinal ganglion cells, this protein is gradedly expressed in the posterior part of the developing tectum. In two different in vitro assay systems, the recombinant protein induces growth cone collapse and repulsion of retinal ganglion cell axons. These phenomena are observed for axons of temporal as well as nasal origin, indicating that an additional activity may be necessary to confer the nasotemporal specificity observed in previous assays. We named the protein RAGS (for repulsive axon guidance signal). The sequence of RAGS shows significant homology to recently identified ligands for receptor tyrosine kinases of the Eph subfamily.
先前的体外实验结果表明,糖基磷脂酰肌醇(GPI)锚定蛋白可能在形成拓扑有序的视网膜 - 脑顶盖投射过程中,对视网膜轴突的时间导向起重要作用。我们已经纯化并克隆了一种GPI锚定的25 kDa糖蛋白,它是参与这一过程的分子的良好候选者。在视网膜神经节细胞支配期间,这种蛋白在发育中的脑顶盖后部逐渐表达。在两种不同的体外检测系统中,重组蛋白诱导视网膜神经节细胞轴突的生长锥塌陷和排斥。在颞侧以及鼻侧起源的轴突中均观察到这些现象,这表明可能需要额外的活性才能赋予先前检测中观察到的鼻颞特异性。我们将该蛋白命名为RAGS(排斥性轴突导向信号)。RAGS的序列与最近鉴定的Eph亚家族受体酪氨酸激酶的配体具有显著同源性。