Ciossek T, Monschau B, Kremoser C, Löschinger J, Lang S, Müller B K, Bonhoeffer F, Drescher U
Max-Planck-Institute for Developmental Biology, Department of Physical Biology, Tübingen, Germany.
Eur J Neurosci. 1998 May;10(5):1574-80. doi: 10.1046/j.1460-9568.1998.00180.x.
Previous results of an in vitro guidance test, the stripe assay, have demonstrated the presence of a repulsive axon guidance activity for temporal retinal axons in the posterior part of the vertebrate optic tectum. Ephrin-A5 and Ephrin-A2 are ligands for the EphA subfamily of Eph receptor tyrosine kinases, which are expressed in overlapping gradients in the posterior part of the tectum. When recombinantly expressed, both proteins have been shown to guide retinal ganglion cell axons in the stripe assay. While these results suggest that Ephrin-A5 and Ephrin-A2 form part of the posterior repulsive guidance activity, they do not elucidate whether they are necessary components. Here we report that soluble forms of the ligands at nanomolar concentrations completely abolish this repulsive activity. Similar results were obtained with the soluble extracellular domain of EphA3, which is a receptor for Ephrin-A2 and Ephrin-A5, but not with the corresponding domain of EphB3, a receptor for the transmembrane class of Eph ligands. These experiments show that the repulsive axon guidance activity seen in the stripe assay is mediated by Ephrin-A ligands.
先前一项体外导向试验(条纹试验)的结果表明,在脊椎动物视顶盖后部存在对颞侧视网膜轴突的排斥性轴突导向活性。Ephrin-A5和Ephrin-A2是Eph受体酪氨酸激酶EphA亚家族的配体,它们在视顶盖后部以重叠梯度表达。重组表达时,这两种蛋白在条纹试验中均已显示可引导视网膜神经节细胞轴突。虽然这些结果表明Ephrin-A5和Ephrin-A2构成了后部排斥性导向活性的一部分,但并未阐明它们是否为必需成分。在此我们报告,纳摩尔浓度的可溶性配体形式可完全消除这种排斥活性。用EphA3的可溶性胞外结构域也得到了类似结果,EphA3是Ephrin-A2和Ephrin-A5的受体,但用EphB3的相应结构域则未得到类似结果,EphB3是跨膜类Eph配体的受体。这些实验表明,条纹试验中所见的排斥性轴突导向活性是由Ephrin-A配体介导的。