Zisch A H, Pasquale E B
The Burnham Institute, 10901 N. Torrey Pines Road, La Jolla CA 92037, USA.
Cell Tissue Res. 1997 Nov;290(2):217-26. doi: 10.1007/s004410050926.
The Eph receptor tyrosine kinases are emerging as molecules that guide the migration of cells and growth cones during embryonic development. Based on their concentration in embryonic regions containing growing neuronal processes, the Eph receptors were suspected early on to have a role in regulating aspects of axon growth. The most distinctive role of the Eph receptors appears to be their ability to mediate cell-cell repulsion through the binding of a ligand on an adjacent cell surface. The repulsive interactions are presumably mediated by transient receptor activation at the boundaries of complementary regions of high ligand or receptor expression. In contrast, overlapping expression patterns may regulate cell adhesion and cytoskeletal organization with possible consequences on the overall growth and fasciculation of neuronal processes. A notable feature of Eph receptor signaling is that, upon receptor binding, responses may also be elicited in the ligand-expressing cells. A better understanding of Eph receptor function requires the elucidation of their signaling properties. Recent evidence suggests a functional interaction between the Eph receptor EphB2 and neural cell adhesion molecules of the L1 family, which have well-recognized roles in the formation of neuronal projections. Only a few cytoplasmic signaling molecules that bind to the activated Eph receptors have been identified. Several of these molecules are known to transduce signals regulating cytoskeletal organization and neurite outgrowth. It is currently unclear why there is a need for fourteen distinct Eph receptor genes, many of which appear to encode several variant forms with distinct functional properties, but it is tempting to speculate that such diversity is necessary to refine the spatial organization of embryonic structures.
Eph受体酪氨酸激酶正逐渐成为在胚胎发育过程中引导细胞和生长锥迁移的分子。基于它们在含有正在生长的神经突的胚胎区域中的浓度,Eph受体早在早期就被怀疑在调节轴突生长方面发挥作用。Eph受体最显著的作用似乎是它们能够通过与相邻细胞表面的配体结合来介导细胞间排斥。这种排斥性相互作用大概是由高表达配体或受体的互补区域边界处的瞬时受体激活介导的。相比之下,重叠的表达模式可能调节细胞黏附和细胞骨架组织,这可能对神经突的整体生长和束状化产生影响。Eph受体信号传导的一个显著特征是,在受体结合后,表达配体的细胞也可能引发反应。更好地理解Eph受体功能需要阐明它们的信号特性。最近的证据表明Eph受体EphB2与L1家族的神经细胞黏附分子之间存在功能相互作用,L1家族在神经元突起的形成中具有公认的作用。目前仅鉴定出少数几种与活化的Eph受体结合的细胞质信号分子。已知其中几种分子可转导调节细胞骨架组织和神经突生长的信号。目前尚不清楚为什么需要14个不同的Eph受体基因,其中许多似乎编码具有不同功能特性的几种变体形式,但很诱人推测这种多样性对于完善胚胎结构的空间组织是必要的。