Xu X M, Fisher D A, Zhou L, White F A, Ng S, Snider W D, Luo Y
Exelixis Pharmaceuticals, Inc., South San Francisco, California 94080, USA.
J Neurosci. 2000 Apr 1;20(7):2638-48. doi: 10.1523/JNEUROSCI.20-07-02638.2000.
Semaphorin 6A (Sema6A) (previously named Semaphorin VIa) is the originally described member of the vertebrate semaphorin class 6, a group of transmembrane semaphorins homologous to the insect semaphorin class 1. Although Sema-1a (previously named semaphorin I) has been implicated in axon guidance in insects, the function of Sema6A is currently unknown. We have expressed the extracellular domain of Sema6A in mammalian cells as either a monomeric or a dimeric fusion protein and tested for potential axon guidance effects on two populations of embryonic neurons in growth cone collapse and collagen matrix chemorepulsion assays. Sema6A was observed to induce growth cone collapse of sympathetic neurons with an EC50 of approximately 200 pM, although a 10-fold higher (EC50 of approximately 2 nM) concentration was necessary to induce growth cone collapse of dorsal root ganglion neurons. The activity of Sema6A is likely to depend on protein dimerization or oligomerization. Although Sema6A mRNA is expressed in complex patterns during embryonic development, it is strikingly absent from sympathetic ganglia. Sema6A is, however, expressed in areas avoided by sympathetic axons and in areas innervated by sympathetics, but before their arrival. Our results demonstrate that transmembrane semaphorins, like the secreted ones, can act as repulsive axon guidance cues. Our findings are consistent with a role for Sema6A in channeling sympathetic axons into the sympathetic chains and controlling the temporal sequence of sympathetic target innervation.
信号素6A(Sema6A)(先前称为信号素VIa)是脊椎动物信号素6类最初被描述的成员,这是一组与昆虫信号素1类同源的跨膜信号素。尽管信号素1a(先前称为信号素I)已被证明在昆虫轴突导向中起作用,但Sema6A的功能目前尚不清楚。我们在哺乳动物细胞中表达了Sema6A的胞外域,将其作为单体或二聚体融合蛋白,并在生长锥塌陷和胶原基质化学排斥试验中测试了其对两类胚胎神经元的潜在轴突导向作用。我们观察到Sema6A能诱导交感神经元的生长锥塌陷,其半数有效浓度(EC50)约为200皮摩尔,不过诱导背根神经节神经元的生长锥塌陷则需要高10倍(EC50约为2纳摩尔)的浓度。Sema6A的活性可能依赖于蛋白质二聚化或寡聚化。尽管Sema6A mRNA在胚胎发育过程中以复杂模式表达,但在交感神经节中却明显缺失。然而,Sema6A在交感轴突避开的区域以及由交感神经支配但在其到达之前的区域表达。我们的结果表明,跨膜信号素与分泌型信号素一样,可作为轴突导向的排斥性信号。我们的发现与Sema6A在引导交感轴突进入交感神经链以及控制交感神经靶标支配的时间顺序方面所起的作用一致。