Plunkett J A, Baccus S A, Bixby J L
Department of Molecular and Cellular Pharmacology, University of Miami School of Medicine, Miami, Florida 33136, USA.
J Neurosci. 1998 Aug 1;18(15):5832-8. doi: 10.1523/JNEUROSCI.18-15-05832.1998.
Differentiation of presynaptic nerve terminals involves changes in gene expression; these may be regulated by synaptic transmission and/or by contact with the target muscle. To gain insight into the control of presynaptic differentiation, we examined the regulation by target and synaptic activity of synaptic vesicle protein (SVP) genes in the chick ciliary ganglion (CG). In the CG, two SVP genes, synaptotagmin I (syt I) and synaptophysin II (syp II), are coordinately upregulated at the time of target contact. To test the hypothesis that this upregulation is induced by target contact, we examined mRNA levels of syt I and syp II in CGs from embryos in which one eye had been removed before axon outgrowth. As expected, target removal prevented the normal upregulation of syt I mRNA in the deprived ganglion. In contrast, and unexpectedly, syp II mRNA upregulation was not affected. The target dependence of syt I upregulation was not attributable to nerve-muscle transmission, because blockade of this transmission had no effect on SVP mRNA levels. Surprisingly, blockade of synapses onto CG neurons from the brain also did not affect syt I mRNA levels but increased levels of syp II mRNA. We conclude that contact with target induces upregulation of syt I mRNA, which is the case for spinal motor neurons. However, the normal upregulation of syp II mRNA is not controlled by the same signal(s). Instead, our results suggest that these two SVP genes are differentially regulated, both by target contact and by blockade of synaptic transmission.
突触前神经末梢的分化涉及基因表达的变化;这些变化可能受突触传递和/或与靶肌肉接触的调控。为深入了解突触前分化的控制机制,我们研究了鸡睫状神经节(CG)中突触囊泡蛋白(SVP)基因受靶标和突触活动的调控情况。在CG中,两个SVP基因,即突触结合蛋白I(syt I)和突触素II(syp II),在与靶标接触时会协同上调。为验证这种上调是由靶标接触诱导的这一假说,我们检测了在轴突生长前一只眼睛已被摘除的胚胎的CG中syt I和syp II的mRNA水平。正如预期的那样,靶标去除阻止了去神经节中syt I mRNA的正常上调。然而,出乎意料的是,syp II mRNA的上调并未受到影响。syt I上调对靶标的依赖性并非归因于神经 - 肌肉传递,因为阻断这种传递对SVP mRNA水平没有影响。令人惊讶的是,阻断来自大脑的CG神经元突触也不影响syt I mRNA水平,但会增加syp II mRNA水平。我们得出结论,与靶标接触会诱导syt I mRNA上调,脊髓运动神经元也是如此。然而,syp II mRNA的正常上调不受相同信号的控制。相反,我们的结果表明,这两个SVP基因在靶标接触和突触传递阻断方面受到不同的调控。