Nestler E J, Greengard P
J Neurosci. 1982 Aug;2(8):1011-23. doi: 10.1523/JNEUROSCI.02-08-01011.1982.
The distribution and regulation of the state of phosphorylation of Protein I have been studied in the rabbit superior cervical sympathetic ganglion. The data indicate that the ganglion contains two pools of Protein I: a presynaptic pool that represents 60% of the total ganglion Protein I and a postsynaptic pool that represents 40% of the total ganglion Protein I. The state of phosphorylation of presynaptic Protein I, but not that of postsynaptic Protein I, is regulated by nerve impulse conduction, by dopamine, and by a high K+ concentration. Studies of the extracellular calcium requirements for Protein I phosphorylation, as well as peptide-mapping analyses of Protein I, suggest that the effects of nerve impulse conduction and of a high K+ concentration are mediated through the activation of calcium-dependent protein kinases and that the effect of dopamine is mediated through the activation of cyclic AMP-dependent protein kinase. The total amount of postsynaptic Protein I, but not that of presynaptic Protein I, is decreased by short periods of exposure to cycloheximide, a protein synthesis inhibitor. It is proposed that Protein I located in presynaptic nerve terminals plays a functional role in those terminals and that the Protein I located in cell bodies is newly synthesized and en route to nerve terminals.
已对兔颈上神经节中蛋白I的磷酸化状态分布及调节进行了研究。数据表明,该神经节含有两类蛋白I:一类是突触前池,占神经节总蛋白I的60%;另一类是突触后池,占神经节总蛋白I的40%。突触前蛋白I的磷酸化状态受神经冲动传导、多巴胺和高钾浓度的调节,而突触后蛋白I的磷酸化状态则不受这些因素影响。对蛋白I磷酸化所需细胞外钙的研究以及蛋白I的肽图分析表明,神经冲动传导和高钾浓度的作用是通过钙依赖性蛋白激酶的激活介导的,而多巴胺的作用是通过环磷酸腺苷依赖性蛋白激酶的激活介导的。短期暴露于蛋白质合成抑制剂环己酰亚胺会使突触后蛋白I的总量减少,但突触前蛋白I的总量不受影响。有人提出,位于突触前神经末梢的蛋白I在这些末梢中发挥功能作用,而位于细胞体中的蛋白I是新合成的,正在运往神经末梢的途中。