Greengard P, Valtorta F, Czernik A J, Benfenati F
Laboratory of Molecular and Cellular Neuroscience, Rockefeller University, New York, NY 10021.
Science. 1993 Feb 5;259(5096):780-5. doi: 10.1126/science.8430330.
Complex brain functions, such as learning and memory, are believed to involve changes in the efficiency of communication between nerve cells. Therefore, the elucidation of the molecular mechanisms that regulate synaptic transmission, the process of intercellular communication, is an essential step toward understanding nervous system function. Several proteins associated with synaptic vesicles, the organelles that store neurotransmitters, are targets for protein phosphorylation and dephosphorylation. One of these phosphoproteins, synapsin I, by means of changes in its state of phosphorylation, appears to control the fraction of synaptic vesicles available for release and thereby to regulate the efficiency of neurotransmitter release. This article describes current understanding of the mechanism by which synapsin I modulates communication between nerve cells and reviews the properties and putative functions of other phosphoproteins associated with synaptic vesicles.
诸如学习和记忆等复杂的大脑功能被认为与神经细胞之间通讯效率的变化有关。因此,阐明调节突触传递(细胞间通讯过程)的分子机制是理解神经系统功能的关键一步。几种与突触小泡(储存神经递质的细胞器)相关的蛋白质是蛋白质磷酸化和去磷酸化的靶点。这些磷蛋白之一,突触素I,通过其磷酸化状态的变化,似乎可以控制可供释放的突触小泡的比例,从而调节神经递质释放的效率。本文描述了目前对突触素I调节神经细胞间通讯机制的理解,并综述了与突触小泡相关的其他磷蛋白的特性和假定功能。