Lin R C, Scheller R H
Howard Hughes Medical Institute, Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, California 94305-5428, USA.
Annu Rev Cell Dev Biol. 2000;16:19-49. doi: 10.1146/annurev.cellbio.16.1.19.
Chemical synaptic transmission serves as the main form of cell to cell communication in the nervous system. Neurotransmitter release occurs through the process of regulated exocytosis, in which a synaptic vesicle releases its contents in response to an increase in calcium. The use of genetic, biochemical, structural, and functional studies has led to the identification of factors important in the synaptic vesicle life cycle. Here we focus on the prominent role of SNARE (soluble NSF attachment protein receptor) proteins during membrane fusion and the regulation of SNARE function by Rab3a, nSec1, and NSF. Many of the proteins important for transmitter release have homologs involved in intracellular vesicle transport, and all forms of vesicle trafficking share common basic principles. Finally, modifications to the synaptic exocytosis pathway are very likely to underlie certain forms of synaptic plasticity and therefore contribute to learning and memory.
化学突触传递是神经系统中细胞间通讯的主要形式。神经递质的释放通过调节性胞吐作用进行,在这个过程中,突触小泡会响应钙离子浓度的增加而释放其内容物。通过遗传、生化、结构和功能研究,已鉴定出在突触小泡生命周期中起重要作用的因子。在这里,我们重点关注SNARE(可溶性NSF附着蛋白受体)蛋白在膜融合过程中的突出作用,以及Rab3a、nSec1和NSF对SNARE功能的调节。许多对递质释放重要的蛋白质在细胞内囊泡运输中都有同源物,并且所有形式的囊泡运输都有共同的基本原理。最后,突触胞吐途径的修饰很可能是某些形式的突触可塑性的基础,因此有助于学习和记忆。