Feng Jian, Chi Ping, Blanpied Thomas A, Xu Yimei, Magarinos Ana Maria, Ferreira Adriana, Takahashi Reisuke H, Kao Hung-Teh, McEwen Bruce S, Ryan Timothy A, Augustine George J, Greengard Paul
Laboratory of Molecular and Cellular Neuroscience and Laboratory of Endocrinology, The Rockefeller University, New York, New York 10021, USA.
J Neurosci. 2002 Jun 1;22(11):4372-80. doi: 10.1523/JNEUROSCI.22-11-04372.2002.
Synapsin III is the most recently identified member of the synapsin family, a group of synaptic vesicle proteins that play essential roles in neurotransmitter release and neurite outgrowth. Here, through the generation and analysis of synapsin III knock-out mice, we demonstrate that synapsin III regulates neurotransmitter release in a manner that is distinct from that of synapsin I or synapsin II. In mice lacking synapsin III, the size of the recycling pool of synaptic vesicles was increased, and synaptic depression was reduced. The number of vesicles that fuse per action potential was similar between synapsin III knock-out and wild-type mice, and there was no change in the quantal content of EPSCs; however, IPSCs were greatly reduced in synapsin III-deficient neurons. The density and distribution of synaptic vesicles in presynaptic terminals did not appear to be different in synapsin III knock-out mice in comparison to wild-type littermates. In addition to the changes in neurotransmitter release, we observed a specific delay in axon outgrowth in cultured hippocampal neurons from synapsin III knock-out mice. Our data indicate that synapsin III plays unique roles both in early axon outgrowth and in the regulation of synaptic vesicle trafficking.
突触结合蛋白III是突触结合蛋白家族中最近发现的成员,该家族是一组在神经递质释放和神经突生长中起关键作用的突触囊泡蛋白。在此,通过生成和分析突触结合蛋白III基因敲除小鼠,我们证明突触结合蛋白III以一种不同于突触结合蛋白I或突触结合蛋白II的方式调节神经递质释放。在缺乏突触结合蛋白III的小鼠中,突触囊泡循环池的大小增加,突触抑制减弱。突触结合蛋白III基因敲除小鼠和野生型小鼠每次动作电位融合的囊泡数量相似,兴奋性突触后电流(EPSCs)的量子含量没有变化;然而,在缺乏突触结合蛋白III的神经元中,抑制性突触后电流(IPSCs)大大减少。与野生型同窝小鼠相比,突触结合蛋白III基因敲除小鼠突触前终末中突触囊泡的密度和分布似乎没有差异。除了神经递质释放的变化外,我们还观察到来自突触结合蛋白III基因敲除小鼠的培养海马神经元轴突生长存在特定延迟。我们的数据表明,突触结合蛋白III在早期轴突生长和突触囊泡运输调节中都发挥着独特作用。