Department of Pharmacology, UC Davis School of Medicine, 3503 Genome & Biomedical Sciences Facility, Davis, CA 95616, USA.
J Physiol. 2012 Jan 1;590(1):33-8. doi: 10.1113/jphysiol.2011.213884. Epub 2011 Aug 30.
During development of the central nervous system (CNS), precise synaptic connections between pre- and postsynaptic neurons are formed that ultimately give rise to higher order cognitive skills such as learning and memory. Previously, my group identified a novel type II transmembrane protein, synapse differentiation induced gene 1 (SynDIG1), that regulates synaptic AMPA receptor content in dissociated rat hippocampal neurons. The magnitude of this effect matches that of the prototypical scaffold postsynaptic density protein of 95 kDa (PSD-95) identifying SynDIG1 as a previously unknown central regulator of excitatory synaptic strength. SynDIG1-mediated regulation of synaptic AMPA receptor targeting shares characteristics related to two distinct classes of transmembrane synaptic proteins: (1) ion channel auxiliary factors such as transmembrane AMPA receptor regulatory proteins (TARPs) important for AMPA receptor surface expression and channel gating properties; and (2) trans-synaptic organizing molecules such as leucine rich repeat transmembrane protein 2 (LRRTM2) that influence synapse maturation by recruitment of AMPA receptors to nascent synapses. An interesting aspect of SynDIG1 is that its distribution at excitatory synapses is regulated by activity, suggesting that SynDIG1 might also play a role in synaptic plasticity.
在中枢神经系统 (CNS) 的发育过程中,前突触神经元和后突触神经元之间形成了精确的突触连接,最终产生了更高阶的认知技能,如学习和记忆。此前,我的研究小组发现了一种新型的 II 型跨膜蛋白,突触分化诱导基因 1 (SynDIG1),它调节分离的大鼠海马神经元中突触 AMPA 受体的含量。这种效应的大小与典型的突触后密度蛋白 95kDa (PSD-95) 的效应相当,表明 SynDIG1 是一种以前未知的中枢兴奋性突触强度调节因子。SynDIG1 介导的突触 AMPA 受体靶向调节与两类不同的跨膜突触蛋白具有共同特征:(1) 离子通道辅助因子,如对于 AMPA 受体表面表达和通道门控特性很重要的跨膜 AMPA 受体调节蛋白 (TARPs);(2) 跨突触组织分子,如富含亮氨酸的重复跨膜蛋白 2 (LRRTM2),通过将 AMPA 受体募集到新生突触来影响突触成熟。SynDIG1 的一个有趣方面是,它在兴奋性突触中的分布受活动调节,这表明 SynDIG1 可能在突触可塑性中也发挥作用。