Yan Ying-Gang, Zhang Jie, Xu Shu-Jun, Luo Jian-Hong, Qiu Shuang, Wang Wei
Neurosci Bull. 2014 Aug;30(4):655-66. doi: 10.1007/s12264-014-1450-8.
N-methyl-D-aspartate receptors (NMDARs) containing different GluN2 subunits play distinct roles in synaptic plasticity. Such differences may not only be determined by the channel properties, but also by differential surface distribution and synaptic localization.In the present study, using a Cy3-conjugated Fab fragment of the GFP antibody to label surface-located GluN2 subunits tagged with GFP at the N-terminus,we observed the membrane distribution patterns of GluN2A- or GluN2B-containing NMDARs in cultured rat hippocampal neurons. We found that surface NMDARs containing GluN2A, but not those containing GluN2B,were inclined to cluster at DIV7. Swapping the carboxyl termini of the GluN2 subunits completely reversed these distribution patterns. In addition, surface NMDARs containing GluN2A were preferentially associated with PSD-95. Taken together, the results of our study suggest that the clustering distribution of GluN2A containing NMDARs is determined by the GluN2AC-terminus, and its interaction with PSD-95 plays animportant role in this process.
含有不同GluN2亚基的N-甲基-D-天冬氨酸受体(NMDARs)在突触可塑性中发挥着不同的作用。这种差异可能不仅由通道特性决定,还由不同的表面分布和突触定位决定。在本研究中,我们使用GFP抗体的Cy3偶联Fab片段标记在N端带有GFP标记的位于表面的GluN2亚基,观察了培养的大鼠海马神经元中含GluN2A或GluN2B的NMDARs的膜分布模式。我们发现,含有GluN2A的表面NMDARs在第7天倾向于聚集,而含有GluN2B的则不然。交换GluN2亚基的羧基末端完全逆转了这些分布模式。此外,含有GluN2A的表面NMDARs优先与PSD-95结合。综上所述,我们的研究结果表明,含GluN2A的NMDARs成簇分布由GluN2A的C末端决定,其与PSD-95的相互作用在此过程中起重要作用。