Cathala L, Misra C, Cull-Candy S
Department of Pharmacology, University College London, London WC1E 6BT, United Kingdom.
J Neurosci. 2000 Aug 15;20(16):5899-905. doi: 10.1523/JNEUROSCI.20-16-05899.2000.
During cerebellar development, granule cells display well characterized changes in the expression of NMDA receptor (NMDAR) NR2 subunits, switching from NR2B to NR2A and NR2C in mature cells. Although various studies, including experiments on mutant mice with one or more NR2 subunit types deleted, suggest that NR2A, NR2B, and NR2C subunits contribute to synaptic NMDARs, changes in the properties of the mossy fiber EPSC during development have not been fully evaluated. In particular, information on NMDAR EPSCs in mature animals is lacking. We have examined pharmacological and kinetic properties of NMDARs at mossy fiber-granule cell synapses from their formation to maturity [postnatal day 7 (P7)-P40 rats]. Significant changes were seen in the relative amplitudes of the non-NMDAR- and NMDAR-mediated components of the evoked EPSC and in the decay kinetics of the latter. The NMDA/non-NMDA ratio was similar at P7, P21, and P40, but showed a clear peak at P12. This change coincided with a speeding of the NMDAR EPSC decay, accompanied by a decrease in sensitivity to ifenprodil (selective NR2B-antagonist). By P21, sensitivity of the NMDAR EPSC to Mg(2+) was approximately threefold less than that at P12 (IC(50), 76 vs 28 microm), suggesting incorporation of the NR2C subunit. However, the predicted slowing of decay kinetics to a value more characteristic of NR2C deactivation, was not seen until P40. Our data are consistent with the known switch from NR2B to NR2A subunits during the first two postnatal weeks, but suggest a gradual incorporation of the NR2C subunit that modifies Mg(2+) sensitivity and only later influences EPSC kinetics.
在小脑发育过程中,颗粒细胞在N-甲基-D-天冬氨酸受体(NMDAR)NR2亚基的表达上呈现出特征明确的变化,从NR2B转变为成熟细胞中的NR2A和NR2C。尽管包括对缺失一种或多种NR2亚基类型的突变小鼠进行的实验在内的各种研究表明,NR2A、NR2B和NR2C亚基对突触NMDAR有贡献,但在发育过程中苔藓纤维兴奋性突触后电流(EPSC)特性的变化尚未得到充分评估。特别是,成熟动物中NMDAR EPSC的信息尚缺。我们研究了从出生后第7天(P7)到第40天(P40)大鼠的苔藓纤维-颗粒细胞突触处NMDAR的药理学和动力学特性,从其形成到成熟阶段。在诱发的EPSC的非NMDAR介导成分和NMDAR介导成分的相对幅度以及后者的衰减动力学方面均观察到显著变化。NMDA/非NMDA比值在P7、P21和P40时相似,但在P12时出现明显峰值。这种变化与NMDAR EPSC衰减加速同时出现,伴随着对ifenprodil(选择性NR2B拮抗剂)敏感性的降低。到P21时,NMDAR EPSC对Mg(2+)的敏感性比P12时降低了约三倍(半数抑制浓度,IC(50)分别为76和28微摩尔),表明NR2C亚基已掺入。然而,直到P40才观察到衰减动力学如预期那样减慢到更具NR2C失活特征的值。我们的数据与出生后前两周已知的从NR2B到NR2A亚基的转变一致,但表明NR2C亚基是逐渐掺入的,它改变了Mg(2+)敏感性,且仅在稍后才影响EPSC动力学。