Johnson R R, Jiang X, Burkhalter A
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis Missouri 63110, USA.
J Comp Neurol. 1996 May 6;368(3):335-55. doi: 10.1002/(SICI)1096-9861(19960506)368:3<335::AID-CNE2>3.0.CO;2-6.
Changes in N-methyl-D-aspartate (NMDA) receptor expression may represent a molecular substrate for differences in synaptic plasticity between early postnatal and adult brains (Fox and Zahs [1994] Curr. Opinion Neurobiol. 4:112-119). We have, therefore, examined the regional and laminar distribution of NR1, the essential subunit of the NMDA receptor, in two regions in which synaptic plasticity has been most thoroughly studied: primary visual cortex and hippocampus. To study NR1 expression at the light and electron microscopic levels we have used a new antiserum (NR1-C1; Sheng et al. [1994] Nature 368:144-147) directed against a differentially spliced C-terminal exon ("C1"). The most striking result was that the pattern of NR1-C1 labeling in the adult was more restricted than that of previously published NR1-specific antibodies. Specifically, NR1-C1 did not label cells in the CA3, dentate gyrus or subicular regions of the hippocampus or in layer 4 of the visual cortex. Quantitative ultrastructural analysis revealed that these differences were paralleled by differential expression of NR1-C1 at synapses. In sharp contrast to the pattern in the adult, NR1-C1 immunoreactivity was distributed more widely in the developing brain. At postnatal day 11, NR1-C1 splice variants were expressed in all layers of the visual cortex and in all regions of the hippocampus. The transient expression of NR1-C1 splice variants in layer 4 of visual cortex suggests that NR1-C1 may play a role in determining the critical period for binocular plasticity. Continued expression of NR1-C1 in upper and lower layers of the adult cortex and in CA1 of the hippocampus may provide a substrate for plasticity in corticocortical connections and Schaffer collateral synapses beyond the critical period. In addition to abundant postsynaptic staining, NR1-C1 immunoreactivity was found in a large number of axon terminals in the dorsal subiculum, but in very few terminals in visual cortex. This strongly suggests that presynaptic NMDA receptors play a major role in neuronal processing of hippocampal output through the subiculum, but play a relatively minor role in visual processing.
N-甲基-D-天冬氨酸(NMDA)受体表达的变化可能代表了出生后早期大脑与成年大脑之间突触可塑性差异的分子基础(Fox和Zahs [1994]《当代神经生物学观点》4:112 - 119)。因此,我们研究了NMDA受体的必需亚基NR1在两个突触可塑性研究最为深入的区域:初级视皮层和海马体中的区域及层状分布。为了在光镜和电镜水平研究NR1的表达,我们使用了一种新的抗血清(NR1-C1;Sheng等人[1994]《自然》368:144 - 147),其针对一个差异剪接的C末端外显子(“C1”)。最显著的结果是,成年动物中NR1-C1标记的模式比先前发表的NR1特异性抗体的模式更具局限性。具体而言,NR1-C1在海马体的CA3、齿状回或下托区域以及视皮层第4层中不标记细胞。定量超微结构分析表明,这些差异与NR1-C1在突触处的差异表达相对应。与成年动物的模式形成鲜明对比的是,NR1-C1免疫反应性在发育中的大脑中分布更为广泛。在出生后第11天,NR1-C1剪接变体在视皮层的所有层以及海马体的所有区域均有表达。视皮层第4层中NR1-C1剪接变体的短暂表达表明,NR1-C1可能在确定双眼可塑性的关键期方面发挥作用。成年皮层上层和下层以及海马体CA1中NR1-C1的持续表达可能为关键期之后的皮质皮质连接和谢弗侧支突触可塑性提供基础。除了丰富的突触后染色外,在背侧下托的大量轴突终末中发现了NR1-C1免疫反应性,但在视皮层的终末中很少见。这强烈表明,突触前NMDA受体在通过下托对海马体输出的神经元处理中起主要作用,但在视觉处理中起相对较小的作用。