Levy Robert B, Aoki Chiye
New York University Center for Neural Science, New York, New York 10003, USA.
J Neurosci. 2002 Jun 15;22(12):5001-15. doi: 10.1523/JNEUROSCI.22-12-05001.2002.
NMDA receptor (NMDAR) activation requires concurrent membrane depolarization, and glutamatergic synapses lacking AMPA receptors (AMPARs) are often considered "silent" in the absence of another source of membrane depolarization. During the second postnatal week, NMDA currents can be enhanced in rat auditory cortex through activation of the alpha7 nicotinic acetylcholine receptor (alpha7nAChR). Electrophysiological results support a mainly presynaptic role for alpha7nAChR at these synapses. However, immunocytochemical evidence that alpha7nAChR is prevalent at postsynaptic sites of glutamatergic synapses in hippocampus and neocortex, along with emerging electrophysiological evidence for postsynaptic nicotinic currents in neocortex and hippocampus, has prompted speculation that alpha7nAChR allows for activation of NMDAR postsynaptically at synapses lacking AMPAR. Here we used dual immunolabeling and electron microscopy to examine the distribution of alpha7nAChR relative to AMPAR (GluR1, GluR2, and GluR3 subunits combined) at excitatory synapses in somatosensory cortex of adult and 1-week-old rats. alpha7nAChR occurred discretely over most of the thick postsynaptic densities in all cortical layers of both age groups. AMPAR immunoreactivity was also detectable at most synapses; its distribution was independent of that of alpha7nAChR. In both age groups, approximately one-quarter of asymmetrical synapses were alpha7nAChR positive and AMPAR negative. The variability of postsynaptic alpha7nAChR labeling density was greater at postnatal day (PD) 7 than in adulthood, and PD 7 neuropil contained a subset of small AMPA receptor-negative synapses with a high density of alpha7nAChR immunoreactivity. These observations support the idea that acetylcholine receptors can aid in activating glutamatergic synapses and work together with AMPA receptors to mediate postsynaptic excitation throughout life.
N-甲基-D-天冬氨酸受体(NMDAR)的激活需要同时发生膜去极化,并且在缺乏另一种膜去极化来源的情况下,缺乏α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR)的谷氨酸能突触通常被认为是“沉默的”。在出生后第二周,通过激活α7烟碱型乙酰胆碱受体(α7nAChR),大鼠听觉皮层中的NMDA电流可以增强。电生理结果支持α7nAChR在这些突触中主要起突触前作用。然而,免疫细胞化学证据表明α7nAChR在海马体和新皮层的谷氨酸能突触的突触后位点普遍存在,以及新皮层和海马体中出现的突触后烟碱电流的电生理证据,促使人们推测α7nAChR允许在缺乏AMPAR的突触处突触后激活NMDAR。在这里,我们使用双重免疫标记和电子显微镜来检查成年和1周龄大鼠体感皮层兴奋性突触处α7nAChR相对于AMPAR(GluR1、GluR2和GluR3亚基组合)的分布。在两个年龄组的所有皮层层中,α7nAChR离散地出现在大多数厚突触后致密物上。在大多数突触处也可检测到AMPAR免疫反应性;其分布与α7nAChR的分布无关。在两个年龄组中,大约四分之一的不对称突触α7nAChR呈阳性而AMPAR呈阴性。出生后第7天(PD7)突触后α7nAChR标记密度的变异性比成年期更大,并且PD7神经毡包含一小部分小的AMPA受体阴性突触,其α7nAChR免疫反应性密度很高。这些观察结果支持这样一种观点,即乙酰胆碱受体可以帮助激活谷氨酸能突触,并与AMPA受体一起在整个生命过程中介导突触后兴奋。