Division of Neurobiology, Department Biology II, Ludwig-Maximilians-Universität Munich, Germany.
J Neurophysiol. 2012 Feb;107(4):1186-98. doi: 10.1152/jn.00586.2011. Epub 2011 Nov 30.
Neurons of the medial superior olive (MSO) code for the azimuthal location of low-frequency sound sources via a binaural coincidence detection system operating on microsecond time scales. These neurons are morphologically simple and stereotyped, and anatomical studies have indicated a functional segregation of excitatory and inhibitory inputs between cellular compartments. It is thought that this morphological arrangement holds important implications for the computational task of these cells. To date, however, there has been no functional investigation into synaptic input sites or functional receptor distributions on mature neurons of the MSO. Here, functional neurotransmitter receptor maps for amino-3-hydroxyl-5-methyl-4-isoxazole propionate (AMPA), N-methyl-D-aspartate (NMDA), glycine (Gly), and ionotropic γ-aminobutyric acid (GABA(A)) receptors (Rs) were compared and complemented by their corresponding synaptic input map. We find in MSO neurons from postnatal day 20-35 gerbils that AMPARs and their excitatory inputs target the soma and dendrites. Functional GlyRs and their inhibitory inputs are predominantly refined to the somata, although a pool of functional GlyRs is present extrasynaptically on MSO dendrites. GABA(A)R responses are present throughout the cell but lack direct synaptic contact indicating an involvement in volume transmission. NMDARs are present both synaptically and extrasynaptically with an overall distribution similar to GlyRs. Interestingly, even at physiological temperatures these functional NMDARs can be potentiated by synaptically released Gly. The functional receptor and synaptic input maps produced here led to the identification of a cross talk between transmitter systems and raises the possibility that extrasynaptic receptors could be modulating leak conductances as a homeostatic mechanism.
中脑上橄榄复合体(MSO)的神经元通过在微秒时间尺度上运行的双耳 coincidence 检测系统对低频声源的方位进行编码。这些神经元形态简单且刻板,解剖学研究表明兴奋性和抑制性输入在细胞区室之间存在功能分离。人们认为这种形态排列对这些细胞的计算任务具有重要意义。然而,迄今为止,对于 MSO 成熟神经元的突触输入位点或功能性受体分布,尚未进行功能研究。在这里,我们比较了代谢型谷氨酸受体(AMPA)、N-甲基-D-天冬氨酸受体(NMDA)、甘氨酸受体(Gly)和离子型γ-氨基丁酸 A 型受体(GABA(A)Rs)的功能性神经递质受体图谱,并通过相应的突触输入图谱进行了补充。我们发现,在出生后 20-35 天的沙鼠 MSO 神经元中,AMPA 受体及其兴奋性输入靶向胞体和树突。功能性 GlyRs 及其抑制性输入主要集中在胞体上,尽管 MSO 树突上存在一定数量的功能性 GlyRs 位于突触外。GABA(A)R 反应存在于整个细胞中,但缺乏直接的突触接触,表明其参与了容积传递。NMDA 受体存在于突触内和突触外,其整体分布与 GlyRs 相似。有趣的是,即使在生理温度下,突触释放的 Gly 也可以增强这些功能性 NMDA 受体。这里产生的功能性受体和突触输入图谱导致了递质系统之间的串扰,并提出了突触外受体可能作为一种稳态机制调节漏电流的可能性。