van den Pol A N
Section of Neurosurgery, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
J Comp Neurol. 1995 Aug 21;359(2):253-71. doi: 10.1002/cne.903590206.
The mitral cell of the olfactory bulb is the primary relay neuron that transmits information from the olfactory receptors to the rest of the brain. This excitatory neuron releases glutamate from presynaptic dendrites and axon terminals. All rat mitral cells studied showed strong, selective, and widespread metabotropic glutamate receptor mGluR1 alpha immunoreactivity on the presynaptic membrane of dendrites, often at the synaptic vesicle release site, when examined with light and electron microscopy. The finding of glutamate receptors on mitral cell secondary dendrites supports the conclusion that not all dendritic membrane with glutamate receptors necessarily have gray type I asymmetrical synaptic specializations. In contrast, the metabotropic glutamate receptor mGluR5 was not found in mitral cells but was expressed by granule cells and astrocytes around mitral dendrites. Both mGluR1 alpha and mGluR5 were expressed early in development, with strong immunostaining present by postnatal day 1. MGluR1 alpha staining at birth mirrored the adult staining pattern. MGluR5 staining at birth showed different patterns of immunostaining than that found in the adult, particularly in the external plexiform layer. In vitro olfactory bulb neurons and their dendrites from embryonic day (E) 18 olfactory bulbs responded to t-ACPD and quisqualate, selective and nonselective metabotropic glutamate receptor agonists, and to several ionotropic glutamate agonists with increases in intracellular Ca2+ as studied with fura-2 digital imaging. These data indicate that the receptors were functionally active at an early stage of development. Application of the glutamate receptor blockers d-2-amino-5-phosphonovalerate (AP5) and 6-cyano-7-nitroquinoxaline (CNQX) to E17 olfactory bulb neurons after only 4 days in vitro resulted in a dramatic decrease in Ca2+ levels in 70% of 128 cells tested, suggesting that embryonic neurons after a short time in vitro can actively secrete glutamate. The presence of glutamate receptors on the long mitral cell dendrite suggests that it would be able to respond to release of its own excitatory transmitter, probably at an early stage of development. In the probable absence of other excitatory input to the secondary mitral dendrites, it would be the only excitatory "input." This autoexcitatory response would be modulated by release of GABA from olfactory interneurons occurring milliseconds after glutamate release induced by olfactory nerve activation. This novel type of neuronal microcircuitry would potentially amplify signal transmission and current spread along the long mitral dendrites and could play an important role in lateral inhibition of olfactory neurons.
嗅球的二尖瓣细胞是主要的中继神经元,它将嗅觉受体的信息传递到大脑的其他部分。这种兴奋性神经元从突触前树突和轴突末端释放谷氨酸。用光镜和电镜检查时,所有研究的大鼠二尖瓣细胞在树突的突触前膜上都显示出强烈、选择性和广泛的代谢型谷氨酸受体mGluR1α免疫反应性,通常在突触小泡释放部位。在二尖瓣细胞二级树突上发现谷氨酸受体支持了这样的结论,即并非所有带有谷氨酸受体的树突膜都必然具有I型灰色不对称突触特化。相反,在二尖瓣细胞中未发现代谢型谷氨酸受体mGluR5,但在二尖瓣树突周围的颗粒细胞和星形胶质细胞中表达。mGluR1α和mGluR5在发育早期就有表达,出生后第1天就有强烈的免疫染色。出生时mGluR1α染色反映了成年染色模式。出生时mGluR5染色显示出与成年时不同的免疫染色模式,特别是在外部丛状层。用fura-2数字成像研究发现,来自胚胎第18天(E18)嗅球的体外培养的嗅球神经元及其树突对t-ACPD和quisqualate(选择性和非选择性代谢型谷氨酸受体激动剂)以及几种离子型谷氨酸激动剂有反应,细胞内Ca2+增加。这些数据表明这些受体在发育早期就具有功能活性。在体外培养仅4天后,将谷氨酸受体阻滞剂d-2-氨基-5-磷酸戊酸(AP5)和6-氰基-7-硝基喹喔啉(CNQX)应用于E17嗅球神经元,导致所测试的128个细胞中有70%的细胞Ca2+水平显著下降,这表明体外培养短时间后的胚胎神经元能够主动分泌谷氨酸。二尖瓣细胞长树突上存在谷氨酸受体表明它可能在发育早期就能对自身兴奋性递质的释放做出反应。在二级二尖瓣树突可能没有其他兴奋性输入的情况下,它将是唯一的兴奋性“输入”。这种自激反应将受到嗅觉中间神经元释放的GABA的调节,GABA在嗅觉神经激活诱导谷氨酸释放后几毫秒内释放。这种新型的神经元微电路可能会放大信号传递和电流沿二尖瓣长树突的传播,并可能在嗅觉神经元的侧向抑制中发挥重要作用。