Miskevich Frank, Lu Wei, Lin Shuh-Yow, Constantine-Paton Martha
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139-4307, USA.
J Neurosci. 2002 Jan 1;22(1):226-38. doi: 10.1523/JNEUROSCI.22-01-00226.2002.
Recently, NMDA receptors (NMDARs) have been implicated in a cell contact-dependent suppression of sprouting in cultured Xenopus tectal neurons during an early period when neither AMPA/kainate (KA) receptors nor action potentials play a prominent role in cell-cell communication. We asked how the NMDA receptors function in the absence of the depolarizing effect of AMPA/KA receptor activity. We show that type II metabotropic glutamate receptors (mGluRs) can operate synergistically with NMDA receptors in the absence of AMPA/KA receptor function to suppress an early neurite sprouting response of the tectal neurons. Calcium imaging with fluo-3 AM and morphological analyses after exposure to glutamate receptor antagonists show that a combination of AMPA/KA receptor and type II mGluR blockers mimics the decrease in intracellular free calcium in response to glutamate and the structural effects produced by NMDA receptor antagonists in these cultures. Patch-clamp analyses confirmed a decrease in NMDA receptor-mediated currents with type II mGluR blockade, and 8-bromo cAMP application produced a decrease in NMDA receptor-mediated calcium influx. These data suggest that type II mGluRs potentiate NMDA receptor function by decreasing cAMP levels in tectal neurons. We also show that NMDARs exhibit low magnesium sensitivity in tectal neurons during the first few days in culture. Thus both metabotropic and ionotropic glutamate receptors can play a role in the contact-mediated suppression of ongoing sprouting at early neuron-neuron contacts before action potential activity.
最近,N-甲基-D-天冬氨酸受体(NMDARs)被认为在非洲爪蟾顶盖神经元培养过程中的早期,在一种细胞接触依赖性的轴突发芽抑制中发挥作用,此时α-氨基-3-羟基-5-甲基-4-异恶唑丙酸/海人藻酸(AMPA/KA)受体和动作电位在细胞间通讯中均未发挥显著作用。我们研究了在没有AMPA/KA受体活性的去极化作用时,NMDARs是如何发挥功能的。我们发现,在没有AMPA/KA受体功能的情况下,II型代谢型谷氨酸受体(mGluRs)可以与NMDARs协同作用,以抑制顶盖神经元早期的神经突发芽反应。用fluo-3 AM进行钙成像以及在暴露于谷氨酸受体拮抗剂后的形态学分析表明,AMPA/KA受体和II型mGluR阻滞剂的组合模拟了对谷氨酸的反应中细胞内游离钙的减少以及这些培养物中NMDAR拮抗剂产生的结构效应。膜片钳分析证实,II型mGluR阻断后NMDAR介导的电流减少,应用8-溴环磷酸腺苷(8-bromo cAMP)使NMDAR介导的钙内流减少。这些数据表明,II型mGluRs通过降低顶盖神经元中的环磷酸腺苷(cAMP)水平来增强NMDAR功能。我们还发现,在培养的头几天,顶盖神经元中的NMDARs对镁的敏感性较低。因此,在动作电位活动之前,代谢型和离子型谷氨酸受体都可以在早期神经元-神经元接触时接触介导的正在进行的轴突发芽抑制中发挥作用。