Micheva Kristina D, Buchanan JoAnn, Holz Ronald W, Smith Stephen J
Department of Molecular and Cellular Physiology, Stanford University, Stanford, California 94305, USA.
Nat Neurosci. 2003 Sep;6(9):925-32. doi: 10.1038/nn1114.
Sustained release of neurotransmitter depends upon the recycling of synaptic vesicles. Until now, it has been assumed that vesicle recycling is regulated by signals from the presynaptic bouton alone, but results from rat hippocampal neurons reported here indicate that this need not be the case. Fluorescence imaging and pharmacological analysis show that a nitric oxide (NO) signal generated postsynaptically can regulate endocytosis and at least one later step in synaptic vesicle recycling. The proposed retrograde pathway involves an NMDA receptor (NMDAR)-dependent postsynaptic production of NO, diffusion of NO to a presynaptic site, and a cGMP-dependent increase in presynaptic phosphatidylinositol 4,5-biphosphate (PIP2). These results indicate that the regulation of synaptic vesicle recycling may integrate a much broader range of neural activity signals than previously recognized, including postsynaptic depolarization and the activation of NMDARs at both immediate and nearby postsynaptic active zones.
神经递质的持续释放依赖于突触小泡的循环利用。到目前为止,人们一直认为小泡循环仅由来自突触前终扣的信号调节,但此处报道的大鼠海马神经元实验结果表明并非一定如此。荧光成像和药理学分析显示,突触后产生的一氧化氮(NO)信号可调节内吞作用以及突触小泡循环利用过程中的至少一个后续步骤。所提出的逆行途径涉及NMDA受体(NMDAR)依赖的突触后NO生成、NO扩散至突触前位点以及突触前磷脂酰肌醇4,5-二磷酸(PIP2)的cGMP依赖性增加。这些结果表明,突触小泡循环利用的调节可能整合了比之前认识到的范围更广的神经活动信号,包括突触后去极化以及紧邻和附近突触后活动区的NMDAR激活。