Department of Pharmacology and Psychiatry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-8548, USA.
Cold Spring Harb Perspect Biol. 2012 Feb 1;4(2):a005595. doi: 10.1101/cshperspect.a005595.
The regulated exocytosis that mediates chemical signaling at synapses requires mechanisms to coordinate the immediate response to stimulation with the recycling needed to sustain release. Two general classes of transporter contribute to release, one located on synaptic vesicles that loads them with transmitter, and a second at the plasma membrane that both terminates signaling and serves to recycle transmitter for subsequent rounds of release. Originally identified as the target of psychoactive drugs, these transport systems have important roles in transmitter release, but we are only beginning to understand their contribution to synaptic transmission, plasticity, behavior, and disease. Recent work has started to provide a structural basis for their activity, to characterize their trafficking and potential for regulation. The results indicate that far from the passive target of psychoactive drugs, neurotransmitter transporters undergo regulation that contributes to synaptic plasticity.
调节胞吐作用介导了突触处的化学信号传递,需要协调机制来将对刺激的即时反应与维持释放所需的再循环结合起来。有两类一般的转运蛋白有助于释放,一种位于突触小泡上,将递质装载到小泡中,另一种位于质膜上,既能终止信号传递,又能为随后的释放循环回收递质。这些转运系统最初被确定为精神活性药物的靶点,它们在递质释放中起着重要的作用,但我们才刚刚开始了解它们对突触传递、可塑性、行为和疾病的贡献。最近的工作已经开始为它们的活性提供结构基础,以描述它们的运输和潜在的调节。结果表明,神经递质转运体远非精神活性药物的被动靶点,它们会发生调节,从而促进突触可塑性。