Ryan T A, Smith S J
Department of Molecular and Cellular Physiology, Stanford University, California 94305, USA.
Neuron. 1995 May;14(5):983-9. doi: 10.1016/0896-6273(95)90336-4.
Using the fluorescent membrane label FM 1-43, we have measured the release, reuptake, and repriming of synaptic vesicles in response to action potential stimulation of cultured hippocampal neurons. We find that approximately 90% of a recycling vesicle pool is released during 60 s of 10 Hz action potential firing, and that a single action potential releases approximately 0.5% of that pool. Our data also indicate that endocytic reuptake of vesicle membrane externalized by 10 Hz action potentials lags exocytosis, with a half-time on the order of 20 s, and that the minimum time for repriming of an endocytosed vesicle is on the order of 15 s. Finally, we find that once vesicles have undergone this repriming period, they become functionally mixed in the vesicle pool within a few minutes; the probability of release for recently recycled vesicles is indistinguishable from that of vesicles that have resided within the bouton for much longer periods.
使用荧光膜标记物FM 1-43,我们测量了培养的海马神经元在动作电位刺激下突触小泡的释放、再摄取和再引发过程。我们发现,在10 Hz动作电位发放60秒期间,约90%的循环小泡池被释放,单个动作电位释放该池的约0.5%。我们的数据还表明,10 Hz动作电位使小泡膜外化后的内吞再摄取滞后于胞吐作用,半衰期约为20秒,内吞小泡再引发的最短时间约为15秒。最后,我们发现,一旦小泡经历了这个再引发期,它们在几分钟内就会在小泡池中功能混合;最近循环的小泡的释放概率与在突触小体中停留时间长得多的小泡的释放概率没有区别。