Lenzi David, Crum John, Ellisman Mark H, Roberts William M
Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA.
Neuron. 2002 Nov 14;36(4):649-59. doi: 10.1016/s0896-6273(02)01025-5.
We used electron tomography of frog saccular hair cells to reconstruct presynaptic ultrastructure at synapses specialized for sustained transmitter release. Synaptic vesicles at inhibited synapses were abundant in the cytoplasm and covered the synaptic body at high density. Continuous maximal stimulation depleted 73% of the vesicles within 800 nm of the synapse, with a concomitant increase in surface area of intracellular cisterns and plasmalemmal infoldings. Docked vesicles were depleted 60%-80% regardless of their distance from the active zone. Vesicles on the synaptic body were depleted primarily in the hemisphere facing the plasmalemma, creating a gradient of vesicles on its surface. We conclude that formation of new synaptic vesicles from cisterns is rate limiting in the vesicle cycle.
我们利用青蛙球囊毛细胞的电子断层扫描技术,重建了专门用于持续递质释放的突触处的突触前超微结构。抑制性突触处的突触小泡在细胞质中丰富,高密度覆盖突触体。连续最大刺激使突触800纳米范围内73%的小泡耗尽,同时细胞内池和质膜内褶的表面积增加。无论与活性区的距离如何,停靠的小泡减少60%-80%。突触体上的小泡主要在面向质膜的半球耗尽,在其表面形成小泡梯度。我们得出结论,从池形成新的突触小泡在小泡循环中是限速步骤。