von Gersdorff H, Sakaba T, Berglund K, Tachibana M
Department of Membrane Biophysics, Max Planck Institute for Biophysical Chemistry, Am Fassberg, Göttingen, Federal Republic of Germany.
Neuron. 1998 Nov;21(5):1177-88. doi: 10.1016/s0896-6273(00)80634-0.
Exocytosis-mediated glutamate release from ribbon-type synaptic terminals of retinal bipolar cells was studied using AMPA receptors and simultaneous membrane capacitance measurements. Release onset (delay <0.8 ms) and offset were closely tied to Ca2+ channel opening and closing. Asynchronous release was not copious and we estimate that there are approximately 5 Ca2+ channels per docked synaptic vesicle. Depending on Ca2+ current amplitude, release occurred in a single fast bout or in two successive bouts with fast and slow onset kinetics. The second, slower bout may reflect a mobilization rate of reserve vesicles toward fusion sites that is accelerated by increasing Ca2+ influx. Bipolar cell synaptic ribbons thus are remarkably versatile signal transducers, capable of transmitting rapidly changing sensory input, as well as sustained stimuli, due to their large pool of releasable vesicles.
利用AMPA受体和同步膜电容测量技术,研究了视网膜双极细胞带状突触终末通过胞吐作用释放谷氨酸的过程。释放的起始(延迟<0.8毫秒)和终止与Ca2+通道的开放和关闭密切相关。异步释放并不大量,我们估计每个停靠的突触小泡约有5个Ca2+通道。根据Ca2+电流幅度,释放以单次快速发作或两次连续发作的形式出现,发作动力学有快有慢。第二次较慢的发作可能反映了储备小泡向融合位点的动员速率,这种动员速率会因Ca2+内流增加而加快。因此,双极细胞突触带是非常通用的信号转导器,由于其大量可释放的小泡,能够传递快速变化的感觉输入以及持续的刺激。