Wu L G, Betz W J
Department of Physiology, University of Colorado Medical School, Denver 80262, USA.
Neuron. 1996 Oct;17(4):769-79. doi: 10.1016/s0896-6273(00)80208-1.
We used FM1-43 imaging and intracellular recordings of synaptic potentials to measure the time course of endocytosis in frog motor nerve terminals following tetanic nerve stimulation, and we used fura-2 imaging of intraterminal Ca2+ concentration to compare endocytic rate and [Ca2+]i. Following a 30 Hz tetanus, endocytosis declined exponentially with a time constant that depended on the duration of stimulation. The level of [Ca2+]i rose from a resting value of about 100 nM to more than 500 nM during 30 Hz stimulation, and rapidly declined to 200-250 nM after stimulation. [Ca2+]i returned to resting level with a time course that, like endocytosis, depended on the duration of tetanic stimulation. However, the rate of [Ca2+]i recovery was much slower than the rate of endocytosis, leading to the conclusion that endocytic rate is not determined solely by the instantaneous level of [Ca2+]i.
我们使用FM1-43成像和突触电位的细胞内记录来测量强直神经刺激后青蛙运动神经末梢内吞作用的时间进程,并且我们使用fura-2成像来测量末梢内Ca2+浓度,以比较内吞速率和[Ca2+]i。在30Hz强直刺激后,内吞作用呈指数下降,其时间常数取决于刺激的持续时间。在30Hz刺激期间,[Ca2+]i水平从约100nM的静息值升至超过500nM,并在刺激后迅速降至200-250nM。[Ca2+]i恢复到静息水平的时间进程,与内吞作用一样,取决于强直刺激的持续时间。然而,[Ca2+]i恢复的速率比内吞作用的速率慢得多,从而得出结论,内吞速率并非仅由[Ca2+]i的瞬时水平决定。