Issa N P, Hudspeth A J
Howard Hughes Medical Institute, Rockefeller University, New York, NY 10021-6399, USA.
Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9527-32. doi: 10.1073/pnas.93.18.9527.
Neurotransmitter is released when Ca2+ triggers the fusion of synaptic vesicles with the plasmalemma. To study factors that regulate Ca2+ concentration at the presynaptic active zones of hair cells, we used laser-scanning confocal microscopy with the fluorescent Ca2+ indicator fluo 3. The experimental results were compared with the predictions of a model of presynaptic Ca2+ concentration in which Ca2+ enters a cell through a point source, diffuses from the entry site, and binds to fixed or mobile Ca2+ buffers. The observed time course and magnitude of fluorescence changes under a variety of conditions were well fit when the model included mobile molecules as the only Ca2+ buffer. The results confirm the localized entry of Ca2+ underlying neurotransmitter release and suggest that Ca2+ is cleared from an active zone almost exclusively by mobile buffer.
当Ca2+触发突触小泡与质膜融合时,神经递质被释放。为了研究调节毛细胞突触前活性区Ca2+浓度的因素,我们使用了带有荧光Ca2+指示剂fluo 3的激光扫描共聚焦显微镜。将实验结果与突触前Ca2+浓度模型的预测结果进行了比较,在该模型中,Ca2+通过一个点源进入细胞,从进入位点扩散,并与固定或移动的Ca2+缓冲剂结合。当模型将移动分子作为唯一的Ca2+缓冲剂时,在各种条件下观察到的荧光变化的时间进程和幅度都得到了很好的拟合。结果证实了Ca2+在神经递质释放中的局部进入,并表明Ca2+几乎完全通过移动缓冲剂从活性区清除。