A membrane marker leaves synaptic vesicles in milliseconds after exocytosis in retinal bipolar cells

被引:148
作者
Zenisek, D
Steyer, JA
Feldman, ME
Almers, W [1 ]
机构
[1] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
[2] Univ Calif Berkeley, Dept Biol, Berkeley, CA 94720 USA
[3] Cornell Univ, Dept Biomed Sci, Ithaca, NY 14853 USA
[4] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
关键词
D O I
10.1016/S0896-6273(02)00896-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Perhaps synaptic vesicles can recycle so rapidly because they avoid complete exocytosis, and release transmitter through a fusion pore that opens transiently. This view emerges from imaging whole terminals where the fluorescent lipid FM1-43 seems unable to leave vesicles during transmitter release. Here we imaged single, FM1-43-stained synaptic vesicles by evanescent field fluorescence microscopy, and tracked the escape of dye from single vesicles by watching the increase in fluorescence after exocytosis. Dye left rapidly and completely during most or all exocytic events. We conclude that vesicles at this terminal allow lipid exchange soon after exocytosis, and lose their dye even if they connected with the plasma membrane only briefly. At the level of single vesicles, therefore, observations with FM1-43 provide no evidence that exocytosis of synaptic vesicles is incomplete.
引用
收藏
页码:1085 / 1097
页数:13
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