Video-rate far-field optical nanoscopy dissects synaptic vesicle movement

被引:599
作者
Westphal, Volker [1 ]
Rizzoli, Silvio O. [2 ,3 ]
Lauterbach, Marcel A. [1 ]
Kamin, Dirk [3 ]
Jahn, Reinhard [2 ]
Hell, Stefan W. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Nanobiophoton, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Neurobiol, D-37077 Gottingen, Germany
[3] European Neurosci Inst, STED Microscopy Synapt Funct, D-37077 Gottingen, Germany
关键词
D O I
10.1126/science.1154228
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We present video-rate (28 frames per second) far-field optical imaging with a focal spot size of 62 nanometers in living cells. Fluorescently labeled synaptic vesicles inside the axons of cultured neurons were recorded with stimulated emission depletion (STED) microscopy in a 2.5-micrometer by 1.8-micrometer field of view. By reducing the cross-sectional area of the focal spot by about a factor of 18 below the diffraction limit (260 nanometers), STED allowed us to map and describe the vesicle mobility within the highly confined space of synaptic boutons. Although restricted within boutons, the vesicle movement was substantially faster in nonbouton areas, consistent with the observation that a sizable vesicle pool continuously transits through the axons. Our study demonstrates the emerging ability of optical microscopy to investigate intracellular physiological processes on the nanoscale in real time.
引用
收藏
页码:246 / 249
页数:4
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