Schütz Gerhard J, Axmann Markus, Freudenthaler Susanne, Schindler Hansgeorg, Kandror Kostya, Roder John C, Jeromin Andreas
Institute for Biophysics, University of Linz, A-4040 Linz, Austria.
Microsc Res Tech. 2004 Feb 15;63(3):159-67. doi: 10.1002/jemt.20016.
Trafficking of secretory vesicles along neurites of PC12 cells was visualized by 2D and 3D real-time imaging using fluorescence microscopy. Vesicle motion along distinct pathways was directly seen. From an overlay of individual pathways, the underlying cytoskeletal filament could be imaged at a subwavelength resolution. Continuous vesicle transport was interrupted by periods of diffusive motion with concomitant pathway changes. Statistical analysis shows that such interruptions were distributed stochastically along the filament, indicating a limited processivity of motor proteins also in a cellular context. Periods of diffusive motion facilitated the interaction with actively transported vesicles. Frequent associations and dissociations of vesicles have been observed consistently, pointing to a functional relevance of vesicle cotransport.
利用荧光显微镜通过二维和三维实时成像观察了分泌囊泡沿PC12细胞神经突的运输过程。可以直接看到囊泡沿着不同路径的运动。从各个路径的叠加图像中,可以以亚波长分辨率对潜在的细胞骨架丝进行成像。连续的囊泡运输会被伴有路径变化的扩散运动时期打断。统计分析表明,这种打断在丝上是随机分布的,这表明在细胞环境中运动蛋白的持续性也是有限的。扩散运动时期促进了与主动运输囊泡的相互作用。一直以来都观察到囊泡频繁地结合和解离,这表明囊泡共运输具有功能相关性。