Abstract
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.
Original language | English |
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Pages (from-to) | 159-167 |
Number of pages | 9 |
Journal | Microscopy Research and Technique |
Volume | 63 |
Issue number | 3 |
DOIs | |
Publication status | Published - 15 Feb 2004 |
Keywords
- 3D imaging
- Fluorescence microscopy
- Microtubule
- Motor molecules
- Vesicle sorting
- Vesicle tracking
- Green Fluorescent Proteins
- Rats
- PC12 Cells
- Protein Transport
- Animals
- Luminescent Proteins/genetics
- Neurites/metabolism
- Microscopy, Fluorescence/methods