Cdc42 and Actin Control Polarized Expression of TI-VAMP Vesicles to Neuronal Growth Cones and Their Fusion with the Plasma Membrane
Mol. Biol. Cell Alberts et al.
17: 1194
Supplemental Material
This article contains the following supporting material:
Movie 1
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Exocytosis of TIV-pHL vesicles and tubules
A Cos7 cell transfected with TIV-pHL was imaged at 30 images/min with an exposure time of 400ms per frame for a total of 9min 42sec. Numerous circular puffs of light appear for a few seconds each. Several worm-like structures corresponding to the fusion of tubules are also seen (at 4min 06sec, for instance).
Movie 2
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The exocytosis of TI-VAMP is positively regulated by Cdc42
Cos7 cells were cotransfected with TIV-pHL and RFP (left cell) or with Cdc42V12-RFP (right cell) and imaged for 6 min. 18sec. There is a high increase in the number of exocytic events in the cell coexpressing TIV-pHL and Cdc42V12-RFP compared to the cell coexpressing TIV-pHL and RFP.
Movie 3
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The stimulatory effect of Cdc42-V12-RFP on exocytosis is F-actin-dependent
A Cos7 cell cotransfected with Cdc42V12-RFP and TIV-pHL was imaged before (left) and 15min. after treatment with 5µM cytochalasin B (right) for 6min 26 sec each. Cytochalasin B strongly inhibits the number of exocytic events (compare exocytic activity in the right panel with the left panel).