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QuickTime Video JPEG Image

Movie 1

This time-lapse movie shows two Xenopus laevis embryos going through first cleavage. The embryo on the right retains its eggshell (vitelline envelope), and so divides normally, with the two daughter blastomeres clinging tightly together. The embryo on the left has had its vitelline envelope removed, and so it sags onto substrate, exposing the unpigmented, newly inserted basolateral surface as cell division proceeds. This membrane-expansion process can be blocked with nocodazole, which indicates a requirement for microtubules in the process.



QuickTime Video JPEG Image

Movie 2

This time-lapse confocal movie shows vesicles exocytosing onto the surface of a cytochalasin-B-treated Xenopus embryo (same individual as shown in Figs 6 and 7). Vesicles are about 2 mm in diameter, and appear as small spheroids grouped in clusters just under the surface. Frames were 1.8 seconds apart, and so some of these vesicles apparently were open as stable fusion pores for as much as 150 seconds before completing exocytosis. As individual vesicles flatten during exocytosis, they each abruptly add about 20 mm2 of unlabeled membrane to the surface, as indicated by the dark irregular patches quickly diffusing into the surrounding labeled membrane. Notice many of the exocytotic events are clustered (particularly near the top-left corner), even though the surface itself flows rapidly past the field in view.









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