Skip to main content
. Author manuscript; available in PMC: 2021 May 1.
Published in final edited form as: J Cell Physiol. 2019 Oct 14;235(5):4351–4360. doi: 10.1002/jcp.29311

Figure 3. Compensatory endocytosis in activated eggs requires actin cytoskeleton dynamics and dynamin.

Figure 3.

Quantification of internalized fluorescent labeling after pulse-chase experiments in the presence of 10 μM CytD,10 μM LatA or 0.5 μM Jas (A), 5 μM filipin (B), 15 μM PitStop 2 (C) or 80 μM dynasore (D). The number of internalized fluorescent dots was relativized to control (-, DMSO). Inhibitors were added during pulse to prevent possible deleterious effects on cortical exocytosis. The total number of evaluated eggs for each group is shown in brackets. *p<0.05, **p<0.01.