Modeling the Excess Cell Surface Stored in a Complex Morphology of Bleb-Like Protrusions
Fig 3
A. Fluorescence, DIC and merged images of rounded CHO cells stably transfected with Lifeact-GFP. B. Fluorescence, DIC and merged images taken near the equatorial plane of a rounded CHO cell with the fluorescence signal coming from the PH domain of PLC-delta fused to EGFP that marks the inner leaflet of the plasma membrane (Bar = 5 μm). C. Scanning electron microscope image of the rounded state (Bar = 5 μm). D. BLiP radii distribution for N = 7096 BLiPs.