Skip to main content
. 2018 Aug 6;7:e36456. doi: 10.7554/eLife.36456

Figure 5. Pk2 is dynamically enriched at shrinking V-junctions.

(A) Confocal images of neural epithelial cells labeled with membraneRFP (pseudocolored blue) and GFP-Pk2 showing the change in length of shrinking junctions (inward facing arrowheads) and growing junctions (outward facing arrows) along with the corresponding change in GFP-Pk2 intensity at two different time points. Scale = 10 µm (B) Higher magnification view of the horizontal junctions shown in A, shown at 5-min intervals. Red brackets indicated shrinking junctions; yellow brackets indicate growing junctions. Scale = 10 µm (C) Plots of intensity (red/yellow traces) and length (black dashed traces) for each of the indicated junctions in Panel B. Plots show 30 min of junction dynamics ending in either junction resolution or junction formation and expansion; gray area behind select data points indicate the interval of the four frames shown in (B), which are offset due to different junctions appearing and resolving at different times.

Figure 5.

Figure 5—figure supplement 1. Distinct Vangl2 dynamics at adjacent growing and shrinking junctions.

Figure 5—figure supplement 1.

(A) Confocal stills of a neural epithelium mosaically labeled with GFP-Vangl2 (left) and co-labeled with H2B-RFP and membraneBFP merged with the DIC image (right). White lines indicate junctions of unlabeled neighboring cells. Colored arrows indicate shrinking (orange, green) or growing (blue, purple) behaviors of adjoined cell-cell junctions. Note dramatic changes of Vangl2 intensity at shrinking junctions only. Scale = 10 µm.