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Calcium-vesicles perform active diffusion in the sea urchin embryo during larval biomineralization

Fig 5

Vesicle tracking reveals an active diffusion motion with higher diffusion coefficient and speed in the skeletogenic cells compared to the ectodermal cells.

(A, B) Examples for the automated tracking used to quantify vesicle kinetics. (A) Instantaneous speed indicates the distance traveled between sequential frames divided by the time interval between the frame. The magenta line demonstrates this distance for the magenta labeled vesicle. (B) Directionality index is the ratio of maximal displacement (white line) over the total distance traveled (magenta line) within a one-minute time interval. A representative 3D movie of tracking session is provided in S9 Movie. (C-E) Comparison of vesicle motion statistics between control and VEGFR inhibited embryos. The total number of vesicle measured in the control skeletogenic cells: 825, ectodermal cells: 4193; VEGFR inhibition skeletogenic cells: 884, ectodermal cells: 4508. Each box plot shows the average (white square), median (middle line), the first and the third quartiles (the 25th and 75th percentiles, edges of boxes) and outliers (black dots). (C) Vesicle instantaneous speed. (D) Directionality index. (E) Vesicle diffusion coefficient. (Dunn-Sidak test, p<0.0001, exact p-values are given in S1 Dataset). (F) Histogram of Diffusion model fit, 90% of vesicle tracks are well modeled by the standard diffusion model (R2>0.8).

Fig 5

doi: https://doi.org/10.1371/journal.pcbi.1008780.g005