Figure 3—source data 1.

Figure 3—source data 1.

(a) Mapping of the trajectory of a single mitochondrion (black arrow) onto the inverted wide-field images (scale bar, 5 µm). Bottom panel, kymograph color coded according to motion state, location of stationary mitochondria depicted in gray. (b) Pie charts indicating the fraction of time spent in each motion state related to the local presence or absence of a mitochondrion in retrograde (left) or anterograde (right) direction (n = 16 trajectories, nine fish). (c) Repetitive tracking of mitochondria over the same stretch of an axon. Upper Panel: Wide field image of the ROI showing the location of stalled mitochondria on a section of microtubules. Middle panel: The time a mitochondrion needed to transverse 100 nm is plotted as a function of position along the axon. Gray boxes indicate the presence of stationary mitochondria. The red line indicates the threshold level to identify bins of slow movement. Dashed black lines indicate locations where multiple mitochondria were observed to pause (see lower panel). Lower panel: Fraction of trajectories (plotted in 1 µm bins from mitochondria moving in both directions) along the axon showing crossing times of more than 10 s for 1 µm.

10.7554/eLife.46059.021Figure 3—source data 1.