Mitochondrial transport in processes of cortical neurons is independent of intracellular calcium
Am J Physiol Cell Physiol Beltran-Parrazal et al.
291: C1193
Supplemental Movies
Five movies in MPG format.
Files in this Data Supplement:
Movie 1a
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Time-lapse sequence of a 4-minute recording of Fluo-4 and MitoTracker fluorescence in a cortical neuron. Mitochondria are observed as punctate fluorescent structures, whereas cytosolic Ca2+ transients caused by spontaneous firing of action potentials can be observed as increases in the background fluorescence of the entire neuron. Mitochondrial movement is not affected by the Ca2+ transients.
Movie 1b
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Same recording as in 1A but with fluorescence represented with an inverse grayscale, so that mitochondria are dark, and calcium transients appear as dark flashes in the entire neuron.
Movie 2a
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Second example of time-lapse sequence of a 6 minute recording of Fluo-4 and MitoTracker fluorescence in a cortical neuron. Again, mitochondrial movement is not affected by transient increases in Ca2+i associated with action potential firing.
Movie 2b
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Same recording as in 2A but with inverse grayscale.
Movie 4
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High magnification sequence showing Fluo-4 and MitoTracker fluorescence in a single dendrite of a cortical neuron as in Figure 4b. Time lapse sequence of a 90 second recording shows the same mitochondrian as the kymograph in 4a. The movement of the mitochondrian is unaffected by multiple spontaneous Ca2+ transients.