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Confocal Imaging of Both Mitochondrial and Cytosolic Free Ca2+ in Cardiac Myocytes Co-Loaded with Rhod 2 and Fluo 3: Inhibition by Ruthenium Red of Mitochondrial but not Cytosolic Ca2+ Transients

Published online by Cambridge University Press:  02 July 2020

Donna R. Trollinger
Affiliation:
Departments of Cell Biology & Anatomy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7090
Wayne E. Cascio
Affiliation:
Departments of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7090
John J. Lemasters
Affiliation:
Departments of Cell Biology & Anatomy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27599-7090
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Extract

Previously, we showed rapid mitochondrial Ca2+ transients in adult rabbit cardiac myocytes during the contractile cycle. Ruthenium red, an inhibitor of mitochondrial Ca2+ uptake by the Ca2+ uniporter, inhibits mitochondrial Ca2+ transients in adult rabbit cardiac myocytes during electrical stimulation. Here, we extend this finding to show that ruthenium red inhibition is specific for mitochondrial Ca2+ transients and not cytosolic Ca2+ transients.

Ca 2+-tolerant adult rabbit cardiac myocytes were isolated by collagenase and hyaluronidase digestion and loaded in the cold with 2.5 μM Rhod 2-AM for 30 minutes. Subsequently, the cells were incubated in nutrient medium at 37°C for 4-6 hours during which time cytosolic but not mitochondrial Rhod 2 was lost. Subsequently, the myocytes were loaded with 10 μM Fluo 3-AM for 15 minutes at 37°C, conditions that lead to predominantly cytosolic localization of Fluo 3. In sequential scans, the red fluorescence of Rhod 2 and the green fluorescence of Fluo 3 were imaged using a Zeiss LSM 410 laser scanning confocal microscope.

Type
Unique Approaches in Imaging, Computation and Communication for Characterization of the 3D Cell & Organelles I
Copyright
Copyright © Microscopy Society of America

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References

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