Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-29T21:24:12.618Z Has data issue: false hasContentIssue false

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
Get access

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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

1.Chacon, E. et al. FEBS Lett. 382( 1996)31.CrossRefGoogle Scholar
2.Trollingeret, D.R. al. Biochem. Biophys. Res. Commun. 236(1997)738.CrossRefGoogle Scholar
3.Ohata, H. et al. J. Bioenerg. Biomembr. (1998) in press.Google Scholar
4.Trollinger, D.R. et al. Biophys. J. (1998) in press (abstract).Google Scholar