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Difference between revisions of "Kalbacova 2003 Cytometry"

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(Created page with "{{Publication |title=Kalbacova M, Vrbacky M, Drahota Z, Melkova Z (2003) Comparison of the effect of mitochondrial inhibitors on mitochondrial membrane potential in two different...")
 
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|abstract=Background: Determination of mitochondrial membrane
|abstract=Background: Determination of mitochondrial membrane
potential ((m) is widely used to characterize cellular
potential ((m) is widely used to characterize cellular
metabolism, viability, and apoptosis. Changes of ��m
metabolism, viability, and apoptosis. Changes of ΔΨm
induced by inhibitors of oxidative phosphorylation characterize
induced by inhibitors of oxidative phosphorylation characterize
respective contributions of mitochondria and glycolysis
respective contributions of mitochondria and glycolysis
to adenosine triphosphate (ATP) synthesis.
to adenosine triphosphate (ATP) synthesis.
Methods: ��m in BSC-40 and HeLa G cell lines was
Methods: ΔΨm in BSC-40 and HeLa G cell lines was
determined by flow cytometry and spectrofluorometry. Its
determined by flow cytometry and spectrofluorometry. Its
changes induced by specific mitochondrial inhibitors
changes induced by specific mitochondrial inhibitors
were evaluated using 3,3�-dihexyloxacarbocyanine iodide
were evaluated using 3,3ΔΨ-dihexyloxacarbocyanine iodide
(DiOC6(3)), tetramethylrhodamine ethyl ester, and Mito-
(DiOC6(3)), tetramethylrhodamine ethyl ester, and Mito-
Tracker Red. Mitochondrial function was further characterized
Tracker Red. Mitochondrial function was further characterized
by oxygen consumption.
by oxygen consumption.
Results: Inhibition of respiration by antimycin A or uncoupling
Results: Inhibition of respiration by antimycin A or uncoupling
of mitochondria by FCCP decreased ��m in
of mitochondria by FCCP decreased ΔΨm in
both cell lines. Inhibition of ATP production by oligomycin
both cell lines. Inhibition of ATP production by oligomycin
or atractyloside induced a moderate decrease of ��m
or atractyloside induced a moderate decrease of ΔΨm
in HeLa G cells and an increase of ��m in BSC-40 cells.
in HeLa G cells and an increase of ΔΨm in BSC-40 cells.
Statistically significant differences in ��m between the
Statistically significant differences in ΔΨm between the
two cell lines were found with both flow cytometry and
two cell lines were found with both flow cytometry and
spectrofluorometry. Respirometry showed higher basal
spectrofluorometry. Respirometry showed higher basal
and FCCP-stimulated respiration in BSC-40 cells.
and FCCP-stimulated respiration in BSC-40 cells.
Conclusion: Changes of ��m and oxygen consumption
Conclusion: Changes of ΔΨm and oxygen consumption
showed that BSC-40 cells are more sensitive than HeLa G
showed that BSC-40 cells are more sensitive than HeLa G
cells to inhibitors of mitochondrial function, suggesting
cells to inhibitors of mitochondrial function, suggesting
that BSC-40 cells are more dependent than HeLa G cells on
that BSC-40 cells are more dependent than HeLa G cells on
aerobic ATP production. Determination of ��m changes
aerobic ATP production. Determination of ΔΨm changes
by flow cytometry exhibited greater sensitivity than the
by flow cytometry exhibited greater sensitivity than the
ones by spectrofluorometry. Cytometry Part A 52A:
ones by spectrofluorometry. Cytometry Part A 52A:

Revision as of 16:23, 4 October 2010

Publications in the MiPMap
Kalbacova M, Vrbacky M, Drahota Z, Melkova Z (2003) Comparison of the effect of mitochondrial inhibitors on mitochondrial membrane potential in two different cell lines using flow cytometry and spectrofluorometry. Cytometry 52A: 110-116.

» PMID: 12655654

Kalbacova M, Vrbacky M, Drahota Z, Melkova Z (2003)

Abstract: Background: Determination of mitochondrial membrane potential ((m) is widely used to characterize cellular metabolism, viability, and apoptosis. Changes of ΔΨm induced by inhibitors of oxidative phosphorylation characterize respective contributions of mitochondria and glycolysis to adenosine triphosphate (ATP) synthesis. Methods: ΔΨm in BSC-40 and HeLa G cell lines was determined by flow cytometry and spectrofluorometry. Its changes induced by specific mitochondrial inhibitors were evaluated using 3,3ΔΨ-dihexyloxacarbocyanine iodide (DiOC6(3)), tetramethylrhodamine ethyl ester, and Mito- Tracker Red. Mitochondrial function was further characterized by oxygen consumption. Results: Inhibition of respiration by antimycin A or uncoupling of mitochondria by FCCP decreased ΔΨm in both cell lines. Inhibition of ATP production by oligomycin or atractyloside induced a moderate decrease of ΔΨm in HeLa G cells and an increase of ΔΨm in BSC-40 cells. Statistically significant differences in ΔΨm between the two cell lines were found with both flow cytometry and spectrofluorometry. Respirometry showed higher basal and FCCP-stimulated respiration in BSC-40 cells. Conclusion: Changes of ΔΨm and oxygen consumption showed that BSC-40 cells are more sensitive than HeLa G cells to inhibitors of mitochondrial function, suggesting that BSC-40 cells are more dependent than HeLa G cells on aerobic ATP production. Determination of ΔΨm changes by flow cytometry exhibited greater sensitivity than the ones by spectrofluorometry. Cytometry Part A 52A: 110–116, 2003.


Labels:

Stress:Cancer; Apoptosis; Cytochrome c"Cancer; Apoptosis; Cytochrome c" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property. 

Tissue;cell: Blood Cell; Suspension Culture"Blood Cell; Suspension Culture" is not in the list (Heart, Skeletal muscle, Nervous system, Liver, Kidney, Lung;gill, Islet cell;pancreas;thymus, Endothelial;epithelial;mesothelial cell, Blood cells, Fat, ...) of allowed values for the "Tissue and cell" property. 


Regulation: Respiration; OXPHOS; ETS Capacity"Respiration; OXPHOS; ETS Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., Coupling; Membrane Potential"Coupling; Membrane Potential" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., Ion Homeostasis"Ion Homeostasis" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property., Substrate; Glucose; TCA Cycle"Substrate; Glucose; TCA Cycle" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property. 


HRR: Oxygraph-2k, Spectrophotometry; Spectrofluorimetry"Spectrophotometry; Spectrofluorimetry" is not in the list (Oxygraph-2k, TIP2k, O2k-Fluorometer, pH, NO, TPP, Ca, O2k-Spectrophotometer, O2k-Manual, O2k-Protocol, ...) of allowed values for the "Instrument and method" property.