Characterization of cells with different mitochondrial membrane potential during apoptosis

Enrico Lugli, Leonarda Troiano, Roberta Ferraresi, Erika Roat, Nicole Prada, Milena Nasi, Marcello Pinti, Edwin L. Cooper, Andrea Cossarizza

Research output: Contribution to journalArticle

92 Citations (Scopus)

Abstract

Background: Until now, the simultaneous analysis of several parameters during apoptosis, including DNA content and mitochondrial membrane potential (ΔΨ), has not been possible because of the spectral characteristics of the commonly used dyes. Using polychromatic flow cytometry based upon multiple laser and UV lamp excitation, we have characterized cells with different ΔΨ during apoptosis. Methods: U937 cells were treated with the flavonoid quercetin (Qu) and stained with JC-1 to detect ΔΨ, propidium iodide (PI) for cell viability, Hoechst 33342 for DNA content, Annexin V conjugated with Alexa Fluor-647 for detection of phosphatidilserine (PS) exposure, marker of early apoptosis, or Mitotracker Deep Red for the determination of mitochondrial mass. Results: Treatment with Qu provoked the onset of three cell populations with different ΔΨ: (1) healthy cells, with normal ΔΨ, DNA content and physical parameters, high mitochondrial mass, PI- and Annexin V-negative; (2) cells with intermediate ΔΨ and normal DNA content, but with physical parameters typical of apoptotic cells and low mitochondrial mass; most of them were PI+ and Annexin V+; (3) cells with collapsed ΔΨ that had low mitochondrial mass and were Annexin-V+, PI+; half of them showed diminished DNA content. Similar results, i.e. the presence of cells with intermediate ΔΨ, were observed in other models of apoptosis. Conclusions: During Qu-induced apoptosis, loss of ΔΨ, PS exposure, and decrease of mitochondrial mass are early events that precede permeability to PI and loss of DNA. Populations of cells with different ΔΨ, as revealed by flow cytometry after JC-1 staining, differed also for other parameters associated to apoptosis. Thus, the simultaneous analysis of several parameters by polychromatic flow cytometry permits a better identification of many stages of cell death, and, more in general, allows to evaluate the eventual heterogenic sensibility of the population under study to a given compound.

Original languageEnglish
Pages (from-to)28-35
Number of pages8
JournalCytometry Part A
Volume68
Issue number1
DOIs
Publication statusPublished - Nov 2005

Fingerprint

Mitochondrial Membrane Potential
Propidium
Apoptosis
Annexin A5
DNA
Quercetin
Flow Cytometry
Population
U937 Cells
Flavonoids
Permeability
Cell Survival
Lasers
Cell Death
Coloring Agents
Staining and Labeling

Keywords

  • Annexin-V
  • Apoptosis
  • Hoechst
  • JC-1
  • Mitochondrial membrane potential
  • Polychromatic flow cytometry
  • Propidium iodide

ASJC Scopus subject areas

  • Hematology
  • Cell Biology
  • Pathology and Forensic Medicine
  • Biophysics
  • Endocrinology

Cite this

Lugli, E., Troiano, L., Ferraresi, R., Roat, E., Prada, N., Nasi, M., ... Cossarizza, A. (2005). Characterization of cells with different mitochondrial membrane potential during apoptosis. Cytometry Part A, 68(1), 28-35. https://doi.org/10.1002/cyto.a.20188

Characterization of cells with different mitochondrial membrane potential during apoptosis. / Lugli, Enrico; Troiano, Leonarda; Ferraresi, Roberta; Roat, Erika; Prada, Nicole; Nasi, Milena; Pinti, Marcello; Cooper, Edwin L.; Cossarizza, Andrea.

In: Cytometry Part A, Vol. 68, No. 1, 11.2005, p. 28-35.

Research output: Contribution to journalArticle

Lugli, E, Troiano, L, Ferraresi, R, Roat, E, Prada, N, Nasi, M, Pinti, M, Cooper, EL & Cossarizza, A 2005, 'Characterization of cells with different mitochondrial membrane potential during apoptosis', Cytometry Part A, vol. 68, no. 1, pp. 28-35. https://doi.org/10.1002/cyto.a.20188
Lugli, Enrico ; Troiano, Leonarda ; Ferraresi, Roberta ; Roat, Erika ; Prada, Nicole ; Nasi, Milena ; Pinti, Marcello ; Cooper, Edwin L. ; Cossarizza, Andrea. / Characterization of cells with different mitochondrial membrane potential during apoptosis. In: Cytometry Part A. 2005 ; Vol. 68, No. 1. pp. 28-35.
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abstract = "Background: Until now, the simultaneous analysis of several parameters during apoptosis, including DNA content and mitochondrial membrane potential (ΔΨ), has not been possible because of the spectral characteristics of the commonly used dyes. Using polychromatic flow cytometry based upon multiple laser and UV lamp excitation, we have characterized cells with different ΔΨ during apoptosis. Methods: U937 cells were treated with the flavonoid quercetin (Qu) and stained with JC-1 to detect ΔΨ, propidium iodide (PI) for cell viability, Hoechst 33342 for DNA content, Annexin V conjugated with Alexa Fluor-647 for detection of phosphatidilserine (PS) exposure, marker of early apoptosis, or Mitotracker Deep Red for the determination of mitochondrial mass. Results: Treatment with Qu provoked the onset of three cell populations with different ΔΨ: (1) healthy cells, with normal ΔΨ, DNA content and physical parameters, high mitochondrial mass, PI- and Annexin V-negative; (2) cells with intermediate ΔΨ and normal DNA content, but with physical parameters typical of apoptotic cells and low mitochondrial mass; most of them were PI+ and Annexin V+; (3) cells with collapsed ΔΨ that had low mitochondrial mass and were Annexin-V+, PI+; half of them showed diminished DNA content. Similar results, i.e. the presence of cells with intermediate ΔΨ, were observed in other models of apoptosis. Conclusions: During Qu-induced apoptosis, loss of ΔΨ, PS exposure, and decrease of mitochondrial mass are early events that precede permeability to PI and loss of DNA. Populations of cells with different ΔΨ, as revealed by flow cytometry after JC-1 staining, differed also for other parameters associated to apoptosis. Thus, the simultaneous analysis of several parameters by polychromatic flow cytometry permits a better identification of many stages of cell death, and, more in general, allows to evaluate the eventual heterogenic sensibility of the population under study to a given compound.",
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AU - Nasi, Milena

AU - Pinti, Marcello

AU - Cooper, Edwin L.

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N2 - Background: Until now, the simultaneous analysis of several parameters during apoptosis, including DNA content and mitochondrial membrane potential (ΔΨ), has not been possible because of the spectral characteristics of the commonly used dyes. Using polychromatic flow cytometry based upon multiple laser and UV lamp excitation, we have characterized cells with different ΔΨ during apoptosis. Methods: U937 cells were treated with the flavonoid quercetin (Qu) and stained with JC-1 to detect ΔΨ, propidium iodide (PI) for cell viability, Hoechst 33342 for DNA content, Annexin V conjugated with Alexa Fluor-647 for detection of phosphatidilserine (PS) exposure, marker of early apoptosis, or Mitotracker Deep Red for the determination of mitochondrial mass. Results: Treatment with Qu provoked the onset of three cell populations with different ΔΨ: (1) healthy cells, with normal ΔΨ, DNA content and physical parameters, high mitochondrial mass, PI- and Annexin V-negative; (2) cells with intermediate ΔΨ and normal DNA content, but with physical parameters typical of apoptotic cells and low mitochondrial mass; most of them were PI+ and Annexin V+; (3) cells with collapsed ΔΨ that had low mitochondrial mass and were Annexin-V+, PI+; half of them showed diminished DNA content. Similar results, i.e. the presence of cells with intermediate ΔΨ, were observed in other models of apoptosis. Conclusions: During Qu-induced apoptosis, loss of ΔΨ, PS exposure, and decrease of mitochondrial mass are early events that precede permeability to PI and loss of DNA. Populations of cells with different ΔΨ, as revealed by flow cytometry after JC-1 staining, differed also for other parameters associated to apoptosis. Thus, the simultaneous analysis of several parameters by polychromatic flow cytometry permits a better identification of many stages of cell death, and, more in general, allows to evaluate the eventual heterogenic sensibility of the population under study to a given compound.

AB - Background: Until now, the simultaneous analysis of several parameters during apoptosis, including DNA content and mitochondrial membrane potential (ΔΨ), has not been possible because of the spectral characteristics of the commonly used dyes. Using polychromatic flow cytometry based upon multiple laser and UV lamp excitation, we have characterized cells with different ΔΨ during apoptosis. Methods: U937 cells were treated with the flavonoid quercetin (Qu) and stained with JC-1 to detect ΔΨ, propidium iodide (PI) for cell viability, Hoechst 33342 for DNA content, Annexin V conjugated with Alexa Fluor-647 for detection of phosphatidilserine (PS) exposure, marker of early apoptosis, or Mitotracker Deep Red for the determination of mitochondrial mass. Results: Treatment with Qu provoked the onset of three cell populations with different ΔΨ: (1) healthy cells, with normal ΔΨ, DNA content and physical parameters, high mitochondrial mass, PI- and Annexin V-negative; (2) cells with intermediate ΔΨ and normal DNA content, but with physical parameters typical of apoptotic cells and low mitochondrial mass; most of them were PI+ and Annexin V+; (3) cells with collapsed ΔΨ that had low mitochondrial mass and were Annexin-V+, PI+; half of them showed diminished DNA content. Similar results, i.e. the presence of cells with intermediate ΔΨ, were observed in other models of apoptosis. Conclusions: During Qu-induced apoptosis, loss of ΔΨ, PS exposure, and decrease of mitochondrial mass are early events that precede permeability to PI and loss of DNA. Populations of cells with different ΔΨ, as revealed by flow cytometry after JC-1 staining, differed also for other parameters associated to apoptosis. Thus, the simultaneous analysis of several parameters by polychromatic flow cytometry permits a better identification of many stages of cell death, and, more in general, allows to evaluate the eventual heterogenic sensibility of the population under study to a given compound.

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