Stage-Specific Changes in the Water, Na+, Cl- and K+ Contents of Organelles during Apoptosis, Demonstrated by a Targeted Cryo Correlative Analytical Approach

PLoS One. 2016 Feb 11;11(2):e0148727. doi: 10.1371/journal.pone.0148727. eCollection 2016.

Abstract

Many studies have demonstrated changes in the levels of several ions during apoptosis, but a few recent studies have reported conflicting results concerning the changes in water content in apoptotic cells. We used a correlative light and cryo-scanning transmission electron microscopy method to quantify water and ion/element contents simultaneously at a nanoscale resolution in the various compartments of cells, from the onset to the end of apoptosis. We used stably transfected HeLa cells producing H2B-GFP to identify the stages of apoptosis in cells and for a targeted elemental analysis within condensed chromatin, nucleoplasm, mitochondria and the cytosol. We found that the compartments of apoptotic cells contained, on average, 10% more water than control cells. During mitochondrial outer membrane permeabilization, we observed a strong increase in the Na+ and Cl- contents of the mitochondria and a strong decrease in mitochondrial K+ content. During the first step in apoptotic volume decrease (AVD), Na+ and Cl- levels decreased in all cell compartments, but remained higher than those in control cells. Conversely, during the second step of AVD, Na+ and Cl- levels increased considerably in the nucleus and mitochondria. During these two steps of AVD, K+ content decreased steadily in all cell compartments. We also determined in vivo ion status during caspase-3 activity and chromatin condensation. Finally, we found that actinomycin D-tolerant cells had water and K+ contents similar to those of cells entering apoptosis but lower Na+ and Cl- contents than both cells entering apoptosis and control cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anions / analysis
  • Apoptosis* / drug effects
  • Caspase 3 / analysis
  • Cations / analysis
  • Cell Membrane Permeability
  • Cell Size
  • Chlorides / analysis*
  • Cryoelectron Microscopy / methods*
  • Cytochromes c / analysis
  • Dactinomycin / pharmacology
  • HeLa Cells
  • Humans
  • Image Processing, Computer-Assisted
  • Microscopy, Electron, Scanning / methods
  • Mitochondria / chemistry
  • Mitochondrial Membranes
  • Nanotechnology / methods*
  • Organelles / chemistry*
  • Poly Adenosine Diphosphate Ribose / analysis
  • Potassium / analysis*
  • Sodium / analysis*
  • Spectrometry, X-Ray Emission / methods*
  • Time-Lapse Imaging / methods*
  • Water / analysis*

Substances

  • Anions
  • Cations
  • Chlorides
  • Water
  • Dactinomycin
  • Poly Adenosine Diphosphate Ribose
  • Cytochromes c
  • Sodium
  • CASP3 protein, human
  • Caspase 3
  • Potassium

Grants and funding

This work was supported by INSERM (www.inserm.fr) (Physicancer program: Noci-cytox); and Région Champagne Ardenne.(www.cr-champagne-ardenne.fr). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.