Home LiteratureArticle Details
PMID: 12821680 Published · ppublish English Journal Article

Uncoupling cell shrinkage from apoptosis reveals that Na+ influx is required for volume loss during programmed cell death.

The Journal of biological chemistry ·Vol. 278 ·No. 40 ·2003-10-03 ·Pages 39176-84

Bortner CD, Cidlowski JA

Abstract

Cell shrinkage, or the loss of cell volume, is a ubiquitous characteristic of programmed cell death that is observed in all examples of apoptosis, independent of the death stimulus. This decrease in cell volume occurs in synchrony with other classical features of apoptosis. The molecular basis for cell shrinkage during apoptosis involves fluxes of intracellular ions including K+, Na+, and Cl-. Here we show for the first time that these ion fluxes, but not cell shrinkage, are necessary for apoptosis. Using sodium-substituted medium during anti-Fas treatment of Jurkat cells, we observed cellular swelling, a property normally associated with necrosis, in contrast to the typical cell shrinkage. Surprisingly, these swollen cells displayed all of the other classical features of apoptosis, including chromatin condensation, externalization of phosphatidylserine, caspase activity, poly(ADP)-ribose polymerase cleavage, and internucleosomal DNA degradation. These swollen cells had a marked decrease in intracellular potassium, and subsequent inhibition of this potassium loss completely blocked apoptosis. Reintroduction of sodium ions in cell cultures reversed this cellular swelling, resulting in a dramatic loss of cell volume and the characteristic apoptotic morphology. Additionally, inhibition of sodium influx using a sodium channel blocker saxitoxin completely prevented the onset of anti-Fas-induced apoptosis in Jurkat cells. These findings suggest that sodium influx can control not only changes in cell size but also the activation of apoptosis, whereas potassium ion loss controls the progression of the cell death process. Therefore cell shrinkage can be separated from other features of apoptosis.

MeSH Terms
Adenosine Triphosphate/metabolism Apoptosis Caspases/chemistry Chlorine/chemistry Chromatin/metabolism DNA/metabolism Electrophoresis, Agar Gel Flow Cytometry Humans Ions Jurkat Cells Lipid Metabolism Microscopy, Confocal Microscopy, Fluorescence Necrosis Nucleosomes/metabolism Phosphatidylserines/chemistry Poly(ADP-ribose) Polymerases/chemistry Potassium/chemistry Sodium/chemistry,metabolism
Chemicals
Chromatin Ions Nucleosomes Phosphatidylserines Chlorine Adenosine Triphosphate DNA Sodium Poly(ADP-ribose) Polymerases Caspases Potassium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bortner Carl D
Laboratory of Signal Transduction, NIEHS, Department of Health and Human Services, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.
Cidlowski John A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-10-03
Epub
2003-00-23
Pages
39176-84
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com