Open AccessAnalysis of radiation‐induced apoptosis in human lymphocytes: Flow cytometry using Annexin V and propidium iodide versus the neutral comet assay
Author(s) -
Wilkins R.C.,
Kutzner B.C.,
Truong M.,
SanchezDardon J.,
McLean J.R.N.
Publication year - 2002
Publication title -
cytometry
Language(s) - English
Resource type - Journals
eISSN - 1097-0320
pISSN - 0196-4763
DOI - 10.1002/cyto.10098
Subject(s) - propidium iodide , comet assay , apoptosis , flow cytometry , annexin , microbiology and biotechnology , dna fragmentation , dna damage , fragmentation (computing) , biology , annexin a5 , cytometry , programmed cell death , dna , biochemistry , ecology
Background The neutral comet assay was devised to measure double‐stranded DNA breaks, but it has also been used to measure apoptosis based on its characteristic DNA fragmentation patterns. There is still uncertainty about the reliability of this method. By comparing the comet assay with a flow cytometry method that uses Annexin V binding to apoptotic cells, we have provided further evidence for evaluating the usefulness of the comet assay for detecting apoptosis. Methods Apoptosis was induced in human peripheral blood mononuclear cells (PBMC) by ionizing radiation and measured using the comet assay and a flow cytometry method that measures Annexin V and propidium iodide (PI) staining. Results The Annexin V flow cytometry assay distinguished among early apoptosis, late apoptosis, and an apoptotic or necrotic phase in which the cells were labeled with both Annexin V and PI. The comet assay detected only the latter two phases of apoptosis. Conclusions The comet assay is a useful tool for measuring the late stages of apoptosis whereas the Annexin V assay measures higher amounts of apoptosis because it can detect cells in an earlier stage of the apoptotic pathway. Cytometry 48:14–19, 2002. © 2002 Wiley‐Liss, Inc.