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Updated: Aug 10, 2026
Detection and Isolation of Apoptotic Bodies to High Purity
Published on: August 12, 2018
Accurate apoptosis measurement requires quantification of loss of expression of surface antigens and cell
David Diaz1, Alfredo Prieto, Hugo Barcenilla
1CNB-CSIC R&D Associated Unit, Department of Medicine, University of Alcalá, Alcalá de Henares, Madrid, Spain.
Background:
The use of ratiometric cell enumeration methods emerges as a more accurate method of measurement of the occurrence of apoptosis in cell cultures. These new flow cytometry methods were used to quantify the impact of cell fragmentation and loss of lineage antigen (LAg) expression on measurement of apoptosis.
Methods:
Highly purified human lymphocyte populations were negatively sorted and cultured for 24 h. Apoptotic cells were identified using annexin V, 7-amino-actinomycin D and their LAgs were stained with antibodies. A new indicator, the apoptotic rate, was used to determine apoptosis occurrence and its validity compared with the widely accepted percentage of apoptotic cells (apoptotic index, AI).
Results:
Loss of LAg expression and cell fragmentation were observed under all conditions assayed and for all cell populations studied.
Conclusions:
Current methods for quantifying of apoptosis involving AI systematically underestimate apoptosis occurrence in all populations and conditions, especially among cells undergoing spontaneous apoptosis.
