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Journal of Histochemistry and Cytochemistry, Vol. 46, 895-900, August 1998, Copyright © 1998, The Histochemical Society, Inc.
Comparison of Annexin V and Calcein-AM as Early Vital Markers of Apoptosis in Adherent Cells by Confocal Laser Microscopy
Rita Gattia,
Silvana Bellettib,
Guido Orlandinic,
Ovidio Bussolatib,
Valeria Dall'Astab, and
Gian Carlo Gazzolab
a Institute of Histology and General Embryology, University of Parma, Parma, Italy
b Institute of General Pathology, University of Parma, Parma, Italy
c Department of Clinical Medicine and Nephrology, University of Parma, Parma, Italy
Correspondence to:
Rita Gatti, Inst. of Histology and General Embryology, University of Parma, Via Volturno, 39, 43100 Parma, Italy.
Although morphological criteria for apoptosis are in general reliable, no systematic comparison of the techniques employed thus far has yet been performed. In this study, using confocal laser microscopy, we compared the performance of annexin V-FITC and calcein-AM for early detection of apoptosis in living adherent cells. Experiments were carried out on two distinct cell lines, PC 12 and NIH3T3, endowed with different shape and adhesion properties. The apoptotic process was followed for a prolonged period in the same cells of a predetermined field by means of a special flow chamber. Our results show that both probes allowed the detection of apoptotic cells in either cell line. However, some cells that clearly exhibited apoptotic changes on calcein visualization were annexin-negative. In NIH3T3 cells, annexin negativity of apoptotic cells was correlated with the preservation of cell shape and adhesion properties. These findings show that, at least in PC12 and NIH3T3 cells, annexin might be less sensitive than calcein-AM for early apoptosis detection and, for NIH3T3 cells, suggest that phosphatidilserine exposure is in some way linked to changes in cell shape and/or adhesion to culture substrate. (J Histochem Cytochem 46:895900, 1998)
Key Words:
apoptosis, vital dyes, calcein-AM, annexin V-FITC, cell adhesion, confocal laser microscopy, PC 12 cells, NIH3T3 cells

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