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. Author manuscript; available in PMC: 2014 Jun 15.
Published in final edited form as: J Immunol. 2013 May 13;190(12):6434–6449. doi: 10.4049/jimmunol.1202329

Table 3.

Binding of annexin-V and propidium iodide to WT vs. Adam8−/− eosinophils do not differ when the extrinsic apoptosis pathway is triggered in vitro

Time point WT EosinophilsA Adam8−/− Eosinophils WT Eosinophils Adam8−/− Eosinophils WT Eosinophils Adam8−/− Eosinophils

% Apoptotic Cells
Mean (SEM) n
% Apoptotic Cells
Mean (SEM) n
% Late Apoptotic Cells
Mean (SEM) n
% Late Apoptotic Cells
Mean (SEM) n
% Viable Cells
Mean (SEM) n
% Viable Cells
Mean (SEM) n

0 h 0 (2.9) 3B 0 (3.1) 3 0.5 (0.3) 3 0 (0.2) 3 0.3 (2.7) 3 0.2 (3.1) 3
2 h 4.1 (6.4) 3 8.4 (10.6) 3 0.3 (0.1) 3 1.2 (0.5) 3 3.6 (6.3) 3 8.3 (10.7) 3
4 h 19 (5.9) 3 16.7 (6.1) 3 3 (1.3) 3 7.3 (0.7) 3 18.3 (5) 3 19.4 (7) 3
6 h 12.2 (9.3) 3 9.9 (19.3) 3 5.8 (2.5) 3 10.9 (8.4) 3 16.4 (8.2) 3 30.1 (7.8) 3
8 h 19.7 (15) 3 7.3 (2.2) 3 7.5 (1.7) 3 8.2 (0.7) 3 30.2 (8.9) 3 29.5 (6.4) 3
20 h 46.2 (10.9) 3 40.2 (9.6) 3 38.7 (12.5) 3 40.6 (8.9) 3 57.2 (2.1) 3 51.8 (2.6) 3
A

Eosinophils and macrophages were isolated from unchallenged BALB/c WT and BALB/c Adam8−/− mice, as described in Methods. Equal numbers of eosinophils or macrophages were incubated with a cross-linking antibody to CD95 (FAS) which activates this death domain-containing receptor, or a non-immune isotype control antibody for up to 20 h for eosinophils or 48 h for macrophages. At intervals, cells were stained with annexin-V conjugated to Alexa 488 and propidium iodide, and the percentage of cells staining positively and negatively with these reagents was quantified using flow cytometry. The results for cells incubated with a non-immune control antibody were subtracted from those incubated with anti-CD95. We determined the percentages of apoptotic cells (cell staining positively with annexin-V and negatively with propidium iodide), late apoptotic cells (cells staining positively with both annexin-V and propidium iodide), and viable cells (cells not stained with either annexin-V or propidium iodide).

B

Data are mean ± SEM; n = number of independent experiments.

We were not able to induce significant positive staining for either annexin V or propidium iodide in either WT or Adam8−/− macrophages by treating cells with the FAS cross-linking antibody for up to 48 h.