Induction of caspase-3 activation determined by immunostaining. Flow
cytometric analyses of PBMCs untreated or treated with anti-Fas mAb
CH11, FasL, or HIV-1 JRFL envelope are shown in A.
Additional results are presented in B with HIV-1 NL43
and 92Ug20.9 envelopes and with anti-Fas mAb CH11. In the histograms in
A, mean channel fluorescence (mcf) is displayed on the
x axis and total cell counts on the y
axis; the gate was set on the CD3+ population. The dotted
line represents unstained cells, the solid line represents the isotype
control, and the shaded areas show anti-active caspase-3 staining. The
marker boundary (M1) was set to exclude background staining in the
untreated cells (Top); the percentage of cells with mcf
values above the marker boundary is indicated in each histogram.
(B) mcf values over background are presented as
determined for A.