We used quantitative multiparameter how cytometric assays to simultaneously
detect viable, apoptotic, and necrotic human peripheral blood mononuclear
cells (PBMC) and immunophenotyped lymphocyte subsets within the PBMC. Apopt
osis was induced by a spectrum of treatments, including camptothecin, cispl
atin, dexamethasone, hyperthermia, staurosporine, and etoposide in anti-CD3
mAb-stimulated cells and by cyclohexamide in both quiescent and stimulated
cells; apoptosis in the latter was augmented by anti-fas mAb. We found tha
t CD4(+) and CD8(+) cells were significantly underrepresented in the apopto
tic PBMC and that the percentage of CD4(+) and CD8(+) PBMC each markedly de
creased as apoptosis increased. This suggested that surface expression of t
hese receptors was lessened on apoptotic CD4(+) and CD8(+) cells. This was
directly confirmed by observation of sorted CD4(+) PBMC. This analysis of a
wide variety of apoptotic stimuli demonstrates that diminished CD4(+) and
CD8 surface receptor expression is a common feature of human T lymphocyte a
poptosis. (C) 1999 Academic Press.