Figure 5.
Figure 5. HC effect on apoptosis and proliferation of IL-15–activated CD56+CD3– and CD56+CD3+ cells. (A) Total CD56+ cells were cultured with IL-15 in the absence or presence of 10–4 M HC for 7 days and analyzed by FACS, on CD3– and CD3+ gated cells, for 7AAD (dead cells) and annexin V (apoptotic or undergoing apoptosis cells) staining. Results from one representative donor of 3 tested are shown. Numbers in the quadrants represent percentage of positive cells. (B) Sorted CD56+CD3– and (C) CD56+CD3+ cells were cultured with IL-15 for a period of 20 days in the absence (♦) or presence (⋄) of 10–4 M HC. Proliferation of the 2 populations was estimated by [3H]TdR incorporation at the indicated time points. Results represent mean plus or minus SD of triplicate cultures from 2 different donors.

HC effect on apoptosis and proliferation of IL-15–activated CD56+CD3 and CD56+CD3+ cells. (A) Total CD56+ cells were cultured with IL-15 in the absence or presence of 10–4 M HC for 7 days and analyzed by FACS, on CD3 and CD3+ gated cells, for 7AAD (dead cells) and annexin V (apoptotic or undergoing apoptosis cells) staining. Results from one representative donor of 3 tested are shown. Numbers in the quadrants represent percentage of positive cells. (B) Sorted CD56+CD3 and (C) CD56+CD3+ cells were cultured with IL-15 for a period of 20 days in the absence (♦) or presence (⋄) of 10–4 M HC. Proliferation of the 2 populations was estimated by [3H]TdR incorporation at the indicated time points. Results represent mean plus or minus SD of triplicate cultures from 2 different donors.

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