Fig. 6.
Fig. 6. Killing of. / S aureus by normal and CGD granulocytes. Cells (5 × 105) were incubated at 37°C with S aureus (5 × 105) with and without liposome treatment. GOLs (EPC:SPS:Chol, panel A, and EPC:EPG:Chol, panel B, both 4:3:3 mole ratio, lipid concentration 1 mM) were mixed with granulocytes. Incubation was carried out in the continuous presence of GOLs or after a 15-minute preincubation and subsequent removal of nonphagocytosed GOLs before bacteria were added. Values were set as 100% at the start (0 hours). Shown are the mean values of 3 independent experiments in duplicates (CV [coefficient of variation] < 0.27); ▪ indicates normal granulocytes; ●, CGD granulocytes (both without liposome treatment); ▴, liposomes; ▾, CGD granulocytes with continuous incubation of liposomes; ♦, CGD granulocytes preincubated with liposomes. Results of 2-groupt test are marked with asterisk; P < .05.

Killing of

S aureus by normal and CGD granulocytes. Cells (5 × 105) were incubated at 37°C with S aureus (5 × 105) with and without liposome treatment. GOLs (EPC:SPS:Chol, panel A, and EPC:EPG:Chol, panel B, both 4:3:3 mole ratio, lipid concentration 1 mM) were mixed with granulocytes. Incubation was carried out in the continuous presence of GOLs or after a 15-minute preincubation and subsequent removal of nonphagocytosed GOLs before bacteria were added. Values were set as 100% at the start (0 hours). Shown are the mean values of 3 independent experiments in duplicates (CV [coefficient of variation] < 0.27); ▪ indicates normal granulocytes; ●, CGD granulocytes (both without liposome treatment); ▴, liposomes; ▾, CGD granulocytes with continuous incubation of liposomes; ♦, CGD granulocytes preincubated with liposomes. Results of 2-groupt test are marked with asterisk; P < .05.

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