Fig. 7.
Fig. 7. Influence of liposomes on degranulation of granulocytes. / Granulocytes were incubated with DMSO (A), with cytochalasin B (0.5 μg/mL)/NfMLP (10−6 M) diluted in DMSO, positive control (B), and with plain liposomes (EPC:EPG:Chol, 1 mM lipid) (C) at 37°C for 30 minutes. Degranulation of MPO from azurophilic granules of neutrophils was measured by registration of the shift of the granulocyte cloud from right to left on the x-axis (decrease of MPO in single neutrophils). Plain EPC:SPS:Chol liposomes and GOLs gave the same results, and incubation with DMSO for 30 minutes had no influence on the signals compared to freshly prepared granulocytes (data not shown).

Influence of liposomes on degranulation of granulocytes.

Granulocytes were incubated with DMSO (A), with cytochalasin B (0.5 μg/mL)/NfMLP (10−6 M) diluted in DMSO, positive control (B), and with plain liposomes (EPC:EPG:Chol, 1 mM lipid) (C) at 37°C for 30 minutes. Degranulation of MPO from azurophilic granules of neutrophils was measured by registration of the shift of the granulocyte cloud from right to left on the x-axis (decrease of MPO in single neutrophils). Plain EPC:SPS:Chol liposomes and GOLs gave the same results, and incubation with DMSO for 30 minutes had no influence on the signals compared to freshly prepared granulocytes (data not shown).

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