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. 2002 Mar;127(3):445–454. doi: 10.1046/j.1365-2249.2002.01769.x

Fig. 8.

Fig. 8

Cytofluorometric analysis of the mitochondrial transmembrane potential (δψm).After the HUVECs were stimulated with or without TNF-α (100 ng/ml) for 6 h, the cells were incubated in the presence (bold lines) and absence (shaded histograms) of IVIG (20 mg/ml) for 24 and 36 h. After the HUVECs were exposed to DiOC6 and analysed by a flow cytometer. The proportion (%) of cells in M1 indicates the loss of δψm, represented by a decrease in the fluorescence (FL1-H). As a positive control, CCCP (50 μm) was able to cause a complete loss of δψm at 0 h (dotted lines). All data are representative of five independent experiments giving similar results. Inline graphic, IVIG (−); —, IVIG (+); …, positive control.