Fig. 2.
Fig. 2. Effect of interaction between either monocytes or endothelial cells and K562 cells on secretion of IL-8 from endothelial cells. Monocytes (1 × 106 cells/mL) and human umbilical venous cells (VE cells, confluent) were cultured with or without K562 cells (5 × 104 cells/mL) for 2 days, and supernatants were then collected. (A) ELISA system for IL-8 was performed. Columns show the means of three independent experiments. Statistical analysis was performed using the Student’s t-test. (B) When VE cells were cocultured with (right) or without (left) K562 cells, the remaining VE cells, after removal of K562 cells, were collected and expression of intracytoplasmic IL-8 was examined as described in Materials and Methods. Purified mouse Ig G1 was used as a control antibody (CONTROL). The vertical axis indicates the frequency of fluorescence-positive cells. Intracytoplasmic IL-8 density is depicted on the horizontal axis. The representative data from three independent experiments are shown.

Effect of interaction between either monocytes or endothelial cells and K562 cells on secretion of IL-8 from endothelial cells. Monocytes (1 × 106 cells/mL) and human umbilical venous cells (VE cells, confluent) were cultured with or without K562 cells (5 × 104 cells/mL) for 2 days, and supernatants were then collected. (A) ELISA system for IL-8 was performed. Columns show the means of three independent experiments. Statistical analysis was performed using the Student’s t-test. (B) When VE cells were cocultured with (right) or without (left) K562 cells, the remaining VE cells, after removal of K562 cells, were collected and expression of intracytoplasmic IL-8 was examined as described in Materials and Methods. Purified mouse Ig G1 was used as a control antibody (CONTROL). The vertical axis indicates the frequency of fluorescence-positive cells. Intracytoplasmic IL-8 density is depicted on the horizontal axis. The representative data from three independent experiments are shown.

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