Figure 3.

The effect of tumor necrosis factor-α + interferon-γ + interleukin-1β on CACO-2 transepithelial electrical resistance and transepithelial flux of ¹⁴C-D-mannitol. A: Twenty-one day post-confluent CACO-2 cell layers cultured and treated as described in Figure 1, were refed in control medium or medium containing the combination of 200 ng/mL tumor necrosis factor-α, 150 ng/mL interferon-γ, and 50 ng/mL interleukin-1β. Data shown represent the mean ± SE of 16 cell layers per condition. Data represent the percent of control resistance normalized across 4 experiments; B: Radiotracer flux studies were conducted as described in Figure 1, with the same conditions listed above for panel A. Data represent the percent of control flux rate normalized across 2 experiments, and is expressed as the mean ± SE of 8 cell layers per condition. ^bP < 0.001 vs control (Student’s t test, one-tailed).