Table 2 Effect of Media Composition on MDCK Barrier Function. Confluent MDCK cultures were placed in one of the indicated treatment groups for 24 hours. Antimycin A (10 μM) was added at 21 hours following onset of experiment. The mean TER and fluorescein flux ± SE is reported from four independent experiments. ANOVA was performed followed by a Bonferroni post test with all comparisons against the cells in media containing 5% FBS and glucose, *P < 0.01.

From: Proinflammatory cytokines tumor necrosis factor-α and interferon-γ modulate epithelial barrier function in Madin-Darby canine kidney cells through mitogen activated protein kinase signaling