(A) U373 cells were stimulated with 10 ng/ml IL-1 or 5 μM S1P for the indicated times. The cell lysates were prepared, and analyzed by Western blotting with anti-phospho-ERK, anti-phospho-JNK, anti-IkBα, anti-ERK. Blots were stripped and re-probed with anti-tubulin antibodies to insure equal loading and transfer. (B, C) U373 cells were pretreated with 1 μM U0126, 10 μM LY294002, 1 μM SP600125, 10 μM SB202190, 5 μM Go6983, or 5 μM Y27632 for 1 hour, and subsequently stimulated with 5 μM S1P for 18 hours. RNA was isolated, and the expression of PAI-1 (B) and uPAR (C) was analyzed by qPCR. The data were normalized to GAPDH mRNA, and expressed as a ratio to mRNA levels in untreated cells. Asterisks indicate statistically significant inhibition. (D) U373-TAM67 cells were preincubated with 1μg/ml of tetracycline for 24 hours, and then stimulated with 10 ng/ml IL-1 or 5 μM S1P for 18 hours, RNA was isolated and analyzed as in (B, C).