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. 2012 Jun 13;303(5):F632–F638. doi: 10.1152/ajprenal.00169.2012

Fig. 1.

Fig. 1.

Fluid shear stress (FSS) induces prostaglandin E2 (PGE2) secretion into the media bathing cultured inner medullary collecting duct type 3 (IMCD3; A) and mpk cortical collecting duct (mpkCCD; B) cells and this response in IMCD3 cells is inhibited equally by cyclooxygenase (COX)-1 or COX-2 inhibitors (C). IMCD3 and mpkCCD cells were grown to confluence and exposed to 0.4 dyn/cm2 of FSS or maintained under static condition for 2 h. Cells were incubated in culture media for 1 h, the conditioned media were collected, and PGE2 concentrations (pg/ml) were measured by enzyme immunoassay. The PGE2 concentration was normalized to the amount of cellular protein (pg·ml−1·μg−1) present on the slide. Sheared IMCD3 (A) and mpkCCD (B) cells released more PGE2 than their respective static controls. Inhibitors of COX-1 (100 nM SC560) or COX-2 (1 μM CAY10404) reduced FSS-induced PGE2 release by 62.0 ± 8.4% (*P < 0.05) and 70.0 ± 2.7% (*P < 0.05) compared with the shear-untreated IMCD3 cells, respectively (C). PGE2 concentration remained greater than static control (#P < 0.05).