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Logo of acbAnatomy & Cell BiologyAboutFor Contributorse-SubmissionThis article
 
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Published online Dec 30, 2011. doi: 10.5115/acb.2011.44.4.265
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Fig. 1
Laminar flow inhibits 15d-PGJ2-induced endothelial apoptosis. Confluent HUVECs were cultured under L-flow (12 dyne/cm2) or a static condition for 24 h. Cells were then exposed to 10 µM 15d-PGJ2 for 8 h. (A) Cell lysates were applied for immunoblotting with anti-PARP, anti-cleaved caspase 3, and anti-tubulin antibodies. Data are representative of results from three separate experiments. (B) Cell viability was determined by using MTT assay. Data are expressed as the mean±SD from three independent experiments. *P<0.01. Morphological changes of HUVECs were examined by microscopy under control (C), 15d-PGJ2 (D), or 15d-PGJ2 under L-flow (E). Scale bars=100 µm (C-E). 15d-PGJ2, 15-deoxy-Δ(12,14)-prostaglandin J2; HUVECs, human umbilical vein endothelial cells; L-flow, steady laminar flow; PARP, poly (ADP-ribose) polymerase; OD, optical density.
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