<p>The RAW264.7 cells were seeded in a 24-well plate, treated with 400 or 800 µg/ml AEGT for 1 h and stimulated with 1 µg/ml LPS for 24 h. The cell lysates were collected, and p38, JNK, and ERK1/2 phosphorylation was analyzed by western blot analysis with specific antibodies. The relative value of the LPS- group or AEGT/LPS-treated group over the untreated group was measured by densitometry following normalization to cellular GAPDH levels. The basal level of promoter activity in the AEGT/LPS-untreated cells was defined as 1. Error bars indicate the means ± SD of three independent experiments. *<i>P</i><0.05; **<i>P</i><0.01.</p
<p>Control and AE-BCT-pre-treated HT1080 cells were stimulated with 5 nM PMA for the indicated perio...
<p>ARPE19 cells were treated with two concentrations of LPS (20 and 50 µg/ml) for 24 hr and the mRNA...
<p>AGS cells were grown in 100-mm plates and infected with either Ad-LacZ or Ad-PKG II. Then, the ce...
<p>(A) The RAW264.7 cells were seeded in a 24-well plate, and treated with 400 or 800 µg/ml AEGT for...
<p>Cells were seeded in a 24-well plate treated with 400 or 800 µg/ml AEGT for 1 h, and then incubat...
<p>Immunoblot analyses of phosphorylated IKK, IκBα and phosphorylated- and total-p65. The experiment...
<p>Cells were seeded in a 96-well plate and treated with 400 or 800 µg/ml AEGT for 1 h, and then inc...
<p>Cells were treated for 180(control), LPS (100 ng/ml) alone, or LPS combined with 20 µM of the p38...
<p>p44/42 ERK (<b>A1–A3</b>) and p38 MAPK (<b>B1–B3</b>) were phosphorylated after CXCL12 (20 nM) st...
<p>AGS cells were infected with Ad-LacZ or Ad-PKG II for 48 h and serum starved o/n. In Ad-LacZ+EGF ...
<p>(A) Cells were treated with different concentrations of LPS for 24 h. Secretion of TNF-α in cultu...
<p>AGS cells were treated same as described in <a href="http://www.plosone.org/article/info:doi/10.1...
<p>AGS cells were treated same as described in <a href="http://www.plosone.org/article/info:doi/10.1...
<p>Cells overexpressing LPA<sub>1</sub> (panels A and D), LPA<sub>2</sub> (panels B and E) or LPA<su...
<p>BV2 cells were treated with TET at working concentrations for 2 h.Then, LPS was added to each pla...
<p>Control and AE-BCT-pre-treated HT1080 cells were stimulated with 5 nM PMA for the indicated perio...
<p>ARPE19 cells were treated with two concentrations of LPS (20 and 50 µg/ml) for 24 hr and the mRNA...
<p>AGS cells were grown in 100-mm plates and infected with either Ad-LacZ or Ad-PKG II. Then, the ce...
<p>(A) The RAW264.7 cells were seeded in a 24-well plate, and treated with 400 or 800 µg/ml AEGT for...
<p>Cells were seeded in a 24-well plate treated with 400 or 800 µg/ml AEGT for 1 h, and then incubat...
<p>Immunoblot analyses of phosphorylated IKK, IκBα and phosphorylated- and total-p65. The experiment...
<p>Cells were seeded in a 96-well plate and treated with 400 or 800 µg/ml AEGT for 1 h, and then inc...
<p>Cells were treated for 180(control), LPS (100 ng/ml) alone, or LPS combined with 20 µM of the p38...
<p>p44/42 ERK (<b>A1–A3</b>) and p38 MAPK (<b>B1–B3</b>) were phosphorylated after CXCL12 (20 nM) st...
<p>AGS cells were infected with Ad-LacZ or Ad-PKG II for 48 h and serum starved o/n. In Ad-LacZ+EGF ...
<p>(A) Cells were treated with different concentrations of LPS for 24 h. Secretion of TNF-α in cultu...
<p>AGS cells were treated same as described in <a href="http://www.plosone.org/article/info:doi/10.1...
<p>AGS cells were treated same as described in <a href="http://www.plosone.org/article/info:doi/10.1...
<p>Cells overexpressing LPA<sub>1</sub> (panels A and D), LPA<sub>2</sub> (panels B and E) or LPA<su...
<p>BV2 cells were treated with TET at working concentrations for 2 h.Then, LPS was added to each pla...
<p>Control and AE-BCT-pre-treated HT1080 cells were stimulated with 5 nM PMA for the indicated perio...
<p>ARPE19 cells were treated with two concentrations of LPS (20 and 50 µg/ml) for 24 hr and the mRNA...
<p>AGS cells were grown in 100-mm plates and infected with either Ad-LacZ or Ad-PKG II. Then, the ce...