<p>(A) Macrophages were treated for up to 5 h with 10 ng/ml LPS and RelA/p65 was assayed in the cytoplasm and nucleus. (B) Macrophages were primed for 3 h with LPS and then stimulated for different times. (B–C) The nuclear fractions were used for the assay of RelA/p65, c-Rel, and p50. (D) Binding of RelA/p65 and c-Rel, and histone H3 acetylation of the <i>ptgs2</i> promoter were assayed in the presence and absence of LPS priming 2 h after stimulation. These are representative experiments of at least two showing identical results.</p
<p>(<b>A</b>) The DNA-binding activity of NF-κB was analyzed by EMSA. Nuclear extracts were prepared...
<p>After incubation with Sch A and Sch B for 6 h, RAW264.7 macrophages were challenged with LPS (1 μ...
<p>(A-B), Peritoneal macrophages were isolated from LPS-challenged mice, recovered overnight and re-...
<p>(A) Macrophages were treated or not with compound <b>1</b> (25 μM) and stimulated with LPS (100 n...
<p>Macrophages were incubated with medium only, LPS, or LPS in the presence of BPs. (A) Expression o...
<p>(A) Cells were treated with 0.5, 5 and 15 μM 4'-HW for 1 h prior to stimulation with LPS (100 ng/...
<p>1×10<sup>6</sup> U937 monocytes were differentiated into macrophages with 100 nM PMA for 48 h. Ce...
<p>Mouse peritoneal macrophages were incubated with vehicle, Ber (2.0 µM), Ber (2.0 µM)+Y (5.0 µM) o...
<p>Non-transduced, mock shRNA transduced and gp96 shRNA transduced MM6 cells were treated with LPS (...
<p>Super-shift assays with anti-cRel, anti-RelA and anti-p50 antibodies using nuclear extract protei...
<p>(<b>A</b>) RAW 264.7 macrophages or (<b>B</b>) J774A.1 macrophages (both 5 × 10<sup>5</sup>/ml; 1...
<p>A) BMDMs were pulsed with medium alone or PL, LPS, PL+LPS. Extracts from BMDMs pulsed for mention...
<p>(A) BMMs were pretreated with DMSO or GSI for 1 and 4 hr and the cytosolic and nuclei fractions w...
<p><i>A</i> to <i>B</i>, Peritoneal macrophages were isolated from naïve or LPS-challenged, RT or he...
<p>Cells were stimulated with LPS (1 μg/mL) in the presence or absence of KLK peptide. After 30 min ...
<p>(<b>A</b>) The DNA-binding activity of NF-κB was analyzed by EMSA. Nuclear extracts were prepared...
<p>After incubation with Sch A and Sch B for 6 h, RAW264.7 macrophages were challenged with LPS (1 μ...
<p>(A-B), Peritoneal macrophages were isolated from LPS-challenged mice, recovered overnight and re-...
<p>(A) Macrophages were treated or not with compound <b>1</b> (25 μM) and stimulated with LPS (100 n...
<p>Macrophages were incubated with medium only, LPS, or LPS in the presence of BPs. (A) Expression o...
<p>(A) Cells were treated with 0.5, 5 and 15 μM 4'-HW for 1 h prior to stimulation with LPS (100 ng/...
<p>1×10<sup>6</sup> U937 monocytes were differentiated into macrophages with 100 nM PMA for 48 h. Ce...
<p>Mouse peritoneal macrophages were incubated with vehicle, Ber (2.0 µM), Ber (2.0 µM)+Y (5.0 µM) o...
<p>Non-transduced, mock shRNA transduced and gp96 shRNA transduced MM6 cells were treated with LPS (...
<p>Super-shift assays with anti-cRel, anti-RelA and anti-p50 antibodies using nuclear extract protei...
<p>(<b>A</b>) RAW 264.7 macrophages or (<b>B</b>) J774A.1 macrophages (both 5 × 10<sup>5</sup>/ml; 1...
<p>A) BMDMs were pulsed with medium alone or PL, LPS, PL+LPS. Extracts from BMDMs pulsed for mention...
<p>(A) BMMs were pretreated with DMSO or GSI for 1 and 4 hr and the cytosolic and nuclei fractions w...
<p><i>A</i> to <i>B</i>, Peritoneal macrophages were isolated from naïve or LPS-challenged, RT or he...
<p>Cells were stimulated with LPS (1 μg/mL) in the presence or absence of KLK peptide. After 30 min ...
<p>(<b>A</b>) The DNA-binding activity of NF-κB was analyzed by EMSA. Nuclear extracts were prepared...
<p>After incubation with Sch A and Sch B for 6 h, RAW264.7 macrophages were challenged with LPS (1 μ...
<p>(A-B), Peritoneal macrophages were isolated from LPS-challenged mice, recovered overnight and re-...