<p>The cells were treated with increasing concentrations of BJe (0.05–0.5 mg/ml for 30 min) prior to add LPS (500 ng/ml; 3 hs). Then, secretion of IL-6 (A), IL-1β (B) and TNF-α (C) in the media was evaluated by ELISA assay. Data are the mean ± SEM of three independent experiments performed in triplicate. *** p<0.001, significant differences <i>vs</i> untreated cultures; <sup>§</sup> p<0.05 and <sup>§§§</sup> p<0.001, significant differences <i>vs</i> LPS treated cells (ANOVA followed by Student-Newman Keuls multiple comparisons test).</p
<p>(A) Cells were treated with different concentrations of LPS for 24 h. Secretion of TNF-α in cultu...
<p>Control and SPR210<sub>L</sub>(DN) cells were plated in 12-well tissue culture dishes at a densit...
<p>(<b>A</b>) J774A.1 macrophages, (<b>B</b>) peritoneal macrophages, or (<b>C</b>) JAWSII dendritic...
<p>THP-1 cells were treated with different concentrations of BJe (0.05–0.5 mg/ml for 30 min) before ...
<p>Different concentrations of BJe (0.01, 0.05, 0.1 and 0.5 mg/ml) were added to the culture medium ...
<p>(A) The cells were exposed to 0.1 mg/ml BJe 30 min before LPS treatment (500 ng/ml for 3 hs), and...
<p>(A) After LPS treatment in presence or absence of BJe and/or Sirtinol, THP-1 cells were lysed and...
<p><b>A</b>. IL-6 release was determined by ELISA in culture supernatants harvested 3 h, 6 h and 24 ...
<p><b>A</b> 1×10<sup>5</sup> THP-1 cells, primary human monocytes, monocyte-derived DCs (moDCs), or ...
<p>BM and SCM were activated with LPS to measure the difference in their pro-inflammatory molecules ...
<p>A, B. Effects of stimulating THP-1 cells with a combination of LPS and sCD26/DPPIV(+) or sCD26/DP...
<p>ARPE19 cells were treated with two concentrations of LPS (20 and 50 µg/ml) for 24 hr and the mRNA...
<p><b>A.</b> Simultaneous activation of monocytes with LPS and LILRA2 cross-linking for 18 h signifi...
<p>The addition of LPS to BV-2 microglial cell cultures resulted in a significant increase in IL-6, ...
<p>(A) ELISA quantification of IL-6 production in cell supernatants of NM and NP fibroblasts (n = 8 ...
<p>(A) Cells were treated with different concentrations of LPS for 24 h. Secretion of TNF-α in cultu...
<p>Control and SPR210<sub>L</sub>(DN) cells were plated in 12-well tissue culture dishes at a densit...
<p>(<b>A</b>) J774A.1 macrophages, (<b>B</b>) peritoneal macrophages, or (<b>C</b>) JAWSII dendritic...
<p>THP-1 cells were treated with different concentrations of BJe (0.05–0.5 mg/ml for 30 min) before ...
<p>Different concentrations of BJe (0.01, 0.05, 0.1 and 0.5 mg/ml) were added to the culture medium ...
<p>(A) The cells were exposed to 0.1 mg/ml BJe 30 min before LPS treatment (500 ng/ml for 3 hs), and...
<p>(A) After LPS treatment in presence or absence of BJe and/or Sirtinol, THP-1 cells were lysed and...
<p><b>A</b>. IL-6 release was determined by ELISA in culture supernatants harvested 3 h, 6 h and 24 ...
<p><b>A</b> 1×10<sup>5</sup> THP-1 cells, primary human monocytes, monocyte-derived DCs (moDCs), or ...
<p>BM and SCM were activated with LPS to measure the difference in their pro-inflammatory molecules ...
<p>A, B. Effects of stimulating THP-1 cells with a combination of LPS and sCD26/DPPIV(+) or sCD26/DP...
<p>ARPE19 cells were treated with two concentrations of LPS (20 and 50 µg/ml) for 24 hr and the mRNA...
<p><b>A.</b> Simultaneous activation of monocytes with LPS and LILRA2 cross-linking for 18 h signifi...
<p>The addition of LPS to BV-2 microglial cell cultures resulted in a significant increase in IL-6, ...
<p>(A) ELISA quantification of IL-6 production in cell supernatants of NM and NP fibroblasts (n = 8 ...
<p>(A) Cells were treated with different concentrations of LPS for 24 h. Secretion of TNF-α in cultu...
<p>Control and SPR210<sub>L</sub>(DN) cells were plated in 12-well tissue culture dishes at a densit...
<p>(<b>A</b>) J774A.1 macrophages, (<b>B</b>) peritoneal macrophages, or (<b>C</b>) JAWSII dendritic...