<p>Cells were exposed to LPS (1–100 ng/ml) in the presence and absence of serum for 24 hours. Conditioned media was then aspirated and TNFα, MCP-1 and IL-8 release measured by Luminex. Data expressed as mean ± SE (n = 6 subjects). **P<0.001, ***P<0.0002.</p
<p>(<b>A</b>) RAW 264.7 macrophages were stimulated with 10 ng/mL <i>E. coli</i> LPS in combination ...
<p>(A) ELISA quantification of IL-6 production in cell supernatants of NM and NP fibroblasts (n = 8 ...
<p>(A) DSCs were incubated for 12 hours with or without LPS (1 µg/mL) stimulation. After another 24-...
<p>Cells were exposed to MALP-2 (1–100 ng/ml) in the presence and absence of serum for 24 hours. Con...
<p>Cells were pre-incubated for 30 min with 10 µM of inhibitors of p38 (SB202190), JNK (SP600125) or...
<p>Cells were pre-incubated with an anti-CD14 or anti-MD2 neutralising antibody for 1 hr before expo...
<p>Alveolar macrophages (A) and ATII cells (B) were exposed to LPS (100 ng/ml) over a three hour tim...
<p><b>A</b>. IL-6 release was determined by ELISA in culture supernatants harvested 3 h, 6 h and 24 ...
<p>Using Simple PCI software analysis of images captured by confocal microscopy, the mean fluorescen...
Blood cells treated with endotoxin (LPS E. coli), DP-e or their combination. TNF-α (A), IL-8 (B) and...
<p>RAW 264.7 macrophages were exposed to 1 µg/mL of LPS, during 18 h and cell viability were assesse...
<p>The amount of TNFα, IL-6 and MCP1 was measured by ELISA from the whole blood plasma collected aft...
<p>Six-day cultured M-CSF MΦ were activated with IFNγ or with IL-4 to obtain M1 and M2 MΦ, respectiv...
<p>Blood samples were collected retro-bulbar from <i>Mrp4<sup>−/−</sup></i> mice (open bars) and <i>...
<p><b>A</b> 1×10<sup>5</sup> THP-1 cells, primary human monocytes, monocyte-derived DCs (moDCs), or ...
<p>(<b>A</b>) RAW 264.7 macrophages were stimulated with 10 ng/mL <i>E. coli</i> LPS in combination ...
<p>(A) ELISA quantification of IL-6 production in cell supernatants of NM and NP fibroblasts (n = 8 ...
<p>(A) DSCs were incubated for 12 hours with or without LPS (1 µg/mL) stimulation. After another 24-...
<p>Cells were exposed to MALP-2 (1–100 ng/ml) in the presence and absence of serum for 24 hours. Con...
<p>Cells were pre-incubated for 30 min with 10 µM of inhibitors of p38 (SB202190), JNK (SP600125) or...
<p>Cells were pre-incubated with an anti-CD14 or anti-MD2 neutralising antibody for 1 hr before expo...
<p>Alveolar macrophages (A) and ATII cells (B) were exposed to LPS (100 ng/ml) over a three hour tim...
<p><b>A</b>. IL-6 release was determined by ELISA in culture supernatants harvested 3 h, 6 h and 24 ...
<p>Using Simple PCI software analysis of images captured by confocal microscopy, the mean fluorescen...
Blood cells treated with endotoxin (LPS E. coli), DP-e or their combination. TNF-α (A), IL-8 (B) and...
<p>RAW 264.7 macrophages were exposed to 1 µg/mL of LPS, during 18 h and cell viability were assesse...
<p>The amount of TNFα, IL-6 and MCP1 was measured by ELISA from the whole blood plasma collected aft...
<p>Six-day cultured M-CSF MΦ were activated with IFNγ or with IL-4 to obtain M1 and M2 MΦ, respectiv...
<p>Blood samples were collected retro-bulbar from <i>Mrp4<sup>−/−</sup></i> mice (open bars) and <i>...
<p><b>A</b> 1×10<sup>5</sup> THP-1 cells, primary human monocytes, monocyte-derived DCs (moDCs), or ...
<p>(<b>A</b>) RAW 264.7 macrophages were stimulated with 10 ng/mL <i>E. coli</i> LPS in combination ...
<p>(A) ELISA quantification of IL-6 production in cell supernatants of NM and NP fibroblasts (n = 8 ...
<p>(A) DSCs were incubated for 12 hours with or without LPS (1 µg/mL) stimulation. After another 24-...