<p>(A) The intracellular location of NF-κB p65 was determined in RAW264.7 cells by immunofluorescence using an anti-NF-κB p65 antibody with Alexa Fluor 555 labelling (red fluorescence), and the nuclei were counterstained with DAPI (blue fluorescence). (a) Untreated cells exhibit the localization of NF-κB in the cytoplasm. Cells stimulated with 100 ng/ml LPS (b) and 50 µM PAPS(c) display a significant increase in the translocation of NF-κB into the nucleus. (d) Stimulated cells in the presence of 50 µM PAPep maintained predominantly cytoplasmic NF-κB immunostaining, indicating inhibition of NF-κB translocation. Results are displayed individually or as merged images (confocal fluorescence microscopy). Data represent one of three experiments w...
<p>HK-2 cells were treated without or with 10 µM RGL for 2 hours and then stimulation with 1 μg/ml L...
<p>The 16HBE14o- cells were stimulated with vehicle control (A, B) and 100 µM UDP (C, D) for 60 min....
<p>(<b>A</b>) Nuclear translocation of p65/NF-κB subunit was assessed by immunofluorescence labeling...
<p>Macrophages were grown on glass coverslips for 24 hrs, and then stimulated with 100 ng/mL LPS. St...
<p>The LPS-stimulated THP-1 cells were treated with the N-terminal fragments of DYN 1–17 and U50,488...
<p>RAW264.7 macrophages were seeded in 8 well chamber slides at a density of 2×10<sup>4</sup> cells ...
<p>A: Cellular localization of p65 was analyzed by immunofluorescence staining. HaCaT cells were pre...
<p>(A) DU145 cells were pretreated with PMS1077 (50 µM) or TPCA-1(2 µM) for 6 h and followed by TNF-...
<p>FFAR4-GFP expressing LPS primed non-differentiated THP-1 cells were stimulated with ATP or nigeri...
<p>Cells were treated in the presence or absence of various concentrations (0–50 μg/ml) of AF for 30...
<p>A431 cells were treated with 20 µM LY294002 and 20 µM parthenolide for 1 h and followed by treati...
<p>A–B, RAW264.7 cells (A) and peritoneal macrophages (B) were stimulated with 100 ng/ml LPS in abse...
<p>Cells were fixed, permeabilised, stained with anti-NF-κB/p65 rabbit monoclonal antibody and visua...
<p>Kym-1 cells were stimulated with scTNF<sub>R2</sub> or TNC-scTNF<sub>R2</sub> (10 ng/ml) for 10, ...
<p>Human trophoblast-derived cells (JEG-3 cells) were pretreated with FA (40 μg/mL) for 1 h and then...
<p>HK-2 cells were treated without or with 10 µM RGL for 2 hours and then stimulation with 1 μg/ml L...
<p>The 16HBE14o- cells were stimulated with vehicle control (A, B) and 100 µM UDP (C, D) for 60 min....
<p>(<b>A</b>) Nuclear translocation of p65/NF-κB subunit was assessed by immunofluorescence labeling...
<p>Macrophages were grown on glass coverslips for 24 hrs, and then stimulated with 100 ng/mL LPS. St...
<p>The LPS-stimulated THP-1 cells were treated with the N-terminal fragments of DYN 1–17 and U50,488...
<p>RAW264.7 macrophages were seeded in 8 well chamber slides at a density of 2×10<sup>4</sup> cells ...
<p>A: Cellular localization of p65 was analyzed by immunofluorescence staining. HaCaT cells were pre...
<p>(A) DU145 cells were pretreated with PMS1077 (50 µM) or TPCA-1(2 µM) for 6 h and followed by TNF-...
<p>FFAR4-GFP expressing LPS primed non-differentiated THP-1 cells were stimulated with ATP or nigeri...
<p>Cells were treated in the presence or absence of various concentrations (0–50 μg/ml) of AF for 30...
<p>A431 cells were treated with 20 µM LY294002 and 20 µM parthenolide for 1 h and followed by treati...
<p>A–B, RAW264.7 cells (A) and peritoneal macrophages (B) were stimulated with 100 ng/ml LPS in abse...
<p>Cells were fixed, permeabilised, stained with anti-NF-κB/p65 rabbit monoclonal antibody and visua...
<p>Kym-1 cells were stimulated with scTNF<sub>R2</sub> or TNC-scTNF<sub>R2</sub> (10 ng/ml) for 10, ...
<p>Human trophoblast-derived cells (JEG-3 cells) were pretreated with FA (40 μg/mL) for 1 h and then...
<p>HK-2 cells were treated without or with 10 µM RGL for 2 hours and then stimulation with 1 μg/ml L...
<p>The 16HBE14o- cells were stimulated with vehicle control (A, B) and 100 µM UDP (C, D) for 60 min....
<p>(<b>A</b>) Nuclear translocation of p65/NF-κB subunit was assessed by immunofluorescence labeling...