<p>PBMCs were isolated from fresh donor blood buffy coats. After an aggregation step, the cells were cultured with or without 25 ng/ml IL-4 and 50 ng/ml GM-CSF for 5 days to derive MDDC or monocytes, respectively. Expression of several cell surface markers was analyzed flow cytometrically with specific PE-labeled mAbs. Data represent mean % positive cells ± standard error of the mean (SEM) from 5 different donors. The expression level of each marker was compared between monocytes and MDDC and the corresponding p-value was calculated with a paired <i>t</i>-test.</p
<p>Histogram plots show surface marker staining as hatched areas and isotype controls as black lines...
<p>The percentage of iNKT cells in PBMC (A) and in monocytes (B) was analyzed by flow cytometry with...
<p>A) Time-course analysis of cell surfaces marker expressed during monocytopoiesis. Adherent EBs we...
<p>PBMC were stained with mouse monoclonal antibodies and then analyzed by flow cytometry. Monocytes...
<p>Monocytes were cultured under indicated conditions for 7 days. (A) Expression of CD80, CD86, F4/8...
<p>Primary monocytes and AEC were enriched from naïve donor mice and co-cultured for three, six or t...
<p>a) PBMCs co-stained for PD-1H along with Monocytes (CD14), T cell (CD3), and B cell (CD19) marker...
*<p>Monocytes cultured during 3 days with GMCSF and autologous plasma but without IFN.</p>**<p>n = 5...
<p>PBMCs were differentiated using 10 ng/mL granulocyte-macrophage colony stimulating factor (GM-CSF...
<p>(A) Shown are isotype control dot plots and CD14 and CD16 expression in freshly obtained and cryo...
<p>Monocytes were cultured in RPMI medium, RLEC-CM or hNPC-CM with the indicated cytokine combinatio...
<p>Frh-imdDCs (black), crp-imdDCs (blue) and isotype-matched controls (red) were analyzed for the ex...
<p>Monocytes were negatively selected from PBMC using magnetic beads. Immature moDC were generated w...
<p>Monocytes were differentiated during 5 days in complete RPMI medium containing 40 ng/mL GM- CSF a...
The round THP-1 cells changed to be adherent flatten cells (white arrows). Under forward scatter and...
<p>Histogram plots show surface marker staining as hatched areas and isotype controls as black lines...
<p>The percentage of iNKT cells in PBMC (A) and in monocytes (B) was analyzed by flow cytometry with...
<p>A) Time-course analysis of cell surfaces marker expressed during monocytopoiesis. Adherent EBs we...
<p>PBMC were stained with mouse monoclonal antibodies and then analyzed by flow cytometry. Monocytes...
<p>Monocytes were cultured under indicated conditions for 7 days. (A) Expression of CD80, CD86, F4/8...
<p>Primary monocytes and AEC were enriched from naïve donor mice and co-cultured for three, six or t...
<p>a) PBMCs co-stained for PD-1H along with Monocytes (CD14), T cell (CD3), and B cell (CD19) marker...
*<p>Monocytes cultured during 3 days with GMCSF and autologous plasma but without IFN.</p>**<p>n = 5...
<p>PBMCs were differentiated using 10 ng/mL granulocyte-macrophage colony stimulating factor (GM-CSF...
<p>(A) Shown are isotype control dot plots and CD14 and CD16 expression in freshly obtained and cryo...
<p>Monocytes were cultured in RPMI medium, RLEC-CM or hNPC-CM with the indicated cytokine combinatio...
<p>Frh-imdDCs (black), crp-imdDCs (blue) and isotype-matched controls (red) were analyzed for the ex...
<p>Monocytes were negatively selected from PBMC using magnetic beads. Immature moDC were generated w...
<p>Monocytes were differentiated during 5 days in complete RPMI medium containing 40 ng/mL GM- CSF a...
The round THP-1 cells changed to be adherent flatten cells (white arrows). Under forward scatter and...
<p>Histogram plots show surface marker staining as hatched areas and isotype controls as black lines...
<p>The percentage of iNKT cells in PBMC (A) and in monocytes (B) was analyzed by flow cytometry with...
<p>A) Time-course analysis of cell surfaces marker expressed during monocytopoiesis. Adherent EBs we...