<p><b>(A)</b> THP-1 monocytes and THP-1 MDM; <b>(B)</b> healthy peripheral blood monocytes and corresponding MDM <b>(C)</b> synovial fluid monocytes and corresponding MDM. Results are expressed as fold change mRNA expression (compared to <i>18s</i> RNA). Each experiment was run in triplicate, with data expressed as mean ± SEM of five independent experiments. Relative <i>TSPO</i> mRNA expression in MDM was compared to their respective monocyte counterpart whereby statistically significant differences are noted as **p<0.001 using Student’s <i>t</i>-test.</p
<p>Human monocytes were either unexposed (Mon) or exposed to CMFDA-labeled three different cancer ce...
<p>THP-1 monocytes were treated for 8 hours with RPMI-1640 medium (control 1–6) or CSE (1–6). RNA wa...
<p><b>Copyright information:</b></p><p>Taken from "Expression of inflammatory host genes in -infecte...
<p>(i) representative Western blots of TSPO protein with β-actin acting as loading control and (ii) ...
mRNA gene expression was measured by RT-qPCR and presented as relative fold change of the non-treate...
<p>RT-qPCR of mRNA of TNF-α (A) and IL-1β (B). Kinetic studies of mRNA-response (C and D). Isolated ...
<p>RNA was extracted from resting (open bars) or stimulated (black bars) monocytes (A) and their ind...
<p>RT-qPCR of mRNA of inflammasome member NALP3 (A) and caspase 1 (B). Arbitrary units. Isolated mon...
<p>THP-1 cells were cultured in complete media in the absence or presence of 100 nM 1,25-D3 (added a...
Percentage expression of CD14+CD16− monocytes (A), CD14+CD16+ monocytes (B) and CD14dimCD16+ monocyt...
<p>Quantitative RT-PCR (qRT-PCR) for CD100 (A) or STAT-1 (B) in PB monocytes, macrophages and foam c...
<p>Human peripheral-blood monocytes are used as an established in vitro system for generating macrop...
<p>(A–C) WT and <i>Nod2</i>-/- mice (n = 3/group) were infected or not in. with IAV (50 pfu) and tre...
<p><i>Relative mRNA expression of DUOX1, PRDX2, GPX3, SOD2 and GPX7 in monocytes and moDCs</i>. mRNA...
<p>THP-1 monocytes were treated for 8 hours with RPMI-1640 medium (control 1–6) or CSE (1–6). RNA wa...
<p>Human monocytes were either unexposed (Mon) or exposed to CMFDA-labeled three different cancer ce...
<p>THP-1 monocytes were treated for 8 hours with RPMI-1640 medium (control 1–6) or CSE (1–6). RNA wa...
<p><b>Copyright information:</b></p><p>Taken from "Expression of inflammatory host genes in -infecte...
<p>(i) representative Western blots of TSPO protein with β-actin acting as loading control and (ii) ...
mRNA gene expression was measured by RT-qPCR and presented as relative fold change of the non-treate...
<p>RT-qPCR of mRNA of TNF-α (A) and IL-1β (B). Kinetic studies of mRNA-response (C and D). Isolated ...
<p>RNA was extracted from resting (open bars) or stimulated (black bars) monocytes (A) and their ind...
<p>RT-qPCR of mRNA of inflammasome member NALP3 (A) and caspase 1 (B). Arbitrary units. Isolated mon...
<p>THP-1 cells were cultured in complete media in the absence or presence of 100 nM 1,25-D3 (added a...
Percentage expression of CD14+CD16− monocytes (A), CD14+CD16+ monocytes (B) and CD14dimCD16+ monocyt...
<p>Quantitative RT-PCR (qRT-PCR) for CD100 (A) or STAT-1 (B) in PB monocytes, macrophages and foam c...
<p>Human peripheral-blood monocytes are used as an established in vitro system for generating macrop...
<p>(A–C) WT and <i>Nod2</i>-/- mice (n = 3/group) were infected or not in. with IAV (50 pfu) and tre...
<p><i>Relative mRNA expression of DUOX1, PRDX2, GPX3, SOD2 and GPX7 in monocytes and moDCs</i>. mRNA...
<p>THP-1 monocytes were treated for 8 hours with RPMI-1640 medium (control 1–6) or CSE (1–6). RNA wa...
<p>Human monocytes were either unexposed (Mon) or exposed to CMFDA-labeled three different cancer ce...
<p>THP-1 monocytes were treated for 8 hours with RPMI-1640 medium (control 1–6) or CSE (1–6). RNA wa...
<p><b>Copyright information:</b></p><p>Taken from "Expression of inflammatory host genes in -infecte...