Journal: iScience
Article Title: Deciphering the role of endothelial granulocyte macrophage-CSF in chronic inflammation associated with HIV
doi: 10.1016/j.isci.2024.110909
Figure Lengend Snippet: Modulation of LPS-induced GM-CSF expression by human aortic endothelial cells (EC) through pharmacological interventions Endothelial cells were cultured in medium alone or medium supplemented with LPS (100 ng/mL), LPS + Dapa (1μg/mL) or LPS + TLR-4 Inhibitor (TLR4-C34) (10μg/mL). (A) Representative microscopy and fluorescent images of NBD glucose uptake under the indicated conditions (left) and violin plots show the quantification of NBD glucose uptake (MFI, right) in EC receiving indicated treatments (data from one of the 3 independent experiments, each circle represents MFI value from one EC, n = ∼100 cells/experiment, ∗∗∗ p < 0.0005). (B) Immunofluorescence microscopy images (left) and violin plots showing quantified image data (MFI/DAPI ratio, right) illustrating KLF2 protein expression in indicated treatment groups (data from 100 ECs per condition; each circle represents average MFI values from one image with 5–10 ECs). (C) ELISA data illustrate GM-CSF protein concentrations in supernatants of endothelial cell cultures after 24 h of incubation under specified conditions ( n = 3; ∗ p < 0.05). (D) Violin plots show ELISA data of GM-CSF levels in plasma samples from PWH, with ( n = 7) and without ( n = 10) receiving Dapa treatment (∗∗∗ p < 0.0005). All data are represented as mean ± SEM.
Article Snippet: TLR-4 Inhibitor (TLR4-C34) (1μg/mL) , Cayman Chemical Co. , #18514.
Techniques: Expressing, Cell Culture, Microscopy, Immunofluorescence, Enzyme-linked Immunosorbent Assay, Incubation, Clinical Proteomics