Fig. 4.
Fig. 4. Inhibition of cell adhesion molecule expression by ritonavir. / Flow cytometry (FACS) histograms of adhesion molecule expression were obtained from endothelial cells (HUVECs) that were treated in cultures (about 80% confluent) with TNF-α (5 ng/mL) or with TNF-α and ritonavir (20 μmol/L) for 4 hours. Aliquots of detached cells were stained with PE-conjugated antibodies for VCAM-1 (A), ICAM-1 (B), and E-selectin (C), as well as isotype-matched controls. Expression of adhesion molecules on TNF-α– and ritonavir-treated cells (solid line) was compared with TNF-α–stimulated cells (dotted line) and untreated cells (dashed line) as depicted in histogram overlays. Two independent experiments with similar results were performed.

Inhibition of cell adhesion molecule expression by ritonavir.

Flow cytometry (FACS) histograms of adhesion molecule expression were obtained from endothelial cells (HUVECs) that were treated in cultures (about 80% confluent) with TNF-α (5 ng/mL) or with TNF-α and ritonavir (20 μmol/L) for 4 hours. Aliquots of detached cells were stained with PE-conjugated antibodies for VCAM-1 (A), ICAM-1 (B), and E-selectin (C), as well as isotype-matched controls. Expression of adhesion molecules on TNF-α– and ritonavir-treated cells (solid line) was compared with TNF-α–stimulated cells (dotted line) and untreated cells (dashed line) as depicted in histogram overlays. Two independent experiments with similar results were performed.

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