Quercetin Mitigates Endothelial Activation in a Novel Intestinal-Endothelial-Monocyte/Macrophage Coculture Setup.
Hanne VissenaekensCharlotte GrootaertKatleen RaesJulie De MunckGuy SmaggheNico BoonJohn Van CampPublished in: Inflammation (2022)
Atherosclerosis initiation is associated with a pro-inflammatory state of the endothelium. Quercetin is a flavonoid abundantly present in plant-based foods, with a possible impact on cardiovascular health. In this study, the effects of quercetin on lipopolysaccharide (LPS)-mediated endothelial inflammation and monocyte adhesion and migration, which are initial steps of the atherogenic process, are studied. Novel in vitro multicellular models simulating the intestinal-endothelial-monocytes/macrophages axis allowed to combine relevant intestinal flavonoid absorption, metabolism and efflux, and the consequent bioactivity towards peripheral endothelial cells. In this triple coculture, quercetin exposure decreased monocyte adhesion to and macrophage migration through an LPS-stressed endothelium, and this was associated with significantly lower levels of soluble vascular cell adhesion molecule-1 (sVCAM-1). Furthermore, quercetin decreased the pro-inflammatory cell environment upon LPS-induced endothelial activation, in terms of tumor necrosis factor- α (TNF-α), interleukin-6 (IL-6), interleukin-8 (IL-8), and sVCAM-1 expression. These findings highlight a mode-of-action by which quercetin may positively impact the initial states of atherosclerosis under more physiologically relevant conditions in terms of quercetin concentrations, metabolites, and intercellular crosstalk.
Keyphrases
- endothelial cells
- lps induced
- inflammatory response
- cell adhesion
- high glucose
- dendritic cells
- rheumatoid arthritis
- nitric oxide
- cardiovascular disease
- adipose tissue
- oxidative stress
- vascular endothelial growth factor
- toll like receptor
- cystic fibrosis
- staphylococcus aureus
- anti inflammatory
- bone marrow
- long non coding rna
- cell migration
- solid state