Role of the Scavenger Receptor CD36 in Accelerated Diabetic Atherosclerosis.
Miquel Navas-MadroñalEsmeralda CastelblancoMercedes CamachoMarta ConsegalAnna Ramirez-MorrosMaria Rosa SarriasPaulina PerezNuria AlonsoMaría GalánEsmeralda CastelblancoPublished in: International journal of molecular sciences (2020)
Diabetes mellitus entails increased atherosclerotic burden and medial arterial calcification, but the precise mechanisms are not fully elucidated. We aimed to investigate the implication of CD36 in inflammation and calcification processes orchestrated by vascular smooth muscle cells (VSMCs) under hyperglycemic and atherogenic conditions. We examined the expression of CD36, pro-inflammatory cytokines, endoplasmic reticulum (ER) stress markers, and mineralization-regulating enzymes by RT-PCR in human VSMCs, cultured in a medium containing normal (5 mM) or high glucose (22 mM) for 72 h with or without oxidized low-density lipoprotein (oxLDL) (24 h). The uptake of 1,1'-dioctadecyl-3,3,3',3-tetramethylindocarbocyanine perchlorate-fluorescently (DiI) labeled oxLDL was quantified by flow cytometry and fluorimetry and calcification assays were performed in VSMC cultured in osteogenic medium and stained by alizarin red. We observed induction in the expression of CD36, cytokines, calcification markers, and ER stress markers under high glucose that was exacerbated by oxLDL. These results were confirmed in carotid plaques from subjects with diabetes versus non-diabetic subjects. Accordingly, the uptake of DiI-labeled oxLDL was increased after exposure to high glucose. The silencing of CD36 reduced the induction of CD36 and the expression of calcification enzymes and mineralization of VSMC. Our results indicate that CD36 signaling is partially involved in hyperglycemia and oxLDL-induced vascular calcification in diabetes.
Keyphrases
- high glucose
- endothelial cells
- vascular smooth muscle cells
- type diabetes
- chronic kidney disease
- cardiovascular disease
- low density lipoprotein
- nk cells
- glycemic control
- endoplasmic reticulum
- flow cytometry
- mesenchymal stem cells
- angiotensin ii
- skeletal muscle
- risk factors
- anti inflammatory
- insulin resistance
- pet imaging
- induced pluripotent stem cells