Palmitic acid in type 2 diabetes mellitus promotes atherosclerotic plaque vulnerability via macrophage Dll4 signaling.
Xiqiang WangLing ZhuJing LiuYanpeng MaChuan QiuChengfeng LiuYangchao GongYa YuwenGongchang GuanYong ZhangShuo PanJunkui WangZhongwei LiuPublished in: Nature communications (2024)
Patients with Type 2 Diabetes Mellitus are increasingly susceptible to atherosclerotic plaque vulnerability, leading to severe cardiovascular events. In this study, we demonstrate that elevated serum levels of palmitic acid, a type of saturated fatty acid, are significantly linked to this enhanced vulnerability in patients with Type 2 Diabetes Mellitus. Through a combination of human cohort studies and animal models, our research identifies a key mechanistic pathway: palmitic acid induces macrophage Delta-like ligand 4 signaling, which in turn triggers senescence in vascular smooth muscle cells. This process is critical for plaque instability due to reduced collagen synthesis and deposition. Importantly, our findings reveal that macrophage-specific knockout of Delta-like ligand 4 in atherosclerotic mice leads to reduced plaque burden and improved stability, highlighting the potential of targeting this pathway. These insights offer a promising direction for developing therapeutic strategies to mitigate cardiovascular risks in patients with Type 2 Diabetes Mellitus.
Keyphrases
- cardiovascular disease
- cardiovascular events
- coronary artery disease
- vascular smooth muscle cells
- climate change
- endothelial cells
- adipose tissue
- end stage renal disease
- fatty acid
- genome wide
- chronic kidney disease
- newly diagnosed
- ejection fraction
- human health
- prognostic factors
- sensitive detection
- cancer therapy
- early onset
- single cell
- dna methylation
- insulin resistance
- metabolic syndrome
- drug delivery
- skeletal muscle