Pigment epithelium-derived factor prevents endothelial dysfunction in early stage of hyperlipidemia by regulating
Haiping Wang1, Conghui Shen2, Yanfang Yang3
1Guangdong Engineering & Technology Research Center for Disease-Model Animals, Laboratory Animal Center, Sun Yat-sen University, Guangzhou, 510006, Guangdong, China; Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, Guangdong, China; Center of Prenatal Diagnosis, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, 510080, Guangdong, China.
Background And Aims:
Hyperlipidemia is typically characterized by lipid metabolism disorder. Pigment epithelium-derived factor (Pedf) is critical in the regulation of lipid metabolism. This study aimed to explore the expression patterns of Pedf during hyperlipidemia and its mechanism in regulating endothelial function.
Methods:
Pedf expression profiling were determined in both patients with hyperlipidemia and high-fat diet (HFD)-induced mice. Micro-CT, ultrasound biomicroscopy, and transmission electron microscopy (TEM) combined with molecular and biochemical analyses were performed on global Pedf knockout (Pedf-/-) mice and Pedf-/- mice injected with adeno-associated virus (AAV)-Pedf.
Results:
Pedf was upregulated in patients with hyperlipidemia and positively correlated with lipid levels, which was consistent with the findings in HFD-induced mouse models. The initial increase in Pedf is attributable to the activation of the NF-κB/TNFα signaling pathway during early-stage obesity. Conversely, prolonged HFD exposure led to a decrease in Pedf expression. Pedf-/- mice showed accelerated obesity progression, impaired endothelial function, heightened free fatty acid (FFA) uptake and exacerbated lipid deposition. Notably, reintroducing Pedf via AAV-Pedf delivery effectively restored endothelial function and mitigated lipid accumulation. TEM analysis revealed an increase in electron dense material between endothelial cells, and much more lipid droplets were observed in endothelial cells of Pedf-/- mice. Mechanistically, Pedf deficiency significantly activated the Apelin/Apj/VE-cadherin signaling pathway, leading to vascular remodeling, increased endothelial FFA uptake and endothelial dysfunction.
Conclusions:
Our findings suggest that Pedf exerts beneficial effect on the regulation of lipid metabolism and serves as a preventive agent against the progression of obesity and associated metabolic complications.
