The State Key Laboratory of Medical Genomics, Shanghai Key Laboratory of Hypertension, Department of Hypertension, Ruijin Hospital and Shanghai Institute of Hypertension, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
The State Key Laboratory of Medical Genomics, Shanghai Key Laboratory of Hypertension, Department of Hypertension, Ruijin Hospital and Shanghai Institute of Hypertension, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China
Diabetes. 2018 Aug;67(8):1549-1560. doi: 10.2337/db18-0098. Epub 2018 May 24.
Obesity increases the risk of vascular diseases, including aortic aneurysm (AA). Perivascular adipose tissue (PVAT) surrounding arteries are altered during obesity. However, the underlying mechanism of adipose tissue, especially PVAT, in the pathogenesis of AA is still unclear. Here we showed that angiotensin II (AngII) infusion increases the incidence of AA in leptin-deficient obese mice (/) and high-fat diet-induced obese mice with adventitial inflammation. Furthermore, transcriptome analysis revealed that platelet-derived growth factor-D (PDGF-D) was highly expressed in the PVAT of / mice. Therefore, we hypothesized that PDGF-D mediates adventitial inflammation, which provides a direct link between PVAT dysfunction and AA formation in AngII-infused obese mice. We found that PDGF-D promotes the proliferation, migration, and inflammatory factors expression in cultured adventitial fibroblasts. In addition, the inhibition of PDGF-D function significantly reduced the incidence of AA in AngII-infused obese mice. More importantly, adipocyte-specific PDGF-D transgenic mice are more susceptible to AA formation after AngII infusion accompanied by exaggerated adventitial inflammatory and fibrotic responses. Collectively, our findings reveal a notable role of PDGF-D in the AA formation during obesity, and modulation of this cytokine might be an exploitable treatment strategy for the condition.
肥胖增加了血管疾病的风险,包括主动脉瘤(AA)。动脉周围的血管周围脂肪组织(PVAT)在肥胖期间发生改变。然而,脂肪组织,特别是 PVAT,在 AA 发病机制中的潜在机制仍不清楚。在这里,我们发现血管紧张素 II(AngII)输注增加了瘦素缺乏肥胖小鼠(/)和具有外膜炎症的高脂肪饮食诱导肥胖小鼠中 AA 的发生率。此外,转录组分析显示,血小板衍生生长因子-D(PDGF-D)在 / 小鼠的 PVAT 中高度表达。因此,我们假设 PDGF-D 介导外膜炎症,这为肥胖小鼠 AngII 输注中 PVAT 功能障碍与 AA 形成之间提供了直接联系。我们发现 PDGF-D 促进培养的外膜成纤维细胞的增殖、迁移和炎症因子表达。此外,PDGF-D 功能的抑制显著降低了 AngII 输注肥胖小鼠中 AA 的发生率。更重要的是,脂肪细胞特异性 PDGF-D 转基因小鼠在 AngII 输注后更容易形成 AA,并伴有外膜炎症和纤维化反应的夸大。总之,我们的研究结果揭示了 PDGF-D 在肥胖期间 AA 形成中的显著作用,调节这种细胞因子可能是一种可行的治疗策略。