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外膜成纤维细胞衍生的血管内皮生长因子促进血管壁相关新生内膜形成和巨噬细胞募集。

Adventitial fibroblast-derived vascular endothelial growth factor promotes vasa vasorum-associated neointima formation and macrophage recruitment.

机构信息

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, 197 Ruijin 2nd Road, Shanghai 200025, China.

Department of Hypertension, Ruijin Hospital North, Shanghai Jiao Tong University School of Medicine, 999 Xiwang Road, Shanghai 201801, China.

出版信息

Cardiovasc Res. 2020 Mar 1;116(3):708-720. doi: 10.1093/cvr/cvz159.

Abstract

AIMS

Adventitial vasa vasorum provides oxygen and nourishment to the vascular wall, but whether it regulates vascular disease remains unclear. We have previously shown that an increased expression of VEGF (vascular endothelial growth factor) is associated with macrophage infiltration. This study aims to determine whether adventitial fibroblast (AF)-derived VEGF increases the number of vasa vasorum contributing to neointima formation through macrophage recruitment.

METHODS AND RESULTS

In rat balloon injury model, vasa vasorum count was increased particularly in the adventitia accompanied by cell proliferation and VEGF expression. Both endogenous and PKH26-labelled exogenous macrophages were mainly distributed in adventitia around vasa vasorum. Interestingly, perivascular delivery of Ranibizumab preferentially concentrated in adventitia resulted in a decrease of neointima formation with concurrent reduction of vasa vasorum count and macrophage infiltration. AFs with adenovirus-mediated VEGF over-expression delivered to the adventitia significantly enhanced these pathological changes after injury. In Tie2-cre/Rosa-LoxP-RFP mice, endothelial cells were increased in the adventitia after wire injury. By using multiphoton laser scanning microscopy, macrophage rolling, adhesion and transmigration were observed in vasa vasorum. Moreover, adoptive transfer of macrophages accelerated injury-induced neointima formation. VEGF-neutralizing antibody administration also attenuated wire injury-induced neointima formation and macrophage infiltration. In primary cultured AFs, exogenous VEGF increased VEGF expression and secretion in a time- and dose-dependent manner. AF-conditioned medium promoted endothelial cell angiogenesis, vascular cell adhesion molecule-1 expression and macrophage adhesion was blocked by VEGF-neutralizing antibody and VEGFR2 inhibitor ZM323881, which also inhibited activation of VEGFR2/ERK1/2 pathway.

CONCLUSION

These results demonstrate that AF-derived VEGF plays a significant role in the increase of vasa vasorum count which is involved in macrophage recruitment and neointima formation.

摘要

目的

血管外膜的血管腔提供氧气和营养物质给血管壁,但它是否调节血管疾病尚不清楚。我们之前已经表明,血管内皮生长因子(VEGF)的表达增加与巨噬细胞浸润有关。本研究旨在确定外膜成纤维细胞(AF)衍生的 VEGF 是否通过招募巨噬细胞增加有助于新生内膜形成的血管腔数量。

方法和结果

在大鼠球囊损伤模型中,血管腔数量增加,特别是在外膜中,伴随着细胞增殖和 VEGF 表达。内源性和 PKH26 标记的外源性巨噬细胞主要分布在血管腔周围的外膜中。有趣的是,雷珠单抗的血管周围给药主要集中在外膜,导致新生内膜形成减少,同时血管腔数量和巨噬细胞浸润减少。将腺病毒介导的 VEGF 过表达转染到外膜中,在损伤后显著增强了这些病理变化。在 Tie2-cre/Rosa-LoxP-RFP 小鼠中,血管损伤后内皮细胞在外膜中增加。通过多光子激光扫描显微镜观察到巨噬细胞在血管腔中的滚动、黏附和迁移。此外,巨噬细胞的过继转移加速了损伤诱导的新生内膜形成。VEGF 中和抗体的给药也减弱了线损伤诱导的新生内膜形成和巨噬细胞浸润。在原代培养的 AFs 中,外源性 VEGF 以时间和剂量依赖的方式增加 VEGF 的表达和分泌。AF 条件培养基促进内皮细胞血管生成、血管细胞黏附分子-1 的表达,而 VEGF 中和抗体和 VEGFR2 抑制剂 ZM323881 阻断了巨噬细胞黏附,也抑制了 VEGFR2/ERK1/2 通路的激活。

结论

这些结果表明,AF 衍生的 VEGF 在血管腔数量的增加中起重要作用,这涉及巨噬细胞募集和新生内膜形成。

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