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骨桥蛋白和整合素β3启动子低甲基化与大隐静脉曲张中血管平滑肌细胞表型转换的关系。

Association between the hypomethylation of osteopontin and integrin β3 promoters and vascular smooth muscle cell phenotype switching in great saphenous varicose veins.

作者信息

Jiang Han, Lun Yu, Wu Xiaoyu, Xia Qian, Zhang Xiaoyu, Xin Shijie, Zhang Jian

机构信息

Department of Vascular and Thyroid Surgery, the First Affiliated Hospital of China Medical University, Shenyang 110001, China.

出版信息

Int J Mol Sci. 2014 Oct 17;15(10):18747-61. doi: 10.3390/ijms151018747.

Abstract

Lower extremity varicose veins are a common condition in vascular surgery and proliferation of vascular smooth muscle cells (VSMCs) in the intima is a significant pathological feature of varicosity. However, the pathogenesis of varicose veins is not fully understood. Osteopontin (OPN) could promote the migration and adhesion of VSMCs through the cell surface receptor integrin β3 and the cooperation of OPN and integrin β3 is involved in many vascular diseases. However, the role of OPN and integrin β3 in varicosity remains unclear. In the current study, we found that the methylation levels in the promoter regions of OPN and integrin β3 genes in the VSMCs of varicose veins are reduced and the protein expression of OPN and integrin β3 are increased, compared with normal veins. Furthermore, it was observed that VSMCs in the neointima of varicose veins were transformed into the synthetic phenotype. Collectively, hypomethylation of the promoter regions for OPN and integrin β3 genes may increase the expression of these genes in varicosity, which is closely related to VSMC phenotype switching. Hypomethylation of the promoter regions for OPN and integrin β3 genes may be a key factor in the pathogenesis of varicosity.

摘要

下肢静脉曲张是血管外科的常见病症,内膜中血管平滑肌细胞(VSMC)的增殖是静脉曲张的一个重要病理特征。然而,静脉曲张的发病机制尚未完全明确。骨桥蛋白(OPN)可通过细胞表面受体整合素β3促进VSMC的迁移和黏附,OPN与整合素β3的协同作用参与了许多血管疾病。然而,OPN和整合素β3在静脉曲张中的作用仍不清楚。在本研究中,我们发现与正常静脉相比,静脉曲张VSMC中OPN和整合素β3基因启动子区域的甲基化水平降低,OPN和整合素β3的蛋白表达增加。此外,观察到静脉曲张新生内膜中的VSMC转变为合成表型。总体而言,OPN和整合素β3基因启动子区域的低甲基化可能会增加这些基因在静脉曲张中的表达,这与VSMC表型转换密切相关。OPN和整合素β3基因启动子区域的低甲基化可能是静脉曲张发病机制中的一个关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6dc/4227244/8ef4bb633d79/ijms-15-18747-g001.jpg

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