Ding Mei, Yuan Ying-Jin
Department of Biotechnology, School of Chemistry and Chemical Engineering, Tianjin University of Technology, China.
J Pharm Pharmacol. 2007 Jul;59(7):1027-33. doi: 10.1211/jpp.59.7.0016.
Exposure of endothelial cells to tumour necrosis factor-alpha (TNF-alpha) results in increased endothelial permeability, accompanied by a loss of cell-cell adherence junctions. The importance of tyrosine phosphatase and kinase activity in oxidant-mediated loss of cell junction structures has been demonstrated. The purpose of this study was to determine whether tyrosine phosphorylation contributes to TNF-alpha-mediated disorganization of endothelial cell junctions and how an extract of Salvia miltiorrhiza (ESM) and its active ingredients, Danshensu (DSS) and salvianolic acid B (Sal B), exert their protective effect in maintaining cell integrity. Immunoblotting results indicated that TNF-alpha exposure resulted in tyrosine phosphorylation of junctional proteins such as vascular endothelial cadherin and beta-catenin, which was attenuated by ESM and its active ingredients DSS and Sal B. In addition, immunoprecipitation showed ESM and its active ingredients prevented beta-catenin disassociation from the cytoskeleton in TNF-alpha-treated human umbilical vein endothelial cells. The results suggest that TNF-alpha produced biological effects at least partly by junctional protein phosphotyrosine modifications by increasing the total cellular phosphorylation level. It could be concluded that ESM and its active ingredients were effective at eliminating the factors leading to the rise in cellular phosphorylation, thus helping to maintain the integrity of endothelial junction structure.
内皮细胞暴露于肿瘤坏死因子-α(TNF-α)会导致内皮通透性增加,并伴有细胞间黏附连接的丧失。酪氨酸磷酸酶和激酶活性在氧化剂介导的细胞连接结构丧失中的重要性已得到证实。本研究的目的是确定酪氨酸磷酸化是否促成TNF-α介导的内皮细胞连接紊乱,以及丹参提取物(ESM)及其活性成分丹酚酸(DSS)和丹酚酸B(Sal B)如何在维持细胞完整性方面发挥保护作用。免疫印迹结果表明,TNF-α暴露导致连接蛋白如血管内皮钙黏蛋白和β-连环蛋白的酪氨酸磷酸化,而ESM及其活性成分DSS和Sal B可使其减弱。此外,免疫沉淀显示ESM及其活性成分可防止β-连环蛋白在TNF-α处理的人脐静脉内皮细胞中与细胞骨架解离。结果表明,TNF-α至少部分通过增加细胞总磷酸化水平,对连接蛋白磷酸酪氨酸进行修饰而产生生物学效应。可以得出结论,ESM及其活性成分可有效消除导致细胞磷酸化增加的因素,从而有助于维持内皮连接结构的完整性。