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Chinese medicine Tongxinluo increases tight junction protein levels by inducing KLF5 expression in microvascular endothelial cells

机译:中药通心络通过诱导微血管内皮细胞中KLF5的表达提高紧密连接蛋白水平

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摘要

Tongxinluo (TXL) is a compound prescription formulated according to the meridian theory of traditional Chinese medicine. It may play an important role in cardiovascular protection by improving endothelial cell function. The aim of present study was to investigate whether endothelial protection with TXL is related to its regulation of tight junction protein expression. Human cardiac microvascular endothelial cells (HCMECs) were cultured and treated with 10(-7)moll(-1) angiotensin II (Ang II) and the different doses of TXL; the expression of tight junction proteins occludin, claudin, VE-cadherin and beta-catenin was determined by Western blotting and real-time PCR. Gain-of-function and loss-of-function of Kruppel-like factor 5 (KLF5) were carried out in HCMEC transfected with either KLF5 adenovirus pAd-KLF5 or siRNA specific for KLF5. Angiotensinogen transgenic mice were treated with TXL by oral administration of TXL of 0.75gkg(-1)day(-1), and immunohistochemical staining was performed with antioccludin, anticlaudin, anti-VE-cadherin, antibeta-catenin and anti-KLF5 antibodies. Ang II treatment significantly reduced the expression of tight junction proteins occludin, claudin, VE-cadherin and beta-catenin in cultured HCMECs. TXL pretreatment could abrogate the down-regulation of these tight junction proteins induced by Ang II. Ang II treatment also decreased KLF5 expression at the mRNA and protein levels; TXL pretreatment markedly reversed the inhibitory effect of Ang II on KLF5 expression. Gain-of-function and loss-of-function of KLF5 showed that KLF5 mediated the expression of tight junction proteins in HCMECs. TXL-enhanced expression of the tight junction proteins was mediated by KLF5. In angiotensinogen transgenic mice, TXL also increased the tight junction protein levels by inducing KLF5 expression. Chinese medicine TXL increases tight junction protein levels by inducing KLF5 expression in microvascular endothelial cells. Copyright (c) 2015 John Wiley & Sons, Ltd.
机译:通络络(TXL)是根据中医经络理论制定的复方。它可能通过改善内皮细胞功能在心血管保护中起重要作用。本研究的目的是研究TXL的内皮保护作用是否与其紧密连接蛋白表达的调节有关。培养人心脏微血管内皮细胞(HCMEC),并用10(-7)moll(-1)血管紧张素II(Ang II)和不同剂量的TXL处理; Western blotting和实时PCR检测紧密连接蛋白occludin,claudin,VE-cadherin和β-catenin的表达。在用KLF5腺病毒pAd-KLF5或对KLF5特异的siRNA转染的HCMEC中进行Kruppel样因子5(KLF5)的功能获得和功能丧失。口服0.75gkg(-1)day(-1)的TXL,用TXL处理血管紧张素原转基因小鼠,并用抗闭合蛋白,抗月桂蛋白,抗VE-钙粘蛋白,抗β-连环蛋白和抗KLF5抗体进行免疫组织化学染色。 Ang II处理可显着降低培养的HCMEC中紧密连接蛋白occludin,claudin,VE-cadherin和β-catenin的表达。 TXL预处理可以消除Ang II诱导的这些紧密连接蛋白的下调。 Ang II处理还降低了mRNA和蛋白质水平的KLF5表达。 TXL预处理显着逆转了Ang II对KLF5表达的抑制作用。 KLF5的功能获得和功能丧失表明KLF5介导了HCMEC中紧密连接蛋白的表达。紧密连接蛋白的TXL增强表达是由KLF5介导的。在血管紧张素原转基因小鼠中,TXL还通过诱导KLF5表达而增加了紧密连接蛋白水平。中药TXL通过诱导微血管内皮细胞中KLF5表达来增加紧密连接蛋白水平。版权所有(c)2015 John Wiley&Sons,Ltd.

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