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MKP-7,JNK 的负调控因子,通过 IRF-1 调节 VCAM-1 的表达。

MKP-7, a negative regulator of JNK, regulates VCAM-1 expression through IRF-1.

机构信息

Department of Pharmacology, School of Medicine, Institute of Health Sciences, Gyeongsang National University, Jinju, Republic of Korea.

出版信息

Cell Signal. 2012 Apr;24(4):866-72. doi: 10.1016/j.cellsig.2011.12.002. Epub 2011 Dec 13.

Abstract

Cell adhesion molecules (CAMs) are involved in a variety of pathologies including cancer, inflammation, pathogenic infections and autoimmune disease. In particular, VCAM-1, rather than ICAM-1, plays a major role in the initiation of atherosclerosis and tumor progression. Therefore, we attempted to elucidate differential mechanisms that regulate VCAM-1 and ICAM-1 expressions. Down-regulation of JNK by a specific inhibitor (SP600125) or dominant negative (DN) JNK1 plasmid enhanced TNF-α-induced VCAM-1 but not ICAM-1 expression. Moreover, transfection with a JNK1-overexpressing vector resulted in the inhibition of VCAM-1 expression stimulated by TNF-α in HUVECs, suggesting that JNK negatively regulates TNF-α-induced VCAM-1 expression in endothelial cells (ECs). Next, we investigated whether JNK signaling affects IRF-1 and/or GATA6, which are transcription factors that mediate TNF-α induction of VCAM-1 but not ICAM-1. The DN-JNK1 plasmid-transfected cells enhanced TNF-α up-regulation of IRF-1 whereas JNK1-overexpressing cells displayed down-regulation; however, neither DN-JNK1 transfection nor JNK1 overexpression affected GATA6 protein levels in the nuclear fraction. Chromatin immunoprecipitation (ChIP) assay confirmed that the inhibition of JNK by DN-JNK1 transfection increases the binding of IRF-1 to the VCAM-1 promoter whereas the overexpression of JNK1 inhibits IRF-1 binding to the VCAM-1 promoter. However, neither DN-JNK1 nor JNK1 overexpression altered GATA6 affinity for the VCAM-1 promoter region. We also examined whether MKP-7 affects ICAM-1 or VCAM-1 by regulating JNK. TNF-α-induced phosphor-JNK levels increased after 5min, peaked at 10 min, and decreased after 30 min. Interestingly, MKP-7 protein levels increased after 30 min, when phosphor-JNK induction by TNF-α was decreased. In addition, silencing MKP-7 with specific siRNA resulted in an increase in phosphor-JNK and inhibited the expression of VCAM-1 but not ICAM-1. Moreover, silencing MKP-7 caused the down-regulation of IRF-1 protein levels and binding to the VCAM-1 promoter. Thus, we suggest that MKP-7, a negative regulator of JNK, regulates VCAM-1 expression in activated endothelial cells through IRF-1 but not GATA6.

摘要

细胞黏附分子(CAMs)参与多种病理学过程,包括癌症、炎症、致病性感染和自身免疫性疾病。特别是 VCAM-1,而不是 ICAM-1,在动脉粥样硬化和肿瘤进展的启动中起主要作用。因此,我们试图阐明调节 VCAM-1 和 ICAM-1 表达的差异机制。用特异性抑制剂(SP600125)或显性负(DN)JNK1 质粒下调 JNK 可增强 TNF-α诱导的 VCAM-1 表达,但不增强 ICAM-1 表达。此外,转染 JNK1 过表达载体可抑制 TNF-α刺激的 HUVECs 中 VCAM-1 的表达,表明 JNK 负调节内皮细胞(ECs)中 TNF-α诱导的 VCAM-1 表达。接下来,我们研究了 JNK 信号是否影响 IRF-1 和/或 GATA6,IRF-1 和 GATA6 是介导 TNF-α诱导 VCAM-1 表达但不介导 ICAM-1 表达的转录因子。转染 DN-JNK1 质粒的细胞增强了 TNF-α对 IRF-1 的上调,而 JNK1 过表达细胞显示下调;然而,DN-JNK1 转染或 JNK1 过表达均不影响核部分 GATA6 蛋白水平。染色质免疫沉淀(ChIP)实验证实,DN-JNK1 转染抑制 JNK 可增加 IRF-1 与 VCAM-1 启动子的结合,而 JNK1 过表达抑制 IRF-1 与 VCAM-1 启动子的结合。然而,DN-JNK1 或 JNK1 过表达均不改变 GATA6 对 VCAM-1 启动子区域的亲和力。我们还研究了 MKP-7 是否通过调节 JNK 来影响 ICAM-1 或 VCAM-1。TNF-α 诱导的 phosphor-JNK 水平在 5 分钟后增加,在 10 分钟时达到峰值,在 30 分钟后减少。有趣的是,当 TNF-α 诱导的 phosphor-JNK 减少时,MKP-7 蛋白水平在 30 分钟后增加。此外,用特异性 siRNA 沉默 MKP-7 会增加 phosphor-JNK 并抑制 VCAM-1 的表达,但不抑制 ICAM-1 的表达。此外,沉默 MKP-7 导致 IRF-1 蛋白水平下调并抑制结合到 VCAM-1 启动子。因此,我们认为,作为 JNK 的负调节剂,MKP-7 通过 IRF-1 而不是 GATA6 调节活化的内皮细胞中 VCAM-1 的表达。

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