Suppr超能文献

流体剪切应力通过内皮细胞中的MEK5-BMK1抑制TNF介导的JNK激活。

Fluid shear stress inhibits TNF-mediated JNK activation via MEK5-BMK1 in endothelial cells.

作者信息

Li Lingli, Tatake Revati J, Natarajan Kanchana, Taba Yoji, Garin Gwen, Tai Caspar, Leung Ed, Surapisitchat James, Yoshizumi Masanori, Yan Chen, Abe Jun-Ichi, Berk Bradford C

机构信息

Aab Cardiovascular Research Institute and Department of Medicine, University of Rochester School of Medicine and Dentistry, Box 706, 601 Elmwood Avenue, Rochester, NY 14642, USA.

出版信息

Biochem Biophys Res Commun. 2008 May 23;370(1):159-63. doi: 10.1016/j.bbrc.2008.03.051. Epub 2008 Mar 19.

Abstract

Steady laminar blood flow protects vessels from atherosclerosis. We showed that flow decreased tumor necrosis factor-alpha (TNF)-mediated VCAM1 expression in endothelial cells (EC) by inhibiting JNK. Here, we determined the relative roles of MEK1, MEK5 and their downstream kinases ERK1/2 and BMK1 (ERK5) in flow-mediated inhibition of JNK activation. Steady laminar flow (shear stress=12dyn/cm(2)) increased BMK1 and ERK1/2 activity in EC. Pre-exposing EC for 10min to flow inhibited TNF activation of JNK by 58%. A key role for BMK1, but not ERK1/2 was shown. (1) Incubation of EC with PD184352, at concentrations that blocked ERK1/2, but not BMK1, had no effect on flow inhibition of TNF-mediated JNK activation. (2) BIX02188, a MEK5-selective inhibitor, completely reversed the inhibitory effects of flow. These findings indicate that flow inhibits TNF-mediated signaling events in EC by a mechanism dependent on activation of MEK5-BMK1, but not MEK1-ERK1/2. These results support a key role for the MEK5-BMK1 signaling pathway in the atheroprotective effects of blood flow.

摘要

稳定的层流血液流动可保护血管免受动脉粥样硬化影响。我们发现,血流通过抑制JNK来降低肿瘤坏死因子-α(TNF)介导的内皮细胞(EC)中VCAM1的表达。在此,我们确定了MEK1、MEK5及其下游激酶ERK1/2和BMK1(ERK5)在血流介导的JNK激活抑制中的相对作用。稳定的层流(剪切应力 = 12dyn/cm²)可增加内皮细胞中BMK1和ERK1/2的活性。将内皮细胞预先暴露于血流10分钟可使TNF对JNK的激活抑制58%。结果表明BMK1起关键作用,而ERK1/2并非如此。(1)用PD184352孵育内皮细胞,其浓度可阻断ERK1/2但不阻断BMK1,对血流抑制TNF介导的JNK激活没有影响。(2)MEK5选择性抑制剂BIX02188完全逆转了血流的抑制作用。这些发现表明,血流通过一种依赖于MEK5 - BMK1而非MEK1 - ERK1/2激活的机制来抑制内皮细胞中TNF介导的信号事件。这些结果支持了MEK5 - BMK1信号通路在血流的抗动脉粥样硬化保护作用中起关键作用。

相似文献

3
Endothelial atheroprotective and anti-inflammatory mechanisms.内皮细胞的抗动脉粥样硬化和抗炎机制。
Ann N Y Acad Sci. 2001 Dec;947:93-109; discussion 109-11. doi: 10.1111/j.1749-6632.2001.tb03932.x.
9
Identification of pharmacological inhibitors of the MEK5/ERK5 pathway.MEK5/ERK5信号通路药理学抑制剂的鉴定
Biochem Biophys Res Commun. 2008 Dec 5;377(1):120-5. doi: 10.1016/j.bbrc.2008.09.087. Epub 2008 Oct 1.

引用本文的文献

1
Endothelial mechanobiology in atherosclerosis.动脉粥样硬化中的血管内皮力学。
Cardiovasc Res. 2023 Jul 6;119(8):1656-1675. doi: 10.1093/cvr/cvad076.
2
MEKK3-TGFβ crosstalk regulates inward arterial remodeling.MEKK3-TGFβ 串扰调节内向性动脉重构。
Proc Natl Acad Sci U S A. 2021 Dec 21;118(51). doi: 10.1073/pnas.2112625118.
7
Flow signaling and atherosclerosis.血流信号与动脉粥样硬化
Cell Mol Life Sci. 2017 May;74(10):1835-1858. doi: 10.1007/s00018-016-2442-4. Epub 2016 Dec 30.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验