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肿瘤坏死因子-α利用一种蛋白酪氨酸磷酸酶来抑制肝细胞生长因子受体的激活以及肝细胞生长因子诱导的内皮细胞增殖。

TNF-alpha employs a protein-tyrosine phosphatase to inhibit activation of hepatocyte growth factor receptor and hepatocyte growth factor-induced endothelial cell proliferation.

作者信息

Sugano Masahiro, Iwasaki Yoshiko, Abe Masako, Maeda Toyoki, Tsuchida Keiko, Makino Naoki

机构信息

Human Biology, Department of Health Science, Oita University of Nursing and Health Science, 2944 Megusuno, Oita, 870-1201, Japan.

出版信息

Mol Cell Biochem. 2009 Feb;322(1-2):113-7. doi: 10.1007/s11010-008-9946-7. Epub 2008 Nov 12.

Abstract

TNF-alpha impairs endothelial cell growth and angiogenesis. The anti-angiogenic effects of TNF-alpha have mainly been explained by its modulating vascular endothelial growth factor (VEGF)-specific angiogenic pathway. Hepatocyte growth factor (HGF) also promotes the growth of vascular endothelial cells and the development of new blood vessels through interaction with its specific receptor, c-met. However, it is little known whether TNF-alpha interacts with the HGF system or not. In this study, we examined the effect of TNF-alpha on HGF receptor function. In human umbilical venous endothelial cells (HUVEC), TNF-alpha acutely inhibited the phosphorylation and activation of c-met induced by HGF. The ability of TNF-alpha to inhibit HGF-induced c-met activity was impaired by sodium orthovanadate, suggesting that the inhibitory effect of TNF-alpha was mediated by a protein-tyrosine phosphatase. Treatment of HUVEC with TNF-alpha impairs the ability of HGF to activate MAPK and Akt, and this effect was blocked by SOV. HGF-induced c-met responses specifically associated with endothelial cell proliferation and mitogen-activated protein kinase activation were also inhibited by TNF-alpha, and these were reversed by sodium orthovanadate. HGF-induced SHP-1 (a cytoplasmic protein-tyrosine phosphatase) and pretreatment of HUVEC with TNF-alpha prior to HGF treatment resulted in substantial increase in the amount of SHP-1. These data suggest that TNF-alpha employs a protein-tyrosine phosphatase and may exert its anti-angiogenic function in part by modulating the HGF-specific angiogenic pathway in pathological settings.

摘要

肿瘤坏死因子-α(TNF-α)会损害内皮细胞生长和血管生成。TNF-α的抗血管生成作用主要通过其调节血管内皮生长因子(VEGF)特异性血管生成途径来解释。肝细胞生长因子(HGF)也通过与其特异性受体c-met相互作用促进血管内皮细胞生长和新血管形成。然而,TNF-α是否与HGF系统相互作用尚不清楚。在本研究中,我们检测了TNF-α对HGF受体功能的影响。在人脐静脉内皮细胞(HUVEC)中,TNF-α可急性抑制HGF诱导的c-met磷酸化和激活。原钒酸钠可削弱TNF-α抑制HGF诱导的c-met活性的能力,提示TNF-α的抑制作用是由蛋白酪氨酸磷酸酶介导的。用TNF-α处理HUVEC会损害HGF激活丝裂原活化蛋白激酶(MAPK)和蛋白激酶B(Akt)的能力,而这种作用可被原钒酸钠阻断。TNF-α还抑制了HGF诱导的与内皮细胞增殖和丝裂原活化蛋白激酶激活特异性相关的c-met反应,而原钒酸钠可使其逆转。HGF诱导的含Src同源2结构域的蛋白酪氨酸磷酸酶-1(SHP-1,一种细胞质蛋白酪氨酸磷酸酶)以及在HGF处理前先用TNF-α预处理HUVEC,会导致SHP-1的量大幅增加。这些数据表明,TNF-α利用蛋白酪氨酸磷酸酶,可能在病理情况下通过调节HGF特异性血管生成途径部分发挥其抗血管生成功能。

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