Interferon-alpha 2 counteracts interleukin-1 alpha-stimulated expression of urokinase-type plasminogen activator in human foreskin microvascular endothelial cells in vitro.

Lymphokine and cytokine research Pub Date : 1994-04-01
J Wojta, H Zoellner, M Gallicchio, E L Filonzi, J A Hamilton, K McGrath
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Abstract

We investigated the effect of interferon-alpha 2 (IFN-alpha 2) on interleukin-1 alpha (IL-1 alpha)-induced up-regulation of urokinase type plasminogen activator (u-PA) expression in human foreskin microvascular endothelial cells (HFMEC) and human umbilical vein endothelial cells (HUVEC) in vitro. When IFN-alpha 2 and IL-1 alpha were added to the cells simultaneously, IFN-alpha 2 inhibited IL-1 alpha-induced up-regulation of u-PA antigen in a dose- and time-dependent fashion in HFMEC, whereas in HUVEC no effect of IFN-alpha 2 on IL-1 alpha-induced u-PA was seen. IL-1 alpha-induced up-regulation of PAI-1 antigen in HFMEC was not counteracted by IFN-alpha 2. When IFN-alpha 2 was added to HFMEC 1 or 2 h after IL-1 alpha a significant inhibition in u-PA synthesis was seen, whereas when IFN-alpha 2 was added to the cells 8 h after IL-1 alpha no effect on the induction of u-PA synthesis by IL-1 alpha was seen. IFN-alpha 2 also inhibited significantly the IL-1 alpha stimulated up-regulation of specific u-PA mRNA expression. In conclusion, our data show that IFN-alpha 2 can counteract the IL-1 alpha-induced up-regulation of u-PA in a similar way as IFN-gamma. This effect, which seems to be specific for microvascular endothelial cells, could contribute to the modulation of endothelial cell-mediated extravascular proteolysis in processes such as wound healing, neovascularisation, and endothelial cell migration.

干扰素- α 2抵消白细胞介素-1 α刺激的尿激酶型纤溶酶原激活物在体外人包皮微血管内皮细胞中的表达。
体外研究干扰素- α 2 (ifn - α 2)对白细胞介素-1 α (IL-1 α)诱导的人包皮微血管内皮细胞(HFMEC)和人脐静脉内皮细胞(HUVEC)尿激酶型纤溶酶原激活物(u-PA)表达上调的影响。当ifn - α 2和IL-1 α同时加入细胞时,ifn - α 2在HFMEC中以剂量和时间依赖性的方式抑制IL-1 α诱导的u-PA抗原上调,而在HUVEC中,ifn - α 2对IL-1 α诱导的u-PA没有影响。IL-1 α诱导的PAI-1抗原在HFMEC中的上调不被ifn - α 2抵消。当ifn - α 2添加到HFMEC 1或IL-1 α后2 h时,观察到对u-PA合成的显著抑制,而当IL-1 α后8 h时,观察到ifn - α 2对IL-1 α诱导u-PA合成的影响。ifn - α 2也显著抑制IL-1 α刺激的特异性u-PA mRNA表达上调。总之,我们的数据表明,ifn - α 2可以抵消IL-1 α诱导的u-PA上调,其方式与ifn - γ相似。这种效应似乎是微血管内皮细胞所特有的,可能有助于在伤口愈合、新生血管形成和内皮细胞迁移等过程中调节内皮细胞介导的血管外蛋白水解。
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