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Guanylate-Binding Protein-1 Expression Is Selectively Induced by Inflammatory Cytokines and Is an Activation Marker of Endothelial Cells during Inflammatory Diseases

机译:鸟嘌呤结合蛋白-1表达是由炎性细胞因子选择性诱导的,并且是炎性疾病期间内皮细胞的激活标记。

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摘要

During angiogenesis and inflammatory processes, endothelial cells acquire different activation phenotypes, whose identification may help in understanding the complex network of angiogenic and inflammatory interactions in vivo. To this goal we investigated the expression of the human guanylate-binding protein (GBP)-1 that is highly induced by inflammatory cytokines (ICs) and, therefore, may characterize IC-activated cells. Using a new rat monoclonal antibody raised against GBP-1, we show that GBP-1 is a cytoplasmic protein and that its expression in endothelial cells is selectively induced by interferon-γ, interleukin-1α, interleukin-1β, or tumor necrosis factor-α, but not by other cytokines, chemokines, or growth factors. Moreover, we found that GBP-1 expression is highly associated with vascular endothelial cells as confirmed by the simultaneous detection of GBP-1 and the endothelial cell-associated marker CD31 in a broad range of human tissues. Notably, GBP-1 expression was undetectable in the skin, but it was highly induced in vessels of skin diseases with a high-inflammatory component including psoriasis, adverse drug reactions, and Kaposi’s sarcoma. These results indicate that GBP-1 is a novel cellular activation marker that characterizes the IC-activated phenotype of endothelial cells.
机译:在血管生成和炎症过程中,内皮细胞获得不同的激活表型,其识别可能有助于理解体内复杂的血管生成和炎症相互作用网络。为此,我们研究了由炎性细胞因子(IC)高度诱导的人鸟苷酸结合蛋白(GBP)-1的表达,因此可表征IC激活的细胞。使用针对GBP-1的大鼠新单克隆抗体,我们显示GBP-1是一种细胞质蛋白,其在内皮细胞中的表达是由干扰素-γ,白介素-1α,白介素-1β或肿瘤坏死因子-选择性诱导的。 α,但不受其他细胞因子,趋化因子或生长因子的影响。此外,我们发现,GBP-1的表达与血管内皮细胞高度相关,这一点已通过在广泛的人体组织中同时检测到GBP-1和与内皮细胞相关的标记CD31来证实。值得注意的是,GBP-1在皮肤中无法检测到,但在具有高度炎症成分的皮肤疾病血管中被高度诱导,包括牛皮癣,药物不良反应和卡波济肉瘤。这些结果表明,GBP-1是一种新型的细胞激活标记物,可表征内皮细胞的IC激活表型。

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