首页> 外文期刊>Veterinary Parasitology >Adult Dirofilaria immitis excretory/secretory antigens upregulate the production of prostaglandin E2 and downregulate monocyte transmigration in an 'in vitro' model of vascular endothelial cell cultures
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Adult Dirofilaria immitis excretory/secretory antigens upregulate the production of prostaglandin E2 and downregulate monocyte transmigration in an 'in vitro' model of vascular endothelial cell cultures

机译:在血管内皮细胞培养的“体外”模型中,成年丝状体丝状体炎性分泌/分泌抗原上调前列腺素E2的产生并下调单核细胞的迁移。

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Canine and feline cardiopulmonary dirofilariosis caused by Dirofilaria immitis is a chronic and potentially fatal disease. Adult worms live in the pulmonary arteries of infected immunocompetent hosts for years. The aim of the present study is the identification of the influence of the metabolic products (excretory/secretory antigens, DiE/S) of D. immitis on the vascular endothelial cells, because the vascular endothelium interplays in a direct manner with the parasite and their products. For this purpose, HAAE-1 vascular endothelial cells were treated with DiE/S, using non-treated cultures as negative controls. Significant increases in the COX-2, 5-LO expression and PGE(2) level were detected in the treated cells compared with the control cells. Moreover, DiE/S decreases monocyte transmigrations across vascular endothelial cell monolayers. Treatment with DiE/S does not have a cytotoxic effect and do not alter apoptosis, necrosis or cell cycle of vascular endothelial cells. These results suggest that the DiE/S stimulates the production of mediators and mechanisms that favor the survival of the parasite, in vascular endothelial cells, contributing to restrict vascular and lung damages in the infected host, without altering the basic physiologic processes of endothelial cells. (C) 2010 Elsevier B.V. All rights reserved.
机译:由Dirofilaria免疫炎引起的犬和猫心肺丝虫病是一种慢性且可能致命的疾病。成年蠕虫在感染了免疫能力的宿主的肺动脉中生活了多年。本研究的目的是鉴定D. Immitis的代谢产物(排泄/分泌抗原,DiE / S)对血管内皮细胞的影响,因为血管内皮与寄生虫及其寄生虫直接相互作用。产品。为此,使用未经处理的培养物作为阴性对照,用DiE / S处理HAAE-1血管内皮细胞。与对照细胞相比,在处理过的细胞中检测到COX-2、5-LO表达和PGE(2)水平显着增加。此外,DiE / S减少了单核细胞跨血管内皮细胞单层的迁移。用DiE / S进行治疗不会产生细胞毒性作用,也不会改变血管内皮细胞的凋亡,坏死或细胞周期。这些结果表明,DiE / S刺激了血管内皮细胞中介导物的产生和有利于寄生虫存活的机制,有助于限制受感染宿主的血管和肺部损伤,而没有改变内皮细胞的基本生理过程。 (C)2010 Elsevier B.V.保留所有权利。

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