González-Miguel Javier, Morchón Rodrigo, Mellado Isabel, Carretón Elena, Montoya-Alonso José Alberto, Simón Fernando
Laboratory of Parasitology, University of Salamanca, Avda. Campo Charro s/n, 37007, Salamanca, Spain.
Mol Biochem Parasitol. 2012 Feb;181(2):134-40. doi: 10.1016/j.molbiopara.2011.10.010. Epub 2011 Oct 25.
Dirofilaria immitis is the causative agent of canine and feline heartworm disease. The parasite can survive for long periods of time (7 years or more) in the circulatory system of immunocompetent reservoirs, producing usually a chronic inflammatory vascular disease. In addition, the simultaneous death of groups of adult worms can trigger an acute disease characterized by the exacerbation of inflammatory reactions and the emergence of serious thromboembolic events. In the context of the D. immitis/host relationships, the aim of this study was to investigate the interaction between the excretory/secretory antigens from D. immitis adult worms (DiES) and the fibrinolytic system of the host. Using an enzyme-linked immunosorbent assay we showed that DiES extract is able to bind plasminogen and generate plasmin, although this fact requires the presence of the tissue plasminogen activator (t-PA). Moreover, we established that DiES extract enhances t-PA expression in cultured vascular endothelial cells. Additionally, 10 plasminogen-binding proteins from DiES extract were identified by mass spectrometry (HSP60, actin-1/3, actin, actin 4, transglutaminase, GAPDH, Ov87, LOAG_14743, galectin and P22U). The data suggest that DiES antigens interact with the environment of the parasite regulating the activation of the fibrinolytic system of the host with involvement of the vascular endothelium in the process.
犬恶丝虫是犬猫心丝虫病的病原体。该寄生虫可在免疫功能正常的宿主体内循环系统中长期存活(7年或更长时间),通常引发慢性炎症性血管疾病。此外,成虫群体的同时死亡可引发一种急性疾病,其特征为炎症反应加剧和严重血栓栓塞事件的出现。在犬恶丝虫与宿主的关系背景下,本研究旨在探讨犬恶丝虫成虫排泄/分泌抗原(DiES)与宿主纤维蛋白溶解系统之间的相互作用。我们使用酶联免疫吸附测定法表明,DiES提取物能够结合纤溶酶原并生成纤溶酶,不过这一过程需要组织纤溶酶原激活物(t-PA)的存在。此外,我们证实DiES提取物可增强培养的血管内皮细胞中t-PA的表达。另外,通过质谱法鉴定出DiES提取物中的10种纤溶酶原结合蛋白(热休克蛋白60、肌动蛋白-1/3、肌动蛋白、肌动蛋白4、转谷氨酰胺酶、甘油醛-3-磷酸脱氢酶、Ov87、LOAG_14743、半乳糖凝集素和P22U)。数据表明,DiES抗原与寄生虫所处环境相互作用,在血管内皮细胞参与的过程中调节宿主纤维蛋白溶解系统的激活。