首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Protease-activated receptor-2 activation: a major role in the pathogenesis of porphyromonas gingivalis infection.
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Protease-activated receptor-2 activation: a major role in the pathogenesis of porphyromonas gingivalis infection.

机译:蛋白酶激活的受体2激活:牙龈卟啉单胞菌感染的发病机理中的主要作用。

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摘要

We have investigated the specific contribution of protease-activated receptor-2 (PAR(2)) to host defense during Porphyromonas gingivalis infection. Culture supernatants from P. gingivalis strains 33277 and W50 provoked Ca(2+) mobilization in cells transfected with PAR(2) (PAR(2)-KNRK) and desensitized the subsequent responses to PAR(2)-selective agonist. In addition, culture supernatants of P. gingivalis E8 (RgpA/RgpB double knockout) did not cause calcium response in PAR(2)-KNRK cells, evidencing the involvement of the arginine-specific cysteine proteases RgpA and RgpB in PAR(2) activation by P. gingivalis. Injection of P. gingivalis into mouse subcutaneous chambers provoked an increased proteolytic activity, which was inhibited by serine protease inhibitors. Fluids collected from chambers of P. gingivalis-injected mice were able to activate PAR(2) and this activation was inhibited by serine protease inhibitors. P. gingivalis inoculation into subcutaneous chambers of wild-type mice induced an inflammatory response that was inhibited by a serine protease inhibitor and was significantly reduced in PAR(2)-deficient mice. Finally, mice orally challenged with P. gingivalis developed alveolar bone loss, which was significantly reduced in PAR(2)-deficient mice at 42 and 60 days after P. gingivalis infection. We conclude that PAR(2) is activated on P. gingivalis infection, in which it plays an important role in the host inflammatory response.
机译:我们已经研究了牙龈卟啉单胞菌感染过程中蛋白酶激活受体2(PAR(2))对宿主防御的具体贡献。从牙龈卟啉单胞菌菌株33277和W50的培养上清液在用PAR(2)(PAR(2)-KNRK)转染的细胞中引起Ca(2+)动员,并使对PAR(2)选择性激动剂的后续反应不敏感。此外,牙龈卟啉单胞菌E8(RgpA / RgpB双敲除)的培养上清液不会在PAR(2)-KNRK细胞中引起钙反应,证明精氨酸特异性半胱氨酸蛋白酶RgpA和RgpB参与了PAR(2)激活。由P. gingivalis。将牙龈卟啉单胞菌注射到小鼠皮下腔室中引起蛋白水解活性的提高,其被丝氨酸蛋白酶抑制剂抑制。从注射牙龈卟啉单胞菌的小鼠的小室收集的液体能够激活PAR(2),并且这种激活被丝氨酸蛋白酶抑制剂抑制。牙龈卟啉单胞菌接种到野生型小鼠的皮下室诱导炎症反应,被丝氨酸蛋白酶抑制剂抑制,并在PAR(2)缺陷小鼠中显着减少。最后,口服牙龈卟啉单胞菌攻击的小鼠发展了牙槽骨丢失,在牙龈卟啉单胞菌感染后第42天和60天,PAR(2)缺陷型小鼠的牙槽骨损失明显减少。我们得出的结论是,PAR(2)在牙龈卟啉单胞菌感染上被激活,其中它在宿主炎症反应中起重要作用。

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