首页> 美国卫生研究院文献>Infection and Immunity >Effect of free and vesicle-bound cysteine proteinases of Porphyromonas gingivalis on plasma clot formation: implications for bleeding tendency at periodontitis sites.
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Effect of free and vesicle-bound cysteine proteinases of Porphyromonas gingivalis on plasma clot formation: implications for bleeding tendency at periodontitis sites.

机译:牙龈卟啉单胞菌的游离和囊泡结合的半胱氨酸蛋白酶对血浆凝块形成的影响:对牙周炎部位出血趋势的影响。

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摘要

Infection by Porphyromonas gingivalis is strongly associated with adult periodontitis, with proteinases from this bacterium now considered to be important virulence factors. In order to investigate possible pathological functions of these enzymes, we examined the effect of both free and vesicle-bound forms of the two major cysteine proteinases (gingipains) of P. gingivalis on plasma clot formation by using thrombin time (TT) measurements. Both Lys-gingipain (gingipain-K) and Arg-gingipain (gingipain-R) prolonged plasma TT in a dose- and time-dependent manner, and this was also found with vesicles which are the biological carriers of P. gingivalis proteinases. The increase in plasma TT by vesicles could be completely reversed by treatment with nonspecific cysteine proteinase inhibitors but only partially by compounds selective for either gingipain-K or gingipain-R. Preincubation of vesicles with a gingipain-K-specific inhibitor (z-FK-ck) reduced plasma TT more than a gingipain-R-specific inhibitor (leupeptin), suggesting that under physiological conditions gingipain-K was more effective in fibrinogen destruction. Each purified enzyme also markedly increased fibrinogen TT, gingipain-R being fourfold more potent than gingipain-K. However, in plasma, gingipain-R was ineffective because of the inhibitory effect of albumin. These results imply that cysteine proteinases, especially gingipain-K, abrogate the clotting potential of fibrinogen and, therefore, may contribute to the bleeding tendency and to persistent inflammation in periodontitis sites infected with P. gingivalis.
机译:牙龈卟啉单胞菌的感染与成人牙周炎密切相关,这种细菌的蛋白酶现在被认为是重要的毒力因子。为了研究这些酶的可能病理功能,我们通过凝血酶时间(TT)测量检查了牙龈卟啉单胞菌的两种主要半胱氨酸蛋白酶(姜黄素)的游离形式和囊泡结合形式对血浆凝块形成的影响。 Lys-gingipain(gingipain-K)和Arg-gingipain(gingipain-R)都以剂量和时间依赖性方式延长血浆TT,这也被作为牙龈卟啉单胞菌蛋白酶生物载体的囊泡发现。通过使用非特异性半胱氨酸蛋白酶抑制剂治疗可以完全逆转囊泡血浆TT的增加,但只能通过对gingipain-K或gingipain-R选择性的化合物来部分逆转。与gingipain-K特异性抑制剂(z-FK-ck)预孵育的囊泡比gingipain-R特异性抑制剂(leupeptin)降低的血浆TT值更多,这表明在生理条件下gingipain-K在破坏纤维蛋白原方面更有效。每种纯化的酶也显着增加血纤蛋白原TT,而gingipain-R的效力是gingipain-K的四倍。但是,在血浆中,由于白蛋白的抑制作用,gingipain-R无效。这些结果暗示半胱氨酸蛋白酶,特别是gingipain-K,消除了纤维蛋白原的凝结潜能,因此,可能有助于在感染牙龈卟啉单胞菌的牙周炎部位的出血趋势和持续的炎症。

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