Choi E-Y, Hwang Y-M, Lee J-Y, Choi J-I, Choi I-S, Jin J-Y, Ko J S, Kim S-J
Department of Life Science, College of Natural Science, Silla University, Busan, Korea.
J Periodontal Res. 2007 Aug;42(4):350-60. doi: 10.1111/j.1600-0765.2006.00956.x.
The purpose of this study was to examine the effects of lipid A-associated proteins from Porphyromonas gingivalis, a major cause of inflammatory periodontal disease, on the production of nitric oxide and expression of inducible nitric oxide synthase in the murine macrophage cell line, RAW264.7. We also attempted to throw light on the signaling mechanisms involved in P. gingivalis lipid A-associated protein-induced nitric oxide production.
The lipid A-associated proteins from P. gingivalis 381 were prepared by standard hot phenol-water extraction of endotoxin isolated by the butanol method. Nitric oxide production was assayed by measuring the accumulation of nitrite in culture supernatants. Western blot analysis of inducible nitric oxide synthase and analysis of reverse transcription-polymerase chain reaction products were carried out.
We found that P. gingivalis lipid A-associated proteins can induce inducible nitric oxide synthase expression and stimulate the release of nitric oxide without additional stimuli, and we demonstrated that multiple signaling pathways, such as nuclear factor-kappaB, microtubule polymerization, protein tyrosine kinase, protein kinase C, and mitogen-activated protein kinase cascades, are involved in P. gingivalis lipid A-associated protein-stimulated nitric oxide production. The production of nitric oxide required l-arginine.
The present study clearly shows that P. gingivalis lipid A-associated proteins fully induced inducible nitric oxide synthase expression and nitric oxide production in RAW264.7 cells in the absence of other stimuli. The ability of P. gingivalis lipid A-associated proteins to promote the production of nitric oxide may be important in the pathogenesis of inflammatory periodontal disease.
本研究旨在检测牙龈卟啉单胞菌(炎症性牙周病的主要病因)的脂多糖相关蛋白对小鼠巨噬细胞系RAW264.7中一氧化氮产生及诱导型一氧化氮合酶表达的影响。我们还试图阐明牙龈卟啉单胞菌脂多糖相关蛋白诱导一氧化氮产生所涉及的信号传导机制。
采用标准热酚 - 水法从经丁醇法分离的内毒素中制备牙龈卟啉单胞菌381的脂多糖相关蛋白。通过测量培养上清液中亚硝酸盐的积累来检测一氧化氮的产生。进行诱导型一氧化氮合酶的蛋白质印迹分析及逆转录 - 聚合酶链反应产物分析。
我们发现牙龈卟啉单胞菌脂多糖相关蛋白无需额外刺激即可诱导诱导型一氧化氮合酶表达并刺激一氧化氮释放,并且我们证明多种信号通路,如核因子 - κB、微管聚合、蛋白酪氨酸激酶、蛋白激酶C和丝裂原活化蛋白激酶级联反应,均参与牙龈卟啉单胞菌脂多糖相关蛋白刺激的一氧化氮产生。一氧化氮的产生需要L - 精氨酸。
本研究清楚地表明,牙龈卟啉单胞菌脂多糖相关蛋白在无其他刺激的情况下可在RAW264.7细胞中充分诱导诱导型一氧化氮合酶表达及一氧化氮产生。牙龈卟啉单胞菌脂多糖相关蛋白促进一氧化氮产生的能力在炎症性牙周病的发病机制中可能很重要。