Kim Sung-Jo, Ha Mi-Suk, Choi Eun-Young, Choi Jeom-Il, Choi In-Soon
Department of Periodontology, College of Dentistry, Pusan National University, Busan, South Korea.
J Periodontal Res. 2004 Dec;39(6):424-31. doi: 10.1111/j.1600-0765.2004.00757.x.
The purpose of this study was to examine the effects of lipopolysaccharide from Prevotella intermedia, a major cause of inflammatory periodontal disease, on the production of nitric oxide (NO) and expression of inducible nitric oxide synthase (iNOS) in the murine macrophage cell line RAW264.7. We also attempted to throw light on the signaling mechanisms involved in P. intermedia lipopolysaccharide-induced NO production.
Lipopolysaccharide from P. intermedia ATCC 25611 was prepared by the standard hot phenol-water method. NO production was assayed by measuring the accumulation of nitrite in culture supernatants. Western blot analysis of iNOS and analysis of reverse transcription-polymerase chain reaction (RT-PCR) products were carried out.
We found that P. intermedia lipopolysaccharide can induce iNOS expression and stimulate the release of NO without additional stimuli and demonstrated an important role of the transcription factor nuclear factor-kappaB (NF-kappaB) and microtubule polymerization in NO production. The production of NO required l-arginine but not activation of protein kinase C or protein tyrosine kinase.
The present study clearly shows that P. intermedia lipopolysaccharide fully induced iNOS expression and NO production in RAW264.7 cells in the absence of other stimuli. The ability of P. intermedia lipopolysaccharide to promote the production of NO may be important in the pathogenesis of inflammatory periodontal disease.
本研究旨在探讨牙龈卟啉单胞菌(一种炎症性牙周病的主要病因)的脂多糖对小鼠巨噬细胞系RAW264.7中一氧化氮(NO)生成及诱导型一氧化氮合酶(iNOS)表达的影响。我们还试图阐明牙龈卟啉单胞菌脂多糖诱导NO生成所涉及的信号传导机制。
采用标准热酚 - 水法制备牙龈卟啉单胞菌ATCC 25611的脂多糖。通过测量培养上清液中亚硝酸盐的积累来检测NO的生成。进行了iNOS的蛋白质印迹分析以及逆转录 - 聚合酶链反应(RT - PCR)产物分析。
我们发现牙龈卟啉单胞菌脂多糖无需额外刺激即可诱导iNOS表达并刺激NO释放,并证明转录因子核因子 - κB(NF - κB)和微管聚合在NO生成中起重要作用。NO的生成需要L - 精氨酸,但不需要蛋白激酶C或蛋白酪氨酸激酶的激活。
本研究清楚地表明,牙龈卟啉单胞菌脂多糖在无其他刺激的情况下能在RAW264.7细胞中充分诱导iNOS表达和NO生成。牙龈卟啉单胞菌脂多糖促进NO生成的能力在炎症性牙周病的发病机制中可能很重要。