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首页> 外文期刊>Journal of periodontal research >Prevotella intermedia lipopolysaccharide stimulates release of nitric oxide by inducing expression of inducible nitric oxide synthase.
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Prevotella intermedia lipopolysaccharide stimulates release of nitric oxide by inducing expression of inducible nitric oxide synthase.

机译:中间小球藻脂多糖通过诱导诱导型一氧化氮合酶的表达来刺激一氧化氮的释放。

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Kim S-J, Ha M-S, Choi E-Y, Choi J-I, Choi I-S. Prevotella intermedia lipopolysaccharide stimulates release of nitric oxide by inducing expression of inducible nitric oxide synthase. J Periodont Res 2004; doi: 10.1111/j.1600-0765.2004.00757.x (c) Blackwell Munksgaard 2004Objectives: 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. Material and methods: 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. Results: 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. Conclusions: 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.
机译:Kim S-J,Ha M-S,Choi E-Y,Choi J-I,Choi I-S。中间小球藻脂多糖通过诱导诱导型一氧化氮合酶的表达来刺激一氧化氮的释放。 J牙周病杂志2004; doi:10.1111 / j.1600-0765.2004.00757.x(c)Blackwell Munksgaard 2004年目标:本研究的目的是研究来自炎性牙周病主要病因中间媒介普氏杆菌的脂多糖对一氧化氮产生的影响。 (NO)和诱导型一氧化氮合酶(iNOS)在小鼠巨噬细胞RAW264.7中的表达。我们还试图阐明参与中间脂球菌脂多糖诱导的NO产生的信号传导机制。材料和方法:通过标准的热酚水法,从中间疟原虫ATCC 25611制备脂多糖。通过测量培养物上清液中亚硝酸盐的积累来测定NO的产生。进行了iNOS的蛋白质印迹分析和逆转录-聚合酶链反应(RT-PCR)产物的分析。结果:我们发现中间疟原虫脂多糖可以诱导iNOS表达并刺激NO的释放,而没有其他刺激,并且证明了转录因子核因子-κB(NF-κB)和微管聚合在NO产生中的重要作用。 NO的产生需要1-精氨酸,但不需要激活蛋白激酶C或蛋白酪氨酸激酶。结论:本研究清楚地显示,在没有其他刺激的情况下,中间脂多糖完全诱导RAW264.7细胞中iNOS的表达和NO的产生。中间疟原虫脂多糖促进NO产生的能力在炎性牙周病的发病机理中可能是重要的。

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