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中间普氏菌脂多糖通过丝裂原活化蛋白激酶信号通路刺激单核细胞衍生巨噬细胞释放肿瘤坏死因子-α。

Prevotella intermedia lipopolysaccharide stimulates release of tumor necrosis factor-alpha through mitogen-activated protein kinase signaling pathways in monocyte-derived macrophages.

作者信息

Kim Sung-Jo, Choi Eun-Young, Kim Eun Gyung, Shin Su-Hwa, Lee Ju-Youn, Choi Jeom-Il, Choi In-Soon

机构信息

Department of Periodontology, College of Dentistry, Pusan National University, Busan, Korea.

出版信息

FEMS Immunol Med Microbiol. 2007 Nov;51(2):407-13. doi: 10.1111/j.1574-695X.2007.00318.x. Epub 2007 Aug 29.

DOI:10.1111/j.1574-695X.2007.00318.x
PMID:17727652
Abstract

The purpose of this study was to investigate the effects of lipopolysaccharide from Prevotella intermedia, a major cause of inflammatory periodontal disease, on the production of tumor necrosis factor (TNF)-alpha and the expression of TNF-alpha mRNA in differentiated THP-1 cells, a human monocytic cell line. The potential involvement of the three main mitogen-activated protein kinase (MAPK) signaling pathways in the induction of TNF-alpha production was also investigated. Lipopolysaccharide from P. intermedia ATCC 25611 was prepared by the standard hot phenol-water method. THP-1 cells were incubated in the medium supplemented with phorbol myristate acetate to induce differentiation into macrophage-like cells. It was found that P. intermedia lipopolysaccharide can induce TNF-alpha mRNA expression and stimulate the release of TNF-alpha in differentiated THP-1 cells without additional stimuli. Treatment of the cells with P. intermedia lipopolysaccharide resulted in a simultaneous activation of three MAPKs [extracellular signal-related kinase 1/2 (ERK1/2), c-Jun N-terminal kinase 1/2 (JNK1/2) and p38]. Pretreatment of the cells with MAPK inhibitors effectively suppressed P. intermedia lipopolysaccharide-induced TNF-alpha production without affecting the expression of TNF-alpha mRNA. These data thus provided good evidence that the MAPK signaling pathways are required for the regulation of P. intermedia lipopolysaccharide-induced TNF-alpha synthesis at the level of translation more than at the transcriptional level.

摘要

本研究的目的是探讨中间普氏菌(炎症性牙周病的主要病因)的脂多糖对人单核细胞系分化的THP-1细胞中肿瘤坏死因子(TNF)-α产生及TNF-α mRNA表达的影响。还研究了三种主要的丝裂原活化蛋白激酶(MAPK)信号通路在诱导TNF-α产生中的潜在作用。通过标准热酚-水法制备中间普氏菌ATCC 25611的脂多糖。将THP-1细胞在补充有佛波酯肉豆蔻酸酯乙酸盐的培养基中孵育以诱导分化为巨噬细胞样细胞。结果发现,中间普氏菌脂多糖可在无额外刺激的情况下诱导分化的THP-1细胞中TNF-α mRNA表达并刺激TNF-α释放。用中间普氏菌脂多糖处理细胞导致三种MAPK [细胞外信号相关激酶1/2(ERK1/2)、c-Jun氨基末端激酶1/2(JNK1/2)和p38]同时激活。用MAPK抑制剂预处理细胞可有效抑制中间普氏菌脂多糖诱导的TNF-α产生,而不影响TNF-α mRNA的表达。因此,这些数据提供了充分的证据,表明MAPK信号通路在中间普氏菌脂多糖诱导的TNF-α合成的翻译水平而非转录水平的调节中是必需的。

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