首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Quantitative analysis of osteoclast-specific gene markers stimulated by lipopolysaccharide.
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Quantitative analysis of osteoclast-specific gene markers stimulated by lipopolysaccharide.

机译:脂多糖刺激破骨细胞特异性基因标记的定量分析。

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摘要

Lipopolysaccharide (LPS) in the outer layers of Gram-negative bacteria plays an important role in initiating and sustaining periapical lesions. To understand the mechanisms of osteoclastic bone resorption in periapical lesions induced by LPS, we stimulated osteoclast precursors, RAW 264.7 cells with LPS. LPS stimulated osteoclastogenesis when osteoclast precursors were primed with activator for NF-kappaB ligand (RANKL) as little as 24 h. By employing real-time PCR analysis, we have confirmed that osteoclast-like cells stimulated by LPS express high level of osteoclast-specific gene markers such as TRAP, cathepsin K, and calcitonin receptor. These results suggest that bone-resportive action by LPS is partially independent of RANKL.
机译:革兰氏阴性细菌外层的脂多糖(LPS)在引发和维持根尖周病变中起着重要作用。为了了解LPS诱导的根尖周病变中破骨细胞骨吸收的机制,我们用LPS刺激破骨细胞前体RAW 264.7细胞。当破骨细胞前体用活化剂激活NF-κB配体(RANKL)最少24小时时,LPS刺激破骨细胞生成。通过使用实时PCR分析,我们已经证实,LPS刺激的破骨细胞样细胞表达高水平的破骨细胞特异性基因标记,如TRAP,组织蛋白酶K和降钙素受体。这些结果表明,LPS的骨传导作用部分独立于RANKL。

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