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Mechanisms of Staphylococcus aureus invasion of cultured osteoblasts

机译:金黄色葡萄球菌入侵培养成骨细胞的机制

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摘要

Staphylococcus aureus is a bacterial pathogen causing approximately 80% of all cases of human osteomyelitis. This bacterium can adhere to and become internalized by osteoblasts and previous studies indicate that osteoblasts are active in the internalization process. In the current study, we examined the roles of microfilaments, microtubules and clathrin-dependent receptor-mediated endocytosis in the internalization of S. aureus by MC3T3-E1 mouse osteoblast cells. Microfilament and microtubule polymerization was inhibited with cytochalasin D and colchicine. Clathrin-coated pit formation was examined by using the transaminase inhibitor, monodanslycadaverine. The results of this study indicate that mouse osteoblasts utilize actin microfilaments, microtubules and clathrin-coated pits in the internalization of S. aureus; however, microfilaments seem to play the most significant role in the invasion process.
机译:金黄色葡萄球菌是一种细菌性病原体,可引起约80%的人类骨髓炎病例。该细菌可以粘附并被成骨细胞内化,先前的研究表明成骨细胞在内化过程中具有活性。在当前的研究中,我们检查了微丝,微管和网格蛋白依赖性受体介导的内吞作用在MC3T3-E1小鼠成骨细胞内在金黄色葡萄球菌内化中的作用。细胞松弛素D和秋水仙碱抑制微丝和微管聚合。通过使用转氨酶抑制剂monodanslycadaverine检查网格蛋白涂层的凹坑形成。这项研究的结果表明,小鼠成骨细胞在金黄色葡萄球菌的内在化过程中利用肌动蛋白微丝,微管和网格蛋白包被的凹坑。然而,微丝似乎在入侵过程中起着最重要的作用。

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