Department of Restorative Dentistry and Biomaterials, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Antimicrob Agents Chemother. 2012 Jul;56(7):3776-84. doi: 10.1128/AAC.00114-12. Epub 2012 May 7.
In this study, we aimed to establish an in vitro bacterium/bone cell coculture model system and to use this model for dose dependence studies of dual administration of antibiotics and growth factors in vitro. We examined the effect of single or dual administration of the antibiotic vancomycin (VAN) at 0 to 16 μg/ml and bone morphogenetic protein-2 (BMP-2) at 0 or 100 ng/ml on both methicillin-sensitive Staphylococcus aureus and mouse bone marrow stromal cells (W-20-17) under both mono- and coculture conditions. Cell metabolic activity, Live/Dead staining, double-stranded DNA (dsDNA) amounts, and alkaline phosphatase activity were measured to assess cell viability, proliferation, and differentiation. An interleukin-6 (IL-6) enzyme-linked immunosorbent assay (ELISA) kit was used to test the bone cell inflammation response in the presence of bacteria. Our results suggest that, when delivered together in coculture, VAN and BMP-2 maintain their primary functions as an antibiotic and a growth factor, respectively. Most interestingly, this dual-delivery type of approach has shown itself to be effective at lower concentrations of VAN than those required for an approach relying strictly on the antibiotic. It may be that BMP-2 enhances cell proliferation and differentiation before the cells become infected. In coculture, a dosage of VAN higher than that used for treatment in monoculture may be necessary to effectively inhibit growth of Staphylococcus aureus. This could mean that the coculture environment may be limiting the efficacy of VAN, possibly by way of bacterial invasion of the bone cells. This report of a coculture study demonstrates a potential beneficial effect of the coadministration of antibiotics and growth factors compared to treatment with antibiotic alone.
在这项研究中,我们旨在建立一种体外细菌/骨细胞共培养模型系统,并使用该模型进行抗生素和生长因子双重给药的体外剂量依赖性研究。我们研究了在单核和共培养条件下,单独或联合给予抗生素万古霉素(VAN)0 至 16 μg/ml 和骨形态发生蛋白-2(BMP-2)0 或 100 ng/ml 对耐甲氧西林金黄色葡萄球菌和小鼠骨髓基质细胞(W-20-17)的影响。通过测量细胞代谢活性、Live/Dead 染色、双链 DNA(dsDNA)量和碱性磷酸酶活性来评估细胞活力、增殖和分化。使用白细胞介素-6(IL-6)酶联免疫吸附测定(ELISA)试剂盒检测细菌存在时骨细胞的炎症反应。我们的结果表明,在共培养中联合给药时,VAN 和 BMP-2 分别保持其作为抗生素和生长因子的主要功能。最有趣的是,与严格依赖抗生素的方法相比,这种双重给药方式在较低浓度的 VAN 下显示出有效性。可能是 BMP-2 在细胞感染之前增强了细胞增殖和分化。在共培养中,可能需要高于单核培养中用于治疗的万古霉素剂量来有效抑制金黄色葡萄球菌的生长。这可能意味着共培养环境可能会限制 VAN 的疗效,可能是通过细菌侵入骨细胞。本共培养研究报告表明,与单独使用抗生素相比,抗生素和生长因子的联合给药可能具有潜在的有益效果。