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首页> 外文期刊>Journal of biomedical materials research, Part A >Pro-osteoclastic in vitro effect of Polyethylene-like nanoparticles: Involvement in the pathogenesis of implant aseptic loosening
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Pro-osteoclastic in vitro effect of Polyethylene-like nanoparticles: Involvement in the pathogenesis of implant aseptic loosening

机译:聚乙烯样纳米颗粒的破骨细胞的体外破骨作用:参与植入物无菌性松动的发病机理

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摘要

Polyethylene micro-sized wear particles released from orthopedic implants promote inflammation and osteolysis; however, less is known about the bioactivity of polyethylene nanosized wear particles released from the last generation of polymer-bearing surfaces. We aim to assess the internalization of fluorescent polyethylene-like nanoparticles by both human macrophages and osteoclasts and also, to determine their effects in osteoclastogenesis in vitro. Human macrophages and osteoclasts were incubated with several ratios of fluorescent polyethylene-like nanoparticles between 1 and 72 h, and 4 h, 2, 4, 6, and 9 days, respectively. The internalization of nanoparticles was quantified by flow cytometry and followed by both confocal and video time-lapse microscopy. Osteoclast differentiation and activity was semiquantified by tartrate-resistant acid phosphatase (TRAP) staining, TRAP mRNA relative expression, and pit resorption assay, respectively. Macrophages, osteoclast precursors and mature osteoclasts internalized nanoparticles in a dose-and time-dependent manner and maintained their resorptive activity. In addition, nanoparticles significantly increased the osteoclastogenesis as shown by upregulation of the TRAP expressing cell number. We conclude that polyethylene-like nanosized wear particles promote osteoclast differentiation without alteration of bone resorptive activity of mature osteoclasts and they could be considered as important actors in periprosthetic osteolysis of the last new generation of polymer-bearing surfaces. (C) 2016 Wiley Periodicals, Inc.
机译:骨科植入物释放出的聚乙烯微细磨损颗粒会促进炎症和骨溶解。然而,从最后一代的含聚合物表面释放的聚乙烯纳米尺寸磨损颗粒的生物活性知之甚少。我们旨在评估人类巨噬细胞和破骨细胞对荧光聚乙烯样纳米颗粒的内在化,并确定其在体外破骨细胞形成中的作用。将人巨噬细胞和破骨细胞分别与几种比例的荧光聚乙烯样纳米颗粒孵育1至72小时,以及4小时,2、4、6和9天。纳米颗粒的内在化通过流式细胞仪定量,然后通过共聚焦和视频延时显微镜进行定量。分别通过抗酒石酸酸性磷酸酶(TRAP)染色,TRAP mRNA相对表达和凹坑吸收测定法对破骨细胞的分化和活性进行半定量。巨噬细胞,破骨细胞前体和成熟的破骨细胞以剂量和时间依赖的方式内化了纳米颗粒,并保持了它们的吸收活性。另外,如上调TRAP表达细胞数所示,纳米颗粒显着增加了破骨细胞生成。我们得出的结论是,类似聚乙烯的纳米磨损颗粒可促进破骨细胞分化,而不会改变成熟破骨细胞的骨吸收活性,并且它们可被视为近代新一代含聚合物表面假体周围骨溶解的重要因素。 (C)2016威利期刊公司

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