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Mesenchymal stem cell sheet transplantation combined with locally released simvastatin enhances bone formation in a rat tibia osteotomy model

机译:间充质干细胞表皮移植结合局部释放的辛伐他汀可增强大鼠胫骨截骨模型的骨形成

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Nonunion of fractured bones is a common clinical problem for orthopedic surgeons. This study aimed to investigate the effects of simvastatin locally applied from calcium sulfate (CS) combined with a mesenchymal stem cell (MSC) sheet on fracture healing. In vitro, the proliferation and differentiation of rat bone marrowederived MSCs stimulated by simvastatin were investigated. In vivo, an osteotomy model was made in rat tibia, and fractured tibias were treated with CS, CS/ simvastatin, CS/MSC sheet or simvastatin-loaded CS with MSC or untreated (control). Tibias were harvested at 2 or 8 weeks and underwent real-time quantitative polymerase chain reaction, x-ray, micro-CT and histological analysis. The expression levels of bone morphogenetic protein 2, alkaline phosphatase, osteocalcin, osteoprotegerin and vascular endothelial growth factor of simvastatin-induced MSCs increased with the concentrations of the simvastatin, significantly higher than those in the MSCs group. At 2 weeks, the CS/simvastatin/MSC sheet group showed significantly higher expressions of bone morphogenetic protein 2, alkaline phosphatase, osteocalcin, osteoprotegerin and vascular endothelial growth factor, with more callus formation around the fracture site compared with the other four groups. At 8 weeks, complete bone union was obtained in the CS/simvastatin/MSC sheet group. By contrast, newly regenerated bone tissue partially bridged the gap in the CS/simvastatin group and the CS/MSC sheet group; the control and CS group showed nonunion of the tibia. These results show that both simvastatin and the MSC sheet contributed to the formation of new bone and that the tibia fracture was completely healed by transplantation of the MSC sheet with locally applied simvastatin. Such MSC sheet with locally applied simvastatin might contribute to the treatment of fractures, bone delayed unions or nonunions in clinical practice.
机译:对于整形外科医生来说,骨折的骨不连是常见的临床问题。这项研究旨在调查从硫酸钙(CS)局部施用的辛伐他汀联合间充质干细胞(MSC)片对骨折愈合的影响。在体外,研究了辛伐他汀刺激的大鼠骨髓间充质干细胞的增殖和分化。在体内,在大鼠胫骨中制成截骨模型,并用CS,CS /辛伐他汀,CS / MSC片或用MSC加载辛伐他汀的CS或未经治疗(对照)治疗胫骨骨折。在第2周或第8周收获胫骨,并进行实时定量聚合酶链反应,X射线,显微CT和组织学分析。辛伐他汀诱导的MSCs骨形态发生蛋白2,碱性磷酸酶,骨钙素,骨保护素和血管内皮生长因子的表达水平随辛伐他汀的浓度而升高,明显高于MSCs组。在第2周,CS /辛伐他汀/ MSC片组显示出骨形态发生蛋白2,碱性磷酸酶,骨钙素,骨保护素和血管内皮生长因子的表达明显较高,与其他四组相比,骨折部位周围的愈伤组织形成更多。在第8周,CS /辛伐他汀/ MSC片组获得了完全的骨结合。相反,新近再生的骨组织部分弥合了CS /辛伐他汀组和CS / MSC片组中的间隙。对照组和CS组显示胫骨骨不连。这些结果表明,辛伐他汀和MSC片均有助于新骨的形成,并且通过将MSC片与局部应用的辛伐他汀进行移植,胫骨骨折得以完全治愈。具有局部应用辛伐他汀的这种MSC片在临床实践中可能有助于骨折,骨延迟性愈合或骨不连的治疗。

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