Jing Da, Tong Shichao, Zhai Mingming, Li Xiaokang, Cai Jing, Wu Yan, Shen Guanghao, Zhang Xuhui, Xu Qiaoling, Guo Zheng, Luo Erping
Department of Biomedical Engineering, Fourth Military Medical University, Xi'an, China.
Institute of Orthopaedics, Xijing hospital, Fourth Military Medical University, Xi'an, China.
Sci Rep. 2015 Nov 25;5:17134. doi: 10.1038/srep17134.
Emerging evidence substantiates the potential of porous titanium alloy (pTi) as an ideal bone-graft substitute because of its excellent biocompatibility and structural properties. However, it remains a major clinical concern for promoting high-efficiency and high-quality osseointegration of pTi, which is beneficial for securing long-term implant stability. Accumulating evidence demonstrates the capacity of low-amplitude whole-body vibration (WBV) in preventing osteopenia, whereas the effects and mechanisms of WBV on osteogenesis and osseointegration of pTi remain unclear. Our present study shows that WBV enhanced cellular attachment and proliferation, and induced well-organized cytoskeleton of primary osteoblasts in pTi. WBV upregulated osteogenesis-associated gene and protein expression in primary osteoblasts, including OCN, Runx2, Wnt3a, Lrp6 and β-catenin. In vivo findings demonstrate that 6-week and 12-week WBV stimulated osseointegration, bone ingrowth and bone formation rate of pTi in rabbit femoral bone defects via μCT, histological and histomorphometric analyses. WBV induced higher ALP, OCN, Runx2, BMP2, Wnt3a, Lrp6 and β-catenin, and lower Sost and RANKL/OPG gene expression in rabbit femora. Our findings demonstrate that WBV promotes osteogenesis and osseointegration of pTi via its anabolic effect and potential anti-catabolic activity, and imply the promising potential of WBV for enhancing the repair efficiency and quality of pTi in osseous defects.
新出现的证据证实了多孔钛合金(pTi)作为理想骨移植替代物的潜力,因为它具有出色的生物相容性和结构特性。然而,促进pTi高效、高质量的骨整合仍是一个主要的临床问题,而骨整合有利于确保植入物的长期稳定性。越来越多的证据表明低振幅全身振动(WBV)具有预防骨质减少的能力,而WBV对pTi骨生成和骨整合的影响及机制仍不清楚。我们目前的研究表明,WBV增强了细胞附着和增殖,并诱导了pTi中原代成骨细胞有序的细胞骨架形成。WBV上调了原代成骨细胞中与骨生成相关的基因和蛋白表达,包括骨钙素(OCN)、Runx2、Wnt3a、低密度脂蛋白受体相关蛋白6(Lrp6)和β-连环蛋白。体内研究结果表明,通过显微计算机断层扫描(μCT)、组织学和组织形态计量学分析,6周和12周的WBV刺激了兔股骨骨缺损中pTi的骨整合、骨长入和骨形成率。WBV诱导兔股骨中碱性磷酸酶(ALP)、OCN、Runx2、骨形态发生蛋白2(BMP2)、Wnt3a、Lrp6和β-连环蛋白表达升高,而硬化蛋白(Sost)和核因子κB受体活化因子配体/骨保护素(RANKL/OPG)基因表达降低。我们的研究结果表明,WBV通过其合成代谢作用和潜在的抗分解代谢活性促进pTi的骨生成和骨整合,并暗示WBV在提高骨缺损中pTi修复效率和质量方面具有广阔的潜力。