骨愈合
间充质干细胞
医学
骨矿物
离体
骨质疏松症
化学
体内
内科学
泌尿科
生物医学工程
外科
病理
生物
生物技术
作者
F-Y Wei,Simon Kwoon‐Ho Chow,K. S. Leung,Min Qin,Anyun Guo,OL Yu,Gang Li,Wing‐Hoi Cheung
摘要
Low-magnitude high-frequency vibration (LMHFV) has been proven to promote osteoporotic fracture healing.Mechanical stimulation was reported to enhance SDF-1/ CXCR4 signalling in mesenchymal stem cells (MSCs).We hypothesised that LMHFV promoted osteoporotic fracture healing by enhancing MSC migration through the SDF-1/ CXCR4 pathway.152 ovariectomised SD-rats received closed femoral fracture in groups of vibration+MSC (VMG) (20 min/d, 5 d/week), vibration+MSC+AMD3100 (VMAG; AMD, a CXCR4 inhibitor) (1 mg/kg/d, intraperitoneal), MSC (MG) (1 × 10 6 MSC, intracardiac) or control (CG) for a treatment duration of 2, 4 or 8 weeks.MSC migration was evaluated by ex-vivo green fluorescent protein signal in the callus; and fracture healing was examined by weekly radiographs, endpoint computedtomography and mechanical test.At week-2 and week-4, ex-vivo callus GFP intensity of VMG was significantly higher than other groups (p < 0.05).From week-2 to week-3, both callus width and callus area in VMG were significantly larger; and from week-7 to week-8, smaller than other groups (p < 0.05).At week-8, high-density bone volume fraction, bone volume fraction, bone mineral density and stiffness in VMG were significantly higher than other 3 groups (p < 0.05).This study demonstrated that LMHFV promoted MSC migration and fracture healing in osteoporotic rats.This effect was attenuated by CXCR4 inhibitor, providing strong evidence that SDF-1-mediated MSC migration was one of the important mechanisms through which LMHFV enhanced fracture healing.
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