Low-intensity pulsed ultrasound stimulates a bone-forming response in UMR-106 cells

被引:131
作者
Warden, SJ
Favaloro, JM
Bennell, KL [1 ]
McMeeken, JM
Ng, KW
Zajac, JD
Wark, JD
机构
[1] Univ Melbourne, Sch Physiotherapy, Ctr Sports Med Res & Educ, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Austin & Repatriat Med Ctr, Dept Med, Melbourne, Vic 3010, Australia
[4] St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
[5] Royal Melbourne Hosp, Bone & Mineral Serv, Melbourne, Vic, Australia
基金
澳大利亚研究理事会;
关键词
fracture healing; mechanical loading; mechanotransduction; RT-PCR; ultrasound therapy; UMR-106; cells;
D O I
10.1006/bbrc.2001.5412
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Low-intensity (<100 mW/cm(2)) pulsed ultrasound (US) is an established therapy for fracture repair. In both animal and human trials, such US has been shown to facilitate fresh fracture repair and initiate healing in fractures with repair defects. However, the mechanism by which US achieves these outcomes is not clear. One possible mechanism is the direct stimulation of bone formation. To investigate this hypothesis, the current study investigated the mRNA response of isolated bone-forming cells (UMR-106 cells) to a single 20-min dose of low-intensity pulsed US. Using a novel US-cell coupling method, US was found to stimulate expression of the immediate-early response genes c-fos and COX-2 and elevate mRNA levels for the bone matrix proteins ALP and OC. These findings suggest that low-intensity pulsed US has a direct effect on bone formation. This may contribute to the beneficial effect of low-intensity pulsed US on fracture repair. (C) 2001 Academic Press.
引用
收藏
页码:443 / 450
页数:8
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