Department of Anatomy and Cell Biology, Rush University Medical Center, Chicago, IL 60612, USA.
Ultrasonics. 2011 Apr;51(3):281-8. doi: 10.1016/j.ultras.2010.09.004. Epub 2010 Sep 26.
Bone growth and repair are under the control of biochemical and mechanical signals. Low-intensity pulsed ultrasound (LIPUS) stimulation at 30mW/cm(2) is an established, widely used and FDA approved intervention for accelerating bone healing in fractures and non-unions. Although this LIPUS signal accelerates mineralization and bone regeneration, the actual intensity experienced by the cells at the target site might be lower, due to the possible attenuation caused by the overlying soft tissue. The aim of this study was to investigate whether LIPUS intensities below 30mW/cm(2) are able to provoke phenotypic responses in bone cells. Rat bone marrow stromal cells were cultured under defined conditions and the effect of 2, 15, 30mW/cm(2) and sham treatments were studied at early (cell activation), middle (differentiation into osteogenic cells) and late (biological mineralization) stages of osteogenic differentiation. We observed that not only 30mW/cm(2) but also 2 and 15mW/cm(2), modulated ERK1/2 and p38 intracellular signaling pathways as compared to the sham treatment. After 5 days with daily treatments of 2, 15 and 30mW/cm(2), alkaline phosphatase activity, an early indicator of osteoblast differentiation, increased by 79%, 147% and 209%, respectively, compared to sham, indicating that various intensities of LIPUS were able to initiate osteogenic differentiation. While all LIPUS treatments showed higher mineralization, interestingly, the highest increase of 225% was observed in cells treated with 2mW/cm(2). As the intensity increased to 15 and 30mW/cm(2), the increase in the level of mineralization dropped to 120% and 82%. Our data show that LIPUS intensities lower than the current clinical standard have a positive effect on osteogenic differentiation of rat bone marrow stromal cells. Although Exogen™ at 30mW/cm(2) continues to be effective and should be used as a clinical therapy for fracture healing, if confirmed in vivo, the increased mineralization at lower intensities might be the first step towards redefining the most effective LIPUS intensity for clinical use.
骨骼的生长和修复受生化和机械信号的控制。低强度脉冲超声(LIPUS)刺激强度为 30mW/cm²是一种已确立的、广泛使用的、获得 FDA 批准的干预手段,可加速骨折和骨不连的骨愈合。尽管这种 LIPUS 信号可以加速矿化和骨再生,但由于可能由于覆盖的软组织造成的衰减,细胞在目标部位实际感受到的强度可能更低。本研究旨在探讨低于 30mW/cm²的 LIPUS 强度是否能够引起骨细胞的表型反应。大鼠骨髓基质细胞在特定条件下培养,并在成骨分化的早期(细胞激活)、中期(分化为成骨细胞)和晚期(生物矿化)阶段研究 2、15、30mW/cm²和假处理的影响。我们观察到,不仅 30mW/cm²,而且 2 和 15mW/cm²与假处理相比,还调节了 ERK1/2 和 p38 细胞内信号通路。在每天用 2、15 和 30mW/cm² 处理 5 天后,碱性磷酸酶活性,成骨细胞分化的早期指标,分别比假处理组增加了 79%、147%和 209%,表明不同强度的 LIPUS 都能够启动成骨分化。虽然所有 LIPUS 处理均显示出更高的矿化,但有趣的是,在 2mW/cm² 处理的细胞中观察到最高增加了 225%。随着强度增加到 15 和 30mW/cm²,矿化水平的增加下降到 120%和 82%。我们的数据表明,低于当前临床标准的 LIPUS 强度对大鼠骨髓基质细胞的成骨分化有积极影响。虽然 Exogen™ 30mW/cm² 仍然是有效的,应该作为骨折愈合的临床治疗方法,但如果在体内得到证实,较低强度下增加的矿化可能是重新定义最有效 LIPUS 强度用于临床应用的第一步。