Dept. of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-5281, United States.
Dept. of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-5281, United States.
Arch Biochem Biophys. 2014 Mar 1;545:154-61. doi: 10.1016/j.abb.2014.01.021. Epub 2014 Jan 30.
Recently we have developed a dynamic hydraulic stimulation (DHS) as a loading modality to induce anabolic responses in bone. To further study the functional process of DHS regulated bone metabolism, the objective of this study was to evaluate the effects of DHS on cortical bone and its alterations on gene expressions of osteogenic growth factors and transcription factors as a function of time. Using a model system of 5-month-old hindlimb suspended (HLS) female Sprague-Dawley rats, DHS was applied to the right tibiae of the stimulated rats with a loading frequency of 2Hz with 30mmHg (p-p) dynamic pressure, 5days/week, for a total of 28days. Midshafts of the tibiae were analyzed using μCT and histology. Total RNA was analyzed using RT-PCR on selected osteogenic genes (RUNX2, β-catenin, osteopontin, VEGF, BMP2, IGF-1, and TGF-β) on 3-, 7-, 14- , and 21-day. Results showed increased Cort.Th and Ct.BV/TV as well as a time-dependent fashion of gradual changes in mRNA levels upon DHS. While DHS-driven fold changes of the mRNA levels remained low before Day-7, its fold changes started to elevate by Day-14 and then dropped by Day-21. This study further delineates the underlying molecular mechanism of DHS-derived mechanical signals, and its time-dependent optimization.
最近,我们开发了一种动态液压刺激(DHS)作为加载方式,以诱导骨骼中的合成代谢反应。为了进一步研究 DHS 调节骨代谢的功能过程,本研究旨在评估 DHS 对皮质骨的影响及其对成骨生长因子和转录因子基因表达的改变随时间的变化。使用 5 月龄后肢悬吊(HLS)雌性 Sprague-Dawley 大鼠的模型系统,以 2Hz 的加载频率对刺激大鼠的右侧胫骨施加 DHS,动态压力为 30mmHg(p-p),每周 5 天,共 28 天。使用 μCT 和组织学分析胫骨中段。在第 3、7、14 和 21 天时,使用 RT-PCR 分析选定的成骨基因(RUNX2、β-catenin、骨桥蛋白、VEGF、BMP2、IGF-1 和 TGF-β)的总 RNA。结果显示,Cort.Th 和 Ct.BV/TV 增加,以及 DHS 后 mRNA 水平呈时间依赖性的逐渐变化。虽然 DHS 驱动的 mRNA 水平的倍数变化在第-7 天之前仍然较低,但从第-14 天开始,其倍数变化开始升高,然后在第-21 天下降。本研究进一步阐述了 DHS 衍生的机械信号及其时间依赖性优化的潜在分子机制。