Department of Orthopedics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Department of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Mol Med Rep. 2018 Jun;17(6):7746-7756. doi: 10.3892/mmr.2018.8797. Epub 2018 Mar 28.
The effect of running on bone mass depends on its intensity. However, the underlying molecular mechanism that associates running intensity with bone mass is unclear. The current study examined the effects of treadmill running at different intensities on bone mass and osteogenic differentiation of bone marrow stromal cells (BMSCs) in a rat model. A total of 24 male Wistar rats were randomly divided into groups and subjected to no running (Con group), low‑intensity running (LIR group), moderate‑intensity running (MIR group), and high‑intensity running (HIR group). Histological, immunohistochemistry and micro‑CT examinations were performed on the femora harvested after 8 weeks of treadmill running. The study demonstrated that treadmill running affected trabecular bone mass in an intensity‑dependent manner. In addition, such an intensity‑dependent effect was also demonstrated on the osteogenic and adipogenic differentiation and proliferation of BMSCs. Furthermore, the Wnt/β‑catenin signaling pathway may be involved in the running‑induced increase in bone mass in rats in the MIR group. There appears to be a biomechanical 'window', in which running‑induced strain signals can increase the number of BMSCs and progenitor cells (specific to the osteoblast lineage) causing upregulation of osteogenesis and downregulation of adipogenesis of BMSCs. This finding may provide insight into the molecular and cellular mechanisms responsible for bone homeostasis.
跑步对骨量的影响取决于其强度。然而,将跑步强度与骨量联系起来的潜在分子机制尚不清楚。本研究在大鼠模型中检查了不同强度的跑步机跑步对骨量和骨髓基质细胞(BMSC)成骨分化的影响。总共 24 只雄性 Wistar 大鼠被随机分为 4 组,分别进行不跑步(Con 组)、低强度跑步(LIR 组)、中等强度跑步(MIR 组)和高强度跑步(HIR 组)。在跑步机跑步 8 周后采集股骨进行组织学、免疫组织化学和 micro-CT 检查。研究表明,跑步机跑步以强度依赖的方式影响小梁骨量。此外,这种强度依赖性效应也表现在 BMSC 的成骨和成脂分化和增殖上。此外,Wnt/β-catenin 信号通路可能参与了 MIR 组大鼠跑步引起的骨量增加。似乎存在一个生物力学“窗口”,在这个窗口中,跑步引起的应变信号可以增加 BMSC 和祖细胞(特定于成骨细胞谱系)的数量,导致 BMSC 成骨增加和成脂减少。这一发现可能为骨稳态的分子和细胞机制提供了新的见解。