Department of Oral Rehabilitation and Regenerative Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
J Bone Miner Res. 2019 Feb;34(2):327-332. doi: 10.1002/jbmr.3598. Epub 2018 Oct 23.
Bone morphogenetic protein 2 (BMP-2) is widely known as a potent growth factor that promotes bone formation. However, an increasing number of studies have demonstrated side effects of BMP-2 therapy. A deeper understanding of the effect of BMP-2 on cells other than those involved directly in bone remodeling is of fundamental importance to promote a more effective delivery of BMP-2 to patients. In this study, we aimed to investigate the effect of BMP-2 in the marrow environment. First, BMP-2 adsorbed onto titanium implants was delivered at the tooth extraction socket (marrow-absent site) or in the mandible marrow of beagle dogs. BMP-2 could induce marked bone formation around the implant at the tooth extraction socket. Surprisingly, however, no bone formation was observed in the BMP-2-coated titanium implants inserted in the mandible marrow. In C57BL/6 mice, BMP-2 adsorbed in freeze-dried collagen pellets could induce bone formation in marrow-absent calvarial bone. However, similar to the canine model, BMP-2 could not induce bone formation in the femur marrow. Analysis of osteoblast differentiation using Col1a1(2.3)-GFP transgenic mice revealed a scarce number of osteoblasts in BMP-2-treated femurs, whereas in the control group, osteoblasts were abundant. Ablation of femur marrow recovered the BMP-2 ability to induce bone formation. In vitro experiments analyzing luciferase activity of C2C12 cells with the BMP-responsive element and alkaline phosphatase activity of MC3T3-E1 osteoblasts further revealed that bone marrow cells inhibit the BMP-2 effect on osteoblasts by direct cell-cell contact. Collectively, these results showed that the effect of BMP-2 in inducing bone formation is remarkably repressed by marrow cells via direct cell-cell contact with osteoblasts; this opens new perspectives on the clarification of the side-effects associated with BMP-2 application. © 2018 American Society for Bone and Mineral Research.
骨形态发生蛋白 2(BMP-2)是一种广泛熟知的促骨形成的强力生长因子。然而,越来越多的研究表明 BMP-2 治疗存在副作用。更深入地了解 BMP-2 对除直接参与骨重塑的细胞以外的细胞的影响,对于更有效地将 BMP-2 递送给患者至关重要。在这项研究中,我们旨在研究 BMP-2 在骨髓环境中的作用。首先,将吸附在钛植入物上的 BMP-2 递送至拔牙窝(无骨髓部位)或比格犬下颌骨骨髓中。BMP-2 可在拔牙窝中的植入物周围诱导明显的骨形成。然而,令人惊讶的是,在插入下颌骨骨髓的 BMP-2 涂层钛植入物中未观察到骨形成。在 C57BL/6 小鼠中,吸附在冻干胶原微球中的 BMP-2 可在无骨髓的颅盖骨中诱导骨形成。然而,与犬模型相似,BMP-2 不能诱导股骨骨髓中的骨形成。使用 Col1a1(2.3)-GFP 转基因小鼠分析成骨细胞分化的结果显示,BMP-2 处理的股骨中成骨细胞数量稀少,而在对照组中,成骨细胞丰富。股骨骨髓的消融恢复了 BMP-2 诱导骨形成的能力。体外实验分析具有 BMP 反应元件的 C2C12 细胞的荧光素酶活性和 MC3T3-E1 成骨细胞的碱性磷酸酶活性进一步表明,骨髓细胞通过直接细胞-细胞接触抑制 BMP-2 对成骨细胞的作用。总之,这些结果表明,骨髓细胞通过与成骨细胞的直接细胞-细胞接触,显著抑制 BMP-2 诱导骨形成的作用;这为阐明 BMP-2 应用相关的副作用提供了新的视角。 © 2018 美国骨与矿物质研究学会。