Remmers Stefan J A, van der Heijden Freek C, de Wildt Bregje W M, Ito Keita, Hofmann Sandra
Orthopaedic Biomechanics, Department of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, the Netherlands.
Bone Rep. 2022 Dec 12;18:101646. doi: 10.1016/j.bonr.2022.101646. eCollection 2023 Jun.
The aim of the present study was to further improve an 3D osteoblast (OB) - osteoclast (OC) co-culture model of bone by tuning it towards states of formation, resorption, and equilibrium for their future applications in fundamental research, drug development and personalized medicine. This was achieved by varying culture medium composition and monocyte seeding density, the two external parameters that affect cell behavior the most. Monocytes were seeded at two seeding densities onto 3D silk-fibroin constructs pre-mineralized by MSC-derived OBs and were co-cultured in one of three different media (OC stimulating, Neutral and OB stimulating medium) for three weeks. Histology showed mineralized matrix after co-culture and OC markers in the OC medium group. Scanning Electron Microscopy showed large OC-like cells in the OC medium group. Micro-computed tomography showed increased formation in the OB medium group, equilibrium in the Neutral medium group and resorption in the OC medium group. Culture supernatant samples showed high early tartrate resistant acid phosphatase (TRAP) release in the OC medium group, a later and lower release in the Neutral medium group, and almost no release in the OB medium group. Increased monocyte seeding density showed a less-than-proportional increase in TRAP release and resorption in OC medium, while it proportionally increased TRAP release in Neutral medium without affecting net resorption. The 3D OB-OC co-culture model was effectively used to show an excess of mineral deposition using OB medium, resorption using OC medium, or an equilibrium using Neutral medium. All three media applied to the model may have their own distinct applications in fundamental research, drug development, and personalized medicine.
本研究的目的是进一步改进一种三维成骨细胞(OB)-破骨细胞(OC)骨共培养模型,通过将其调整为形成、吸收和平衡状态,以便在基础研究、药物开发和个性化医疗中得到应用。这是通过改变培养基成分和单核细胞接种密度这两个对细胞行为影响最大的外部参数来实现的。将单核细胞以两种接种密度接种到由间充质干细胞衍生的成骨细胞预矿化的三维丝素蛋白构建体上,并在三种不同培养基(破骨细胞刺激培养基、中性培养基和成骨细胞刺激培养基)之一中共同培养三周。组织学显示共培养后有矿化基质,且破骨细胞培养基组中有破骨细胞标志物。扫描电子显微镜显示破骨细胞培养基组中有大型破骨细胞样细胞。显微计算机断层扫描显示成骨细胞培养基组形成增加,中性培养基组处于平衡状态,破骨细胞培养基组有吸收。培养上清液样本显示破骨细胞培养基组早期抗酒石酸酸性磷酸酶(TRAP)释放量高,中性培养基组释放较晚且量较低,而成骨细胞培养基组几乎无释放。增加单核细胞接种密度显示,在破骨细胞培养基中TRAP释放和吸收的增加低于比例增加,而在中性培养基中TRAP释放按比例增加且不影响净吸收。三维成骨细胞-破骨细胞共培养模型有效地用于显示使用成骨细胞培养基时矿物质沉积过多、使用破骨细胞培养基时的吸收或使用中性培养基时的平衡。应用于该模型的所有三种培养基在基础研究、药物开发和个性化医疗中可能都有各自独特的应用。