Remmers Stefan J A, van der Heijden Freek C, 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 21;18:101651. doi: 10.1016/j.bonr.2022.101651. eCollection 2023 Jun.
The bone resorbing osteoclasts are a complex type of cell essential for bone remodeling. There is no consensus on medium composition and seeding density for osteoclastogenesis, despite the importance thereof on osteoclastic differentiation and activity. The aim of this study was to investigate the relative effect of monocyte or peripheral blood mononuclear cell (PBMC) seeding density, osteoclastic supplement concentration and priming on the generation of functional osteoclasts, and to explore and evaluate the usefulness of commonly used markers for osteoclast cultures. Morphology and osteoclast formation were analyzed with fluorescence imaging for tartrate resistant acid phosphatase (TRAP) and integrin β3 (Iβ3). TRAP release was analyzed from supernatant samples, and resorption was analyzed from culture on Corning® Osteo Assay plates. In this study, we have shown that common non-standardized culturing conditions of monocyte or PBMCs had a significant effect on the generation of functional osteoclasts. We showed how increased osteoclastic supplement concentrations supported osteoclastic differentiation and resorption but not TRAP release, while priming resulted in increased TRAP release as well. Increased monocyte seeding densities resulted in more and large TRAP positive bi-nuclear cells, but not directly in more multinucleated osteoclasts, resorption or TRAP release. Increasing PBMC seeding densities resulted in more and larger osteoclasts and more resorption, although resorption was disproportionally low compared to the monocyte seeding density experiment. Exploration of commonly used markers for osteoclast cultures demonstrated that Iβ3 staining was an excellent and specific osteoclast marker in addition to TRAP staining, while supernatant TRAP measurements could not accurately predict osteoclastic resorptive activity. With improved understanding of the effect of seeding density and osteoclastic supplement concentration on osteoclasts, experiments yielding higher numbers of functional osteoclasts can ultimately improve our knowledge of osteoclasts, osteoclastogenesis, bone remodeling and bone diseases.
骨吸收破骨细胞是骨重塑所必需的一种复杂细胞类型。尽管破骨细胞生成的培养基成分和接种密度对破骨细胞分化和活性很重要,但目前尚无共识。本研究的目的是探讨单核细胞或外周血单个核细胞(PBMC)接种密度、破骨细胞补充剂浓度和预刺激对功能性破骨细胞生成的相对影响,并探索和评估破骨细胞培养常用标志物的实用性。通过对耐酒石酸酸性磷酸酶(TRAP)和整合素β3(Iβ3)进行荧光成像分析形态和破骨细胞形成。从上清液样本中分析TRAP释放,并在康宁®骨分析板上培养分析骨吸收。在本研究中,我们表明单核细胞或PBMC常见的非标准化培养条件对功能性破骨细胞的生成有显著影响。我们展示了增加破骨细胞补充剂浓度如何支持破骨细胞分化和骨吸收,但不支持TRAP释放,而预刺激也导致TRAP释放增加。单核细胞接种密度增加导致更多且更大的TRAP阳性双核细胞,但并未直接导致更多的多核破骨细胞、骨吸收或TRAP释放。增加PBMC接种密度导致更多且更大的破骨细胞和更多的骨吸收,尽管与单核细胞接种密度实验相比,骨吸收低得不成比例。对破骨细胞培养常用标志物的探索表明,除TRAP染色外,Iβ3染色是一种优秀且特异的破骨细胞标志物,而上清液TRAP测量不能准确预测破骨细胞的吸收活性。随着对接种密度和破骨细胞补充剂浓度对破骨细胞影响的认识加深,产生更多功能性破骨细胞的实验最终可以增进我们对破骨细胞、破骨细胞生成、骨重塑和骨疾病的了解。