Buizer Arina T, Veldhuizen Albert G, Bulstra Sjoerd K, Kuijer Roel
Department of Orthopaedic Surgery, University of Groningen, University Medical Centre Groningen, The Netherlands Department of Biomedical Engineering, University of Groningen, University Medical Centre Groningen, The Netherlands.
Department of Orthopaedic Surgery, University of Groningen, University Medical Centre Groningen, The Netherlands.
J Biomater Appl. 2014 Jul;29(1):3-13. doi: 10.1177/0885328213512171. Epub 2013 Dec 10.
An adequate cell seeding technique is essential for effective bone regeneration on cell seeded constructs of porous tricalcium phosphates. In previous studies, dynamic cell seeding, in which an external force is applied to seed cells on a biomaterial, resulted in more homogeneous cell seeding in low porosity scaffolds than static seeding. The optimal cell seeding technique for high porosity scaffolds has not been defined yet. Human mesenchymal stem cells were isolated from bone marrow and characterized. The cells were seeded on low porosity (45%) and high porosity (90%) tricalcium phosphate scaffolds using a static and a vacuum seeding technique. LIVE/DEAD® staining of the cell-scaffold complexes followed by confocal laser scanning microscopy was used to measure cell proliferation, cell distribution and cell viability one, three and seven days after seeding. Cell proliferation was also quantified using a DNA quantification assay. Neither static nor vacuum seeding resulted in homogeneous cell seeding on both low and high porosity scaffolds. Cell density was lower on the inside than on the outside of the scaffolds. On low porosity scaffolds, the vacuum method yielded the highest numbers of cells compared to the static method. Low porosity scaffolds were seeded most homogeneously using the static seeding method. Seven days after seeding, numbers of adherent cells were comparable for both scaffold types and independent of the cell seeding technique used. In conclusion, on high porosity scaffolds, static seeding results in more homogeneous cell seeding and it is easier to use than a vacuum seeding technique.
一种合适的细胞接种技术对于在多孔磷酸三钙细胞接种构建体上实现有效的骨再生至关重要。在先前的研究中,动态细胞接种(即在生物材料上施加外力来接种细胞)相比于静态接种,在低孔隙率支架中能产生更均匀的细胞接种效果。然而,高孔隙率支架的最佳细胞接种技术尚未明确。从骨髓中分离并鉴定了人间充质干细胞。使用静态接种技术和真空接种技术将细胞接种到低孔隙率(45%)和高孔隙率(90%)的磷酸三钙支架上。接种后1天、3天和7天,对细胞 - 支架复合物进行活/死染色,随后通过共聚焦激光扫描显微镜来测量细胞增殖、细胞分布和细胞活力。还使用DNA定量测定法对细胞增殖进行定量。无论是静态接种还是真空接种,在低孔隙率和高孔隙率支架上均未产生均匀的细胞接种效果。支架内部的细胞密度低于外部。在低孔隙率支架上,与静态接种方法相比,真空接种方法产生的细胞数量最多。使用静态接种方法在低孔隙率支架上接种的细胞最为均匀。接种7天后,两种支架类型上的贴壁细胞数量相当,且与所使用的细胞接种技术无关。总之,对于高孔隙率支架,静态接种能产生更均匀的细胞接种效果,并且比真空接种技术更易于操作。