Damaraju Swathi, Matyas John R, Rancourt Derrick E, Duncan Neil A
1 Biomedical Engineering Program, McCaig Institute for Bone and Joint Health, University of Calgary , Calgary, Alberta, Canada .
Tissue Eng Part A. 2014 Dec;20(23-24):3142-53. doi: 10.1089/ten.TEA.2014.0026.
Developing a viable and functional bone scaffold in vitro that is capable of surviving and bearing mechanical load in vivo requires an understanding of the cell biology of osteoprogenitor cells, particularly how they are influenced by mechanical stimulation during cell differentiation and maturation. In this study, mechanical load was applied using a modified FlexCell plate to impart confined compression to collagen-I scaffolds seeded with undifferentiated murine embryonic stem cells. The activity, presence, and expression of osteoblast-cadherin (OB-Cad) and connexin-43, as well as various pluripotent and osteogenic markers were examined at 5-30 days of differentiation as cells were stimulated to differentiate to osteoblasts with and without applied mechanical load. Fluorescence recovery after photobleaching, immunofluorescence, viability, von Kossa, and real-time polymerase chain reaction assessments revealed that mechanical prestimulation of this cell-seeded scaffold altered the expression of OB-Cad and connexin-43 and resulted in significant differences in the structure and organization of mineralization present in the collagen matrix. Specifically, cells in gels that were loaded for 40 h after 5 days of differentiation and then left to fully differentiate for 30 days produced a highly structured honeycomb-shaped mineralization in the matrix; an outcome that was previously shown to be indicative of late osteoblast/early osteocyte activity. This study highlights the potential of mechanical load to accelerate differentiation and enhance osteoblast communication and function during the differentiation process, and highlights a time point of cell differentiation within this scaffold to apply load in order to most effectively transduce a mechanical signal.
在体外开发一种可行且功能完备的骨支架,使其能够在体内存活并承受机械负荷,这需要了解骨祖细胞的细胞生物学,特别是它们在细胞分化和成熟过程中如何受到机械刺激的影响。在本研究中,使用改良的FlexCell板施加机械负荷,对接种未分化小鼠胚胎干细胞的I型胶原蛋白支架施加受限压缩。在分化的5至30天内,当细胞在有或没有施加机械负荷的情况下被刺激分化为成骨细胞时,检测成骨细胞钙黏蛋白(OB-Cad)和连接蛋白43的活性、存在情况和表达,以及各种多能性和成骨标记物。光漂白后的荧光恢复、免疫荧光、活力、冯·科萨染色和实时聚合酶链反应评估表明,这种接种细胞的支架的机械预刺激改变了OB-Cad和连接蛋白43的表达,并导致胶原蛋白基质中矿化的结构和组织存在显著差异。具体而言,在分化5天后加载40小时然后再完全分化30天的凝胶中的细胞,在基质中产生了高度结构化的蜂窝状矿化;先前的研究表明,这一结果表明存在晚期成骨细胞/早期骨细胞活性。本研究强调了机械负荷在分化过程中加速分化、增强成骨细胞通讯和功能的潜力,并突出了在该支架内细胞分化的一个时间点来施加负荷,以便最有效地转导机械信号。