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生物反应器培养时间影响间充质干细胞构建工程的骨形成。

Bioreactor culture duration of engineered constructs influences bone formation by mesenchymal stem cells.

机构信息

Department of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA.

Department of Biomedical Engineering, University of California, Davis, Davis, CA 95616, USA; Department of Orthopaedic Surgery, School of Medicine, University of California, Davis, Sacramento, CA 95817, USA.

出版信息

Biomaterials. 2017 Nov;146:29-39. doi: 10.1016/j.biomaterials.2017.08.044. Epub 2017 Sep 6.

Abstract

Perfusion culture of mesenchymal stem cells (MSCs) seeded in biomaterial scaffolds provides nutrients for cell survival, enhances extracellular matrix deposition, and increases osteogenic cell differentiation. However, there is no consensus on the appropriate perfusion duration of cellular constructs in vitro to boost their bone forming capacity in vivo. We investigated this phenomenon by culturing human MSCs in macroporous composite scaffolds in a direct perfusion bioreactor and compared their response to scaffolds in continuous dynamic culture conditions on an XYZ shaker. Cell seeding in continuous perfusion bioreactors resulted in more uniform MSC distribution than static seeding. We observed similar calcium deposition in all composite scaffolds over 21 days of bioreactor culture, regardless of pore size. Compared to scaffolds in dynamic culture, perfused scaffolds exhibited increased DNA content and expression of osteogenic markers up to 14 days in culture that plateaued thereafter. We then evaluated the effect of perfusion culture duration on bone formation when MSC-seeded scaffolds were implanted in a murine ectopic site. Human MSCs persisted in all scaffolds at 2 weeks in vivo, and we observed increased neovascularization in constructs cultured under perfusion for 7 days relative to those cultured for 1 day within each gender. At 8 weeks post-implantation, we observed greater bone volume fraction, bone mineral density, tissue ingrowth, collagen density, and osteoblastic markers in bioreactor constructs cultured for 14 days compared to those cultured for 1 or 7 days, and acellular constructs. Taken together, these data demonstrate that culturing MSCs under perfusion culture for at least 14 days in vitro improves the quantity and quality of bone formation in vivo. This study highlights the need for optimizing in vitro bioreactor culture duration of engineered constructs to achieve the desired level of bone formation.

摘要

将间质干细胞(MSCs)种植在生物材料支架中的灌注培养为细胞存活提供了营养,增强了细胞外基质的沉积,并增加了成骨细胞的分化。然而,对于体外细胞构建物的适当灌注持续时间以提高其体内成骨能力,尚无共识。我们通过在直接灌注生物反应器中培养人 MSCs 来研究这种现象,并将其与在 XYZ 摇床上进行连续动态培养条件下的支架进行比较。与静态接种相比,在连续灌注生物反应器中接种可使 MSC 分布更加均匀。我们观察到在生物反应器培养的 21 天内,所有复合支架中的钙沉积相似,与孔径无关。与动态培养的支架相比,灌注支架在培养的前 14 天内表现出更高的 DNA 含量和更高的成骨标志物表达,此后达到平台期。然后,我们评估了在 MSC 接种支架植入小鼠异位部位时灌注培养持续时间对骨形成的影响。在体内 2 周时,所有支架中均存在人 MSCs,我们观察到在灌注培养 7 天时与培养 1 天时相比,构建物中的新生血管化增加。在植入后 8 周时,与培养 1 天或 7 天相比,培养 14 天的生物反应器构建物具有更大的骨体积分数、骨密度、组织内生长、胶原密度和成骨标志物,而无细胞构建物则没有。总之,这些数据表明,在体外灌注培养至少 14 天可以提高体内成骨的数量和质量。这项研究强调了需要优化工程构建物的体外生物反应器培养持续时间,以达到预期的成骨水平。

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