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Effects of Cellular Parameters on the In Vitro Osteogenic Potential of Dual-Gelling Mesenchymal Stem Cell-Laden Hydrogels

机译:细胞参数对双凝胶间充质干细胞载水凝胶体外成骨潜能的影响

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摘要

This work investigated the effects of cellular encapsulation density and differentiation stage on the osteogenic capacity of injectable, dual physically and chemically gelling hydrogels comprised of thermogelling macromers and polyamidoamine crosslinkers. Undifferentiated and osteogenically predifferentiated mesenchymal stem cells (MSCs) were encapsulated within 20 wt% composite hydrogels with gelatin microparticles at densities of 6 or 15 million cells/mL. We hypothesized that a high encapsulation density and predifferentiation would promote increased cellular interaction and accelerate osteogenesis, leading to enhanced osteogenic potential in vitro. Hydrogels were able to maintain the viability of the encapsulated cells over a period of 28 days, with the high encapsulation density and predifferentiation group possessing the highest DNA content at all timepoints. Early alkaline phosphatase activity and mineralization were promoted by encapsulation density, whereas this effect by predifferentiation was only observed in the low seeding density groups. Both parameters only demonstrated short-lived effects when examined independently, but jointly led to greater levels of alkaline phosphatase activity and mineralization. The combined effects suggest that there may be optimal encapsulation densities and differentiation periods that need to be investigated to improve MSCs for biomaterials-based therapeutics in bone tissue engineering.
机译:这项工作研究了细胞包封密度和分化阶段对由热凝胶大分子单体和聚酰胺酰胺交联剂组成的可注射,物理和化学双重凝胶化水凝胶的成骨能力的影响。将未分化和成骨前分化的间充质干细胞(MSCs)封装在含有明胶微粒的20 wt%复合水凝胶中,密度为6或1500万个细胞/ mL。我们假设高封装密度和预分化将促进增加的细胞相互作用并加速成骨作用,从而导致体外增强成骨潜力。水凝胶能够在28天的时间内保持被封装细胞的活力,其中高封装密度和预分化组在所有时间点均具有最高的DNA含量。包囊密度促进了早期碱性磷酸酶的活性和矿化作用,而仅在低播种密度组中观察到了预分化作用。当独立检查时,这两个参数仅表现出短暂的作用,但共同导致更高水平的碱性磷酸酶活性和矿化作用。综合的影响表明,可能需要最佳的包囊密度和分化期,以改善MSC,以改善骨组织工程中基于生物材料的治疗方法。

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