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Effect of Nano-HA/Collagen Composite Hydrogels on Osteogenic Behavior of Mesenchymal Stromal Cells

机译:纳米HA /胶原复合水凝胶对间质基质细胞成骨行为的影响

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摘要

This study aimed to comparatively evaluate the in vitro effect of nanosized hydroxyapatite and collagen (nHA/COL) based composite hydrogels (with different ratios of nHA and COL) on the behavior of human mesenchymal stromal cells (MSCs), isolated from either adipose tissue (AT-MSCs) or bone marrow (BM-MSCs). We hypothesized that (i) nHA/COL composite hydrogels would promote the osteogenic differentiation of MSCs in an nHA concentration dependent manner, and that (ii) AT-MSCs would show higher osteogenic potential compared to BM-MSCs, due to their earlier observed higher proliferation and osteogenic differentiation potential in 2D in vitro cultures []. The obtained results indicated that AT-MSCs show indeed high proliferation, differentiation and mineralization capacities in nHA/COL constructs compared to BM-MSCs, but this effect was irrespective of nHA concentration. Based on the results of alkaline phosphatase (ALP) activity and osteocalcin (OCN) protein level, the osteogenic differentiation of BM-MSCs started in the beginning of the culture period and for AT-MSCs at the end of the culture period. At a molecular level, both cell types showed high expression of osteogenic markers (bone morphogenic protein 2 [BMP2], runt-related transcription factor 2 [RUNX2], OCN or COL1) in both an nHA concentration and time dependent manner. In conclusion, AT-MSCs demonstrated higher osteogenic potential in nHA/COL based 3D micro-environments compared to BM-MSCs, in which proliferation and osteogenic differentiation were highly promoted in a time dependent manner, irrespective of nHA amount in the constructs. The fact that AT-MSCs showed high proliferation and mineralization potential is appealing for their application in future pre-clinical research as an alternative cell source for BM-MSCs.
机译:这项研究旨在比较评估基于纳米羟基磷灰石和胶原(nHA / COL)的复合水凝胶(nHA和COL的比例不同)对从任一脂肪组织(MSC)分离的人间充质基质细胞(MSC)行为的体外影响。 AT-MSC)或骨髓(BM-MSC)。我们假设(i)nHA / COL复合水凝胶将以nHA浓度依赖性方式促进MSC的成骨分化,并且(ii)与BM-MSC相比,AT-MSC具有更高的成骨潜能,因为它们观察到的更高2D体外培养中的增殖和成骨分化潜能[]。获得的结果表明,与BM-MSC相比,AT-MSC在nHA / COL构建体中确实显示出高增殖,分化和矿化能力,但是这种作用与nHA浓度无关。根据碱性磷酸酶(ALP)活性和骨钙蛋白(OCN)蛋白水平的结果,BM-MSC的成骨分化始于培养期开始,而AT-MSC的成骨分化则始于培养期结束。在分子水平上,两种细胞类型均以nHA浓度和时间依赖性方式高表达成骨标记物(骨形态发生蛋白2 [BMP2],矮子相关转录因子2 [RUNX2],OCN或COL1)。总之,与基于BM-MSC的BM-MSC相比,AT-MSC在基于nHA / COL的3D微环境中显示出更高的成骨潜能,而不论构建物中的nHA量如何,增殖和成骨分化均以时间依赖性方式得到了促进。 AT-MSC具有高增殖和矿化潜力的事实吸引了它们在未来的临床前研究中作为BM-MSC的替代细胞来源的应用。

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