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首页> 外文期刊>Molecules >Hemocyanin Modification of Chitosan Scaffolds with Calcium Phosphate Phases Increase the Osteoblast/Osteoclast Activity Ratio—A Co-Culture Study
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Hemocyanin Modification of Chitosan Scaffolds with Calcium Phosphate Phases Increase the Osteoblast/Osteoclast Activity Ratio—A Co-Culture Study

机译:用磷酸钙阶段改性壳聚糖支架的血晶素改变,增加了成骨细胞/破骨细胞活性比 - 一种共培养研究

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摘要

The ongoing research on biomaterials that support bone regeneration led to the quest formaterials or material modifications that can actively influence the activity or balance of bone tissuecells. The bone biocompatibility of porous chitosan scaffolds was modified in the present study bythe addition of calcium phosphates or hemocyanin. The first strategy comprised the incorporationof calcium phosphates into chitosan to create a biomimetic chitosan—mineral phase composite. Thesecond strategy comprised dip-coating of chitosan scaffolds with hemocyanin extracted fromcrayfish hemolymph. The cytocompatibility was assessed in a mono-culture of human bone marrowstromal cells (hBMSCs) and their differentiation to osteoblasts; in a mono-culture of humanmonocytes (hMs) and their maturation to osteoclasts; and in a co-culture of hBMSC/osteoblasts—hM/osteoclasts. Mineral incorporation caused an increase in scaffold bioactivity, as shown byreduced calcium concentration in the cell culture medium, delayed differentiation of hBMSCs, andreduced osteoclastic maturation of hMs in mono-culture. Dip-coating with hemocyanin led toincreased proliferation of hBMSCs and equivalent osteoclast maturation in mono-culture, while inco-culture, both an inhibitory effect of mineral incorporation on osteoblastogenesis and stimulatoryeffects of hemocyanin were observed. It was concluded that highly bioactive scaffolds (containingmineral phases) restrain osteoblast and osteoclast development, while hemocyanin coatingsignificantly supports osteoblastogenesis. These influences on the osteoblasts/osteoclasts activityratio may support scaffold-driven bone healing in the future.
机译:持续研究支持骨再生的生物材料导致Quest型材或材料修饰,可以积极影响骨组织的活动或平衡。通过加入磷酸钙或血红蛋白的本研究改进了多孔壳聚糖支架的骨生物相容性。第一种策略包括磷酸钙掺入壳聚糖,以产生仿生壳聚糖 - 矿物相复合物。第20次战略包括壳聚糖支架的浸涂,其中血红蛋白从血小瘤血淋巴中提取。在人骨髓细胞(HBMSCs)的单培养物中评估细胞膜相容性及其与成骨细胞的分化;在人甘蔗细胞(HMS)的单培养物中及其成熟的疏口细胞;在HBMSC /骨细胞-HM /骨粒细胞的共同培养中。矿物掺入导致支架生物活性的增加,如细胞培养基中的钙浓度所示,HBMSCs的延迟分化,单培养物中HMS的骨质细胞成熟成熟。用血红蛋白浸涂LED在单培养物中引起了HBMSCs和当量骨质体成熟的增殖,同时凝结培养,矿物质掺入对血红蛋白的骨细胞发生和刺激良好的影响。结论是,高度生物活跃的支架(含有氨阶段)抑制成骨细胞和骨质体发育,而血晶素涂层均可均可支持骨纤维发生。这些对成骨细胞/破骨细胞活性的影响可能在未来可以支持支架驱动的骨愈合。

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