首页> 美国卫生研究院文献>Molecules >Hemocyanin Modification of Chitosan Scaffolds with Calcium Phosphate Phases Increase the Osteoblast/Osteoclast Activity Ratio—A Co-Culture Study
【2h】

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

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The ongoing research on biomaterials that support bone regeneration led to the quest for materials or material modifications that can actively influence the activity or balance of bone tissue cells. The bone biocompatibility of porous chitosan scaffolds was modified in the present study by the addition of calcium phosphates or hemocyanin. The first strategy comprised the incorporation of calcium phosphates into chitosan to create a biomimetic chitosan—mineral phase composite. The second strategy comprised dip-coating of chitosan scaffolds with hemocyanin extracted from crayfish hemolymph. The cytocompatibility was assessed in a mono-culture of human bone marrow stromal cells (hBMSCs) and their differentiation to osteoblasts; in a mono-culture of human monocytes (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 by reduced calcium concentration in the cell culture medium, delayed differentiation of hBMSCs, and reduced osteoclastic maturation of hMs in mono-culture. Dip-coating with hemocyanin led to increased proliferation of hBMSCs and equivalent osteoclast maturation in mono-culture, while in co-culture, both an inhibitory effect of mineral incorporation on osteoblastogenesis and stimulatory effects of hemocyanin were observed. It was concluded that highly bioactive scaffolds (containing mineral phases) restrain osteoblast and osteoclast development, while hemocyanin coating significantly supports osteoblastogenesis. These influences on the osteoblasts/osteoclasts activity ratio 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探索可以积极影响骨组织细胞的活性或平衡的材料或材料修饰。通过添加磷酸钙或血红蛋白在本研究中改性多孔壳聚糖支架的骨生物相容性。第一策略包括将磷酸钙掺入壳聚糖中以产生仿生壳聚糖 - 矿物相复合物。第二次策略包括用从小龙虾血淋巴中提取的血糖蛋白浸涂的壳聚糖支架。在人骨髓基质细胞(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;在人单核细胞(HMS)的单培养物中及其对骨质体的成熟;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降低,HBMSCs的延迟分化和单培养物中HMS的降低的骨质细胞组织成熟。用血糖蛋白浸涂导致单培养物中HBMSCs和等同的骨质体成熟的增加,而在共培养中,观察到矿物质掺入对血红蛋白的骨细胞发生和刺激作用的抑制作用。结论是,高度生物活跃的支架(含矿物阶段)抑制成骨细胞和破骨细胞发育,而血糖素涂层显着支持骨纤维细胞发生。这些对成骨细胞/破骨细胞活性比的影响可能在未来支持支架驱动的骨愈合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号