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具有纳米晶体表面微观结构的可生物降解大孔支架用于高效骨生成和血管生成。

Biodegradable macroporous scaffold with nano-crystal surface microstructure for highly effective osteogenesis and vascularization.

作者信息

Chu Linyang, Jiang Guoqiang, Hu Xi-Le, James Tony D, He Xiao-Peng, Li Yaping, Tang Tingting

机构信息

Shanghai Key Laboratory of Orthopedic Implants, Department of Orthopedic Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, P. R. China.

出版信息

J Mater Chem B. 2018 Mar 21;6(11):1658-1667. doi: 10.1039/c7tb03353b. Epub 2018 Mar 1.

Abstract

Using the hydrothermal calcination method, bovine cancellous bone was transformed into a degradable macroporous scaffold with a nano-crystal surface microstructure, capable of releasing bioactive ions. Compared with the control group, the presence of the nano-crystal microstructure of the material scaffold significantly promoted the gene expression of adhesion proteins including integrin and vinculin, thus facilitating attachment, spreading, proliferation and focal adhesion formation of MC3T3-E1 cells on the surface of the scaffold. Additionally, the release of active magnesium and calcium ions from the scaffold promoted expression of osteogenic genes and formation of calcium nodules in osteoblasts. Both in vitro and in vivo assays demonstrated that the three-dimensional interconnected porous architecture promoted vascularization and tissue integration. Our findings provide new insight into the development of degradable macroporous composite materials with "three-dimensional" surface microstructures as bone substitutes or tissue engineering scaffolds with potential for clinical applications.

摘要

采用水热煅烧法,将牛松质骨转化为具有纳米晶体表面微观结构的可降解大孔支架,该支架能够释放生物活性离子。与对照组相比,材料支架的纳米晶体微观结构显著促进了包括整合素和纽蛋白在内的黏附蛋白的基因表达,从而促进了MC3T3-E1细胞在支架表面的附着、铺展、增殖和黏着斑形成。此外,支架中活性镁离子和钙离子的释放促进了成骨基因的表达和成骨细胞中钙结节的形成。体外和体内试验均表明,三维互连多孔结构促进了血管生成和组织整合。我们的研究结果为开发具有“三维”表面微观结构的可降解大孔复合材料作为骨替代物或具有临床应用潜力的组织工程支架提供了新的见解。

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