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使用可生物降解支架在体外构建三维骨组织:研究初始细胞接种密度和培养时间。

Engineering three-dimensional bone tissue in vitro using biodegradable scaffolds: investigating initial cell-seeding density and culture period.

作者信息

Holy C E, Shoichet M S, Davies J E

机构信息

Institute for Biomaterials and BioMedical Engineering, University of Toronto, 170 College Street, Toronto, Ontario M5S 3E3, Canada.

出版信息

J Biomed Mater Res. 2000 Sep 5;51(3):376-82. doi: 10.1002/1097-4636(20000905)51:3<376::aid-jbm11>3.0.co;2-g.

Abstract

New three-dimensional (3D) scaffolds for bone tissue engineering have been developed throughout which bone cells grow, differentiate, and produce mineralized matrix. In this study, the percentage of cells anchoring to our polymer scaffolds as a function of initial cell seeding density was established; we then investigated bone tissue formation throughout our scaffolds as a function of initial cell seeding density and time in culture. Initial cell seeding densities ranging from 0.5 to 10 x 10(6) cells/cm(3) were seeded onto 3D scaffolds. After 1 h in culture, we determined that 25% of initial seeded cells had adhered to the scaffolds in static culture conditions. The cell-seeded scaffolds remained in culture for 3 and 6 weeks, to investigate the effect of initial cell seeding density on bone tissue formation in vitro. Further cultures using 1 x 10(6) cells/cm(3) were maintained for 1 h and 1, 2, 4, and 6 weeks to study bone tissue formation as a function of culture period. After 3 and 6 weeks in culture, scaffolds seeded with 1 x 10(6) cells/cm(3) showed similar tissue formation as those seeded with higher initial cell seeding densities. When initial cell seeding densities of 1 x 10(6) cells/cm(3) were used, osteocalcin immunolabeling indicative of osteoblast differentiation was seen throughout the scaffolds after only 2 weeks of culture. Von Kossa and tetracycline labeling, indicative of mineralization, occurred after 3 weeks. These results demonstrated that differentiated bone tissue was formed throughout 3D scaffolds after 2 weeks in culture using an optimized initial cell density, whereas mineralization of the tissue only occurred after 3 weeks. Furthermore, after 6 weeks in culture, newly formed bone tissue had replaced degrading polymer.

摘要

用于骨组织工程的新型三维(3D)支架已被开发出来,骨细胞可在其中生长、分化并产生矿化基质。在本研究中,确定了锚定在我们的聚合物支架上的细胞百分比与初始细胞接种密度的关系;然后,我们研究了在整个支架中骨组织形成与初始细胞接种密度和培养时间的关系。将初始细胞接种密度范围为0.5至10×10⁶个细胞/cm³的细胞接种到3D支架上。在培养1小时后,我们确定在静态培养条件下,25%的初始接种细胞已附着在支架上。接种细胞的支架在培养中持续3周和6周,以研究初始细胞接种密度对体外骨组织形成的影响。使用1×10⁶个细胞/cm³进行进一步培养,持续1小时以及1、2、4和6周,以研究骨组织形成与培养时间的关系。在培养3周和6周后,接种1×10⁶个细胞/cm³的支架显示出与接种更高初始细胞接种密度的支架相似的组织形成。当使用1×10⁶个细胞/cm³的初始细胞接种密度时,仅在培养2周后,在整个支架中就可见到指示成骨细胞分化的骨钙素免疫标记。指示矿化的冯·科萨染色和四环素标记在3周后出现。这些结果表明,在使用优化的初始细胞密度培养2周后,在整个3D支架中形成了分化的骨组织,而组织的矿化仅在3周后发生。此外,在培养6周后,新形成的骨组织取代了降解的聚合物。

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