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骨形态发生蛋白-2 和原代成骨细胞在双相磷酸钙支架中诱导骨形成。

Induction of bone formation in biphasic calcium phosphate scaffolds by bone morphogenetic protein-2 and primary osteoblasts.

机构信息

Department of Plastic and Hand Surgery, University of Erlangen Medical Center, Friedrich-Alexander-University of Erlangen-Nürnberg, Germany.

出版信息

J Tissue Eng Regen Med. 2014 Mar;8(3):176-85. doi: 10.1002/term.1511. Epub 2012 Jun 28.

Abstract

Bone tissue engineering strategies mainly depend on porous scaffold materials. In this study, novel biphasic calcium phosphate (BCP) matrices were generated by 3D-printing. High porosity was achieved by starch consolidation. This study aimed to characterise the porous BCP-scaffold properties and interactions of osteogenic cells and growth factors under in vivo conditions. Five differently treated constructs were implanted subcutaneously in syngeneic rats: plain BCP constructs (group A), constructs pre-treated with BMP-2 (group B; 1.6 µg BMP-2 per scaffold), seeded with primary osteoblasts (OB) (group C), seeded with OB and BMP-2 (group D) and constructs seeded with OB and pre-cultivated in a flow bioreactor for 6 weeks (group E). After 2, 4 and 6 weeks, specimens were explanted and subjected to histological and molecular biological analyses. Explanted scaffolds were invaded by fibrovascular tissue without significant foreign body reactions. Morphometric analysis demonstrated significantly increased bone formation in samples from group D (OB + BMP-2) compared to all other groups. Samples from groups B-E displayed significant mRNA expression of bone-specific genes after 6 weeks. Pre-cultivation in the flow bioreactor (group E) induced bone formation comparable with group B. In this study, differences in bone distribution between samples with BMP-2 or osteoblasts could be observed. In conclusion, combination of osteoblasts and BMP-2 synergistically enhanced bone formation in novel ceramic scaffolds. These results provide the basis for further experiments in orthotopic defect models with a focus on future applications in orthopaedic and reconstructive surgery.

摘要

骨组织工程策略主要依赖于多孔支架材料。本研究通过 3D 打印生成新型双相磷酸钙(BCP)基质。通过淀粉固结实现高孔隙率。本研究旨在对多孔 BCP 支架的特性以及成骨细胞和生长因子在体内条件下的相互作用进行研究。将五种不同处理的构建体植入同基因大鼠的皮下:普通 BCP 构建体(A 组)、用 BMP-2 预处理的构建体(B 组;每个支架 1.6μg BMP-2)、接种原代成骨细胞(OB)的构建体(C 组)、接种 OB 和 BMP-2 的构建体(D 组)以及接种 OB 并在流控生物反应器中预培养 6 周的构建体(E 组)。在 2、4 和 6 周后,取出标本进行组织学和分子生物学分析。植入的支架被纤维血管组织侵袭,但没有明显的异物反应。形态计量分析显示,D 组(OB+BMP-2)的骨形成明显高于其他组。在第 6 周,B-E 组的样本均显示出骨特异性基因的显著 mRNA 表达。在流控生物反应器中的预培养(E 组)诱导的骨形成与 B 组相当。在这项研究中,可以观察到有 BMP-2 或成骨细胞的样本之间的骨分布差异。总之,成骨细胞和 BMP-2 的联合使用可以协同增强新型陶瓷支架中的骨形成。这些结果为进一步在骨缺损模型中进行实验提供了基础,重点是在骨科和重建外科中的未来应用。

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