Research Center for Experimental Orthopaedics, Heidelberg University Hospital, 69118, Heidelberg, Germany.
Clinic for Orthopaedics and Trauma Surgery, Heidelberg University Hospital, 69118, Heidelberg, Germany.
J Biomed Mater Res B Appl Biomater. 2018 Aug;106(6):2214-2224. doi: 10.1002/jbm.b.34027. Epub 2017 Oct 25.
Tissue engineering approaches for reconstructing full-depth cartilage defects need to comprise a zone of calcified cartilage to tightly anchor cartilage constructs into the subchondral bone. Here, we investigated whether growth and differentiation factor-5-(GDF-5)-augmented fibrin hydrogel can induce a calcified cartilage-layer in vitro that seamlessly connects cartilage-relevant biomaterials with bone tissue. Human bone marrow stromal cells (BMSCs) were embedded in fibrin hydrogel and subjected to chondrogenesis with TGF-β with or without GDF-5 before constructs were implanted subcutaneously into SCID mice. A novel layered ectopic in vivo model was developed and GDF-5-augmented fibrin with BMSCs was used to glue hydrogel and collagen constructs onto bone disks to investigate formation of a calcified cartilage connecting zone. GDF-5 significantly enhanced ALP activity during in vitro chondrogenesis while ACAN and COL2A1 mRNA, proteoglycan-, collagen-type-II- and collagen-type-X-deposition remained similar to controls. Pellets pretreated with GDF-5 mineralized faster in vivo and formed more ectopic bone. In the novel layered ectopic model, GDF-5 strongly supported calcified cartilage formation that seamlessly connected with the bone. Pro-chondrogenic and pro-hypertrophic activity makes GDF-5-augmented fibrin an attractive bioactive hydrogel with high potential to stimulate a calcified cartilage connecting zone in situ that might promote integration of cartilage scaffolds with bone. Thus, GDF-5-augmented fibrin hydrogel promises to overcome poor fixation of biomaterials in cartilage defects facilitating their long-term regeneration. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2214-2224, 2018.
组织工程方法重建全层软骨缺损需要包括钙化软骨区,以将软骨构建物紧密锚定到软骨下骨中。在这里,我们研究了生长分化因子 5(GDF-5)增强的纤维蛋白水凝胶是否可以在体外诱导形成连续的软骨相关生物材料与骨组织的钙化软骨层。人骨髓基质细胞(BMSCs)嵌入纤维蛋白水凝胶中,并在 TGF-β存在或不存在 GDF-5 的情况下进行软骨生成,然后将构建物植入 SCID 小鼠的皮下。开发了一种新型分层异位体内模型,并使用 GDF-5 增强的纤维蛋白和 BMSCs 将水凝胶和胶原构建物粘接到骨盘上,以研究形成连续的钙化软骨连接区。GDF-5 显著增强了体外软骨生成过程中的碱性磷酸酶活性,而 ACAN 和 COL2A1mRNA、蛋白聚糖、Ⅱ型胶原和 X 型胶原的沉积与对照组相似。用 GDF-5 预处理的小球在体内矿化更快,形成更多的异位骨。在新型分层异位模型中,GDF-5 强烈支持钙化软骨的形成,与骨无缝连接。促软骨生成和促肥大活性使 GDF-5 增强的纤维蛋白成为一种有吸引力的生物活性水凝胶,具有很强的刺激原位钙化软骨连接区的潜力,这可能促进软骨支架与骨的整合。因此,GDF-5 增强的纤维蛋白水凝胶有望克服生物材料在软骨缺损中的固定不良问题,从而促进其长期再生。©2017 Wiley Periodicals,Inc. J Biomed Mater Res Part B:Appl Biomater,106B:2214-2224,2018。