Tuning Mesenchymal Stem Cell Response onto Titanium–Niobium–Hafnium Alloy by Recombinant Fibronectin Fragments

纤维连接蛋白 重组DNA 间充质干细胞 硅烷化 材料科学 碱性磷酸酶 细胞粘附 细胞培养 生物物理学 生物化学 分子生物学 细胞 化学 生物 细胞生物学 基因 复合材料 遗传学
作者
Carolina Herranz-Diez,Carlos Mas‐Moruno,Stefanie Neubauer,Horst Kessler,F.J. Gil,Marta Pegueroles,José María Manero,Jordi Guillem‐Marti
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:8 (4): 2517-2525 被引量:35
标识
DOI:10.1021/acsami.5b09576
摘要

Since metallic biomaterials used for bone replacement possess low bioactivity, the use of cell adhesive moieties is a common strategy to improve cellular response onto these surfaces. In recent years, the use of recombinant proteins has emerged as an alternative to native proteins and short peptides owing to the fact that they retain the biological potency of native proteins, while improving their stability. In the present study, we investigated the biological effect of two different recombinant fragments of fibronectin, spanning the 8-10th and 12-14th type III repeats, covalently attached to a new TiNbHf alloy using APTES silanization. The fragments were studied separately and mixed at different concentrations and compared to a linear RGD, a cyclic RGD and the full-length fibronectin protein. Cell culture studies using rat mesenchymal stem cells demonstrated that low to medium concentrations (30% and 50%) of type III 8-10th fragment mixed with type III 12-14th fragment stimulated cell spreading and proliferation compared to RGD peptides and the fragments separately. On the other hand, type III 12-14th fragment alone or mixed at low volume percentages ≤50% with type III 8-10th fragment increased alkaline phosphatase levels compared to the other molecules. These results are significant for the understanding of the role of fibronectin recombinant fragments in cell responses and thus to design bioactive coatings for biomedical applications.
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