Yang Mingying, Shuai Yajun, Zhang Can, Chen Yuyin, Zhu Liangjun, Mao Chuanbin, OuYang Hongwei
Institute of Applied Bioresource Research, College of Animal Science, Zhejiang University , Yuhangtang Road 866, Hangzhou, 310058, China.
Biomacromolecules. 2014 Apr 14;15(4):1185-93. doi: 10.1021/bm401740x. Epub 2014 Mar 26.
Biomacromolecules have been used as templates to grow hydroxyapatite crystals (HAps) by biomineralization to fabricate mineralized materials for potential application in bone tissue engineering. Silk sericin is a protein with features desirable as a biomaterial, such as increased hydrophilicity and biodegradation. Mineralization of the silk sericin from Antheraea pernyi (A. pernyi) silkworm has rarely been reported. Here, for the first time, nucleation of HAps on A. pernyi silk sericin (AS) was attempted through a wet precipitation method and consequently the cell viability and osteogenic differentiation of BMSCs on mineralized AS were investigated. It was found that AS mediated the nucleation of HAps in the form of nanoneedles while self-assembling into β-sheet conformation, leading to the formation of a biomineralized protein based biomaterial. The cell viability assay of BMSCs showed that the mineralization of AS stimulated cell adhesion and proliferation, showing that the resultant AS biomaterial is biocompatible. The differentiation assay confirmed that the mineralized AS significantly promoted the osteogenic differentiation of BMSCs when compared to nonmineralized AS as well as other types of sericin (B. mori sericin), suggesting that the resultant mineralized AS biomaterial has potential in promoting bone formation. This result represented the first work proving the osteogenic differentiation of BMSCs directed by silk sericin. Therefore, the biomineralization of A. pernyi silk sericin coupled with seeding BMSCs on the resultant mineralized biomaterials is a useful strategy to develop the potential application of this unexplored silk sericin in the field of bone tissue engineering. This study lays the foundation for the use of A. pernyi silk sericin as a potential scaffold for tissue engineering.
生物大分子已被用作模板,通过生物矿化作用生长羟基磷灰石晶体(HAps),以制造矿化材料,用于骨组织工程的潜在应用。丝胶蛋白是一种具有作为生物材料所需特性的蛋白质,如亲水性增加和可生物降解性。关于柞蚕的丝胶蛋白矿化的报道很少。在此,首次尝试通过湿沉淀法使HAps在柞蚕丝胶蛋白(AS)上成核,并研究了矿化AS上骨髓间充质干细胞(BMSCs)的细胞活力和成骨分化。研究发现,AS以纳米针的形式介导HAps的成核,同时自组装成β-折叠构象,从而形成一种基于生物矿化蛋白的生物材料。BMSCs的细胞活力测定表明,AS的矿化刺激了细胞黏附和增殖,表明所得的AS生物材料具有生物相容性。分化测定证实,与未矿化的AS以及其他类型的丝胶蛋白(家蚕丝胶蛋白)相比,矿化的AS显著促进了BMSCs的成骨分化,这表明所得的矿化AS生物材料在促进骨形成方面具有潜力。这一结果代表了首次证明丝胶蛋白可引导BMSCs成骨分化的工作。因此,柞蚕丝胶蛋白的生物矿化以及在所得矿化生物材料上接种BMSCs是开发这种未被探索的丝胶蛋白在骨组织工程领域潜在应用的一种有用策略。本研究为将柞蚕丝胶蛋白用作组织工程的潜在支架奠定了基础。